ClinVar for MedGen (Select 322999) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3064552	NM_024996.7(GFM1):c.1764+2T>C	GFM1 (V589A)	Single nucleotide variant (missense variant +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2689126	NM_024996.7(GFM1):c.1396T>C (p.Phe466Leu)	GFM1 (F238L +7 more)	Single nucleotide variant (missense variant +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GUncertain significance
Select item 2675920	NM_024996.7(GFM1):c.974del (p.Asn325fs)	GFM1 (N136fs +6 more)	Deletion (frameshift variant +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 +1 more	GPathogenic/Likely pathogenic
Select item 2675919	NM_024996.7(GFM1):c.1981C>T (p.Gln661Ter)	GFM1 (Q433* +7 more)	Single nucleotide variant (nonsense +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675918	NM_024996.7(GFM1):c.636del (p.Gly213fs)	GFM1 (G138fs +2 more)	Deletion (intron variant +2 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675917	NM_024996.7(GFM1):c.324C>G (p.Tyr108Ter)	GFM1 (Y108* +1 more)	Single nucleotide variant (nonsense +2 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675916	NM_024996.7(GFM1):c.361dup (p.Thr121fs)	GFM1 (T121fs +1 more)	Duplication (frameshift variant +2 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675915	NM_024996.7(GFM1):c.1799del (p.Ser600fs)	GFM1 (S372fs +7 more)	Deletion (frameshift variant +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675914	NM_024996.7(GFM1):c.689+2T>C	GFM1	Single nucleotide variant (splice donor variant +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675913	NM_024996.7(GFM1):c.527T>A (p.Leu176Ter)	GFM1 (L101* +1 more)	Single nucleotide variant (nonsense +2 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675912	NM_024996.7(GFM1):c.1303dup (p.Ala435fs)	GFM1 (A207fs +7 more)	Duplication (frameshift variant +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675911	NM_024996.7(GFM1):c.725T>G (p.Leu242Ter)	GFM1 (L14* +6 more)	Single nucleotide variant (nonsense +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 +1 more	GPathogenic/Likely pathogenic
Select item 2675910	NM_024996.7(GFM1):c.1951del (p.Ala651fs)	GFM1 (A423fs +7 more)	Deletion (frameshift variant +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675909	NM_024996.7(GFM1):c.114_115del (p.Val40fs)	GFM1 (V40fs)	Deletion (frameshift variant +2 more)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 2675908	NM_024996.7(GFM1):c.999-1G>C	GFM1	Single nucleotide variant (splice acceptor variant)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675907	NM_024996.7(GFM1):c.113_116dup (p.Val40fs)	GFM1 (V40fs)	Duplication (frameshift variant +2 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675906	NM_024996.7(GFM1):c.1157dup (p.Asn386fs)	GFM1 (N158fs +6 more)	Duplication (frameshift variant +2 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675905	NM_024996.7(GFM1):c.381del (p.Phe127fs)	GFM1 (F127fs +1 more)	Deletion (frameshift variant +2 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675904	NM_024996.7(GFM1):c.1381-1G>C	GFM1	Single nucleotide variant (splice acceptor variant)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675903	NM_024996.7(GFM1):c.929T>G (p.Leu310Ter)	GFM1 (L121* +6 more)	Single nucleotide variant (nonsense +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675902	NM_024996.7(GFM1):c.909del (p.Asn303fs)	GFM1 (N114fs +6 more)	Deletion (frameshift variant +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675901	NM_024996.7(GFM1):c.362_367delinsTT (p.Thr121fs)	GFM1 (T121fs +1 more)	Indel (frameshift variant +2 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675900	NM_024996.7(GFM1):c.368-2A>C	GFM1	Single nucleotide variant (splice acceptor variant +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675899	NM_024996.7(GFM1):c.154_155del (p.Ala53fs)	GFM1 (A53fs)	Microsatellite (frameshift variant +2 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675897	NM_024996.7(GFM1):c.136del (p.Ile46fs)	GFM1 (I46fs)	Deletion (frameshift variant +2 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675896	NM_024996.7(GFM1):c.573-2A>G	GFM1	Single nucleotide variant (splice acceptor variant +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675895	NM_024996.7(GFM1):c.1193T>C (p.Leu398Pro)	GFM1 (L170P +6 more)	Single nucleotide variant (missense variant +2 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675894	NM_024996.7(GFM1):c.579dup (p.Leu194fs)	GFM1 (L119fs +2 more)	Duplication (frameshift variant +2 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675893	NM_024996.7(GFM1):c.705T>G (p.Tyr235Ter)	GFM1 (Y160* +6 more)	Single nucleotide variant (nonsense +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675892	NM_024996.7(GFM1):c.1909+2T>A	GFM1	Single nucleotide variant (splice donor variant)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675891	NM_024996.7(GFM1):c.626del (p.Gly209fs)	GFM1 (G134fs +2 more)	Deletion (frameshift variant +2 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675890	NM_024996.7(GFM1):c.787C>T (p.Gln263Ter)	GFM1 (Q110* +6 more)	Single nucleotide variant (nonsense +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 +1 more	GPathogenic/Likely pathogenic
Select item 2675889	NM_024996.7(GFM1):c.914del (p.Gly305fs)	GFM1 (G116fs +6 more)	Deletion (frameshift variant +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GPathogenic
Select item 2675888	NM_024996.7(GFM1):c.1044_1056del (p.Asn349fs)	GFM1 (N121fs +6 more)	Deletion (frameshift variant +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675887	NM_024996.7(GFM1):c.367+1G>A	GFM1	Single nucleotide variant (splice donor variant +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675886	NM_024996.7(GFM1):c.1516C>T (p.Gln506Ter)	GFM1 (Q278* +7 more)	Single nucleotide variant (nonsense +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2675885	NM_024996.7(GFM1):c.1905_1908del (p.Gln636fs)	GFM1 (Q408fs +7 more)	Deletion (frameshift variant +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 2585025	NM_024996.7(GFM1):c.152T>G (p.Ile51Ser)	GFM1 (I51S)	Single nucleotide variant (missense variant +2 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GUncertain significance
Select item 2444405	NM_024996.7(GFM1):c.679G>A (p.Gly227Arg)	GFM1 (G152R +2 more)	Single nucleotide variant (missense variant +2 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GUncertain significance
Select item 2442220	NM_024996.7(GFM1):c.575C>A (p.Ser192Tyr)	GFM1 (S117Y +2 more)	Single nucleotide variant (missense variant +2 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GUncertain significance
Select item 2441883	NM_024996.7(GFM1):c.754G>A (p.Glu252Lys)	GFM1 (E177K +6 more)	Single nucleotide variant (missense variant +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GUncertain significance
Select item 2432117	NM_024996.7(GFM1):c.1209C>A (p.Ala403=)	GFM1	Single nucleotide variant (synonymous variant +2 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GUncertain significance
Select item 2432116	NM_024996.7(GFM1):c.830C>T (p.Ser277Phe)	GFM1 (S124F +6 more)	Single nucleotide variant (missense variant +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GUncertain significance
Select item 2421099	NM_024996.7(GFM1):c.114del (p.Gly39_Val40insTer)	GFM1	Deletion (frameshift variant +2 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2187939	NM_024996.7(GFM1):c.1424del (p.Arg475fs)	GFM1 (R247fs +7 more)	Deletion (frameshift variant +1 more)	not provided +2 more	GPathogenic/Likely pathogenic
Select item 2162487	NM_024996.7(GFM1):c.1632dup (p.Gly545fs)	GFM1 (G564fs +7 more)	Duplication (frameshift variant +1 more)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 2150047	NM_024996.7(GFM1):c.368-2A>G	GFM1	Single nucleotide variant (splice acceptor variant +1 more)	not provided +1 more	GLikely pathogenic
Select item 2148396	NM_024996.7(GFM1):c.1380+2T>G	GFM1	Single nucleotide variant (splice donor variant)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 +1 more	GLikely pathogenic
Select item 1944995	NM_024996.7(GFM1):c.817dup (p.Ile273fs)	GFM1 (I292fs +6 more)	Duplication (frameshift variant +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 +1 more	GPathogenic
Select item 1802981	NM_024996.7(GFM1):c.2167T>C (p.Cys723Arg)	GFM1 (C495R +8 more)	Single nucleotide variant (missense variant +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 1802271	NM_024996.7(GFM1):c.1897G>C (p.Ala633Pro)	GFM1 (A405P +7 more)	Single nucleotide variant (missense variant +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GUncertain significance
Select item 1469533	NM_024996.7(GFM1):c.1765-2A>G	GFM1	Single nucleotide variant (splice acceptor variant)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 +1 more	GLikely pathogenic
Select item 1460386	NM_024996.7(GFM1):c.1186C>T (p.Gln396Ter)	GFM1 (Q357* +6 more)	Single nucleotide variant (nonsense +2 more)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 1456973	NM_024996.7(GFM1):c.89_99del (p.Trp30fs)	GFM1 (W30fs)	Deletion (frameshift variant +2 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 +1 more	GPathogenic/Likely pathogenic
Select item 1455901	NM_024996.7(GFM1):c.1532_1533del (p.Glu511fs)	GFM1 (E322fs +7 more)	Microsatellite (frameshift variant +1 more)	See cases +2 more	GPathogenic/Likely pathogenic
Select item 1455378	NM_024996.7(GFM1):c.532C>T (p.Arg178Ter)	GFM1 (R178* +1 more)	Single nucleotide variant (nonsense +2 more)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 1454007	NM_024996.7(GFM1):c.69G>A (p.Trp23Ter)	GFM1 (W23*)	Single nucleotide variant (nonsense +2 more)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 1453256	NM_024996.7(GFM1):c.850C>T (p.Arg284Ter)	GFM1 (R131* +6 more)	Single nucleotide variant (nonsense +1 more)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 1453055	NM_024996.7(GFM1):c.1882C>T (p.Arg628Ter)	GFM1 (R439* +7 more)	Single nucleotide variant (nonsense +1 more)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 1425853	NM_024996.7(GFM1):c.1172del (p.Lys391fs)	GFM1 (K163fs +6 more)	Deletion (non-coding transcript variant +2 more)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 1367819	NM_024996.7(GFM1):c.690_693del	GFM1	Deletion (splice acceptor variant)	GFM1-related disorder +2 more	GPathogenic/Likely pathogenic
Select item 1346304	NM_024996.7(GFM1):c.689+1G>A	GFM1	Single nucleotide variant (splice donor variant +1 more)	not provided +1 more	GLikely pathogenic
Select item 1322995	NM_024996.7(GFM1):c.1510del (p.Tyr504fs)	GFM1 (Y276fs +7 more)	Deletion (frameshift variant +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GPathogenic
Select item 1254017	NM_024996.7(GFM1):c.2143A>G (p.Met715Val)	GFM1 (M487V +8 more)	Single nucleotide variant (missense variant +1 more)	not provided	GConflicting classifications of pathogenicity
Select item 1210416	NM_024996.7(GFM1):c.748del (p.Arg250fs)	GFM1 (R175fs +6 more)	Deletion (frameshift variant +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GLikely pathogenic
Select item 1199313	NM_024996.7(GFM1):c.344A>G (p.Asn115Ser)	GFM1 (N115S +1 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases +2 more	GConflicting classifications of pathogenicity
Select item 1195558	NM_024996.7(GFM1):c.1256C>T (p.Ala419Val)	GFM1 (A191V +7 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1185267	NM_024996.7(GFM1):c.1519-25A>G	GFM1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1185266	NM_024996.7(GFM1):c.1323+72A>G	GFM1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1185265	NM_024996.7(GFM1):c.1083+82T>C	GFM1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1185264	NM_024996.7(GFM1):c.1083+57C>T	GFM1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1185263	NM_024996.7(GFM1):c.690-87A>G	GFM1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1185262	NM_024996.7(GFM1):c.689+891C>T	GFM1 (R245C)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 1185261	NM_024996.7(GFM1):c.81+84C>G	GFM1	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GBenign
Select item 1185260	NM_024996.7(GFM1):c.81+22A>G	GFM1	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GBenign
Select item 1142296	NM_024996.7(GFM1):c.1383C>T (p.Asn461=)	GFM1	Single nucleotide variant (synonymous variant +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 +1 more	GConflicting classifications of pathogenicity
Select item 1120022	NM_024996.7(GFM1):c.409G>A (p.Val137Met)	GFM1 (V137M +1 more)	Single nucleotide variant (missense variant +2 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GPathogenic
Select item 1119996	NM_024996.7(GFM1):c.1823G>A (p.Arg608Gln)	GFM1 (R380Q +7 more)	Single nucleotide variant (missense variant +1 more)	not provided	GPathogenic
Select item 1075664	NM_024996.7(GFM1):c.1090C>T (p.Arg364Ter)	GFM1 (R136* +6 more)	Single nucleotide variant (nonsense +2 more)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 1069701	NM_024996.7(GFM1):c.1576C>T (p.Arg526Ter)	GFM1 (R298* +7 more)	Single nucleotide variant (nonsense +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 +1 more	GPathogenic
Select item 1068183	NM_024996.7(GFM1):c.573-1G>C	GFM1	Single nucleotide variant (splice acceptor variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1067176	NM_024996.7(GFM1):c.81+1G>A	GFM1	Single nucleotide variant (5 prime UTR variant +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 +1 more	GLikely pathogenic
Select item 1066726	NM_024996.7(GFM1):c.999-1G>A	GFM1	Single nucleotide variant (splice acceptor variant)	not provided	GLikely pathogenic
Select item 1066690	NM_024996.7(GFM1):c.1910-2A>T	GFM1	Single nucleotide variant (splice acceptor variant)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 +1 more	GLikely pathogenic
Select item 1028358	NM_024996.7(GFM1):c.408A>T (p.Arg136Ser)	GFM1 (R61S +1 more)	Single nucleotide variant (missense variant +2 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GUncertain significance
Select item 1028357	NM_024996.7(GFM1):c.1324G>T (p.Glu442Ter)	GFM1 (E415* +7 more)	Single nucleotide variant (nonsense +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GPathogenic
Select item 1028356	NM_024996.7(GFM1):c.1221+20G>A	GFM1	Single nucleotide variant (intron variant)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 +1 more	GConflicting classifications of pathogenicity
Select item 991779	NM_024996.7(GFM1):c.1198C>T (p.Arg400Cys)	GFM1 (R172C +6 more)	Single nucleotide variant (missense variant +2 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 +1 more	GUncertain significance
Select item 991778	NM_024996.7(GFM1):c.825G>A (p.Ser275=)	GFM1	Single nucleotide variant (synonymous variant +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GUncertain significance
Select item 991777	NM_024996.7(GFM1):c.616G>T (p.Gly206Cys)	GFM1 (G131C +2 more)	Single nucleotide variant (missense variant +2 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GUncertain significance
Select item 991776	NM_024996.7(GFM1):c.443T>C (p.Val148Ala)	GFM1 (V148A +1 more)	Single nucleotide variant (missense variant +2 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 +1 more	GUncertain significance
Select item 991775	NM_024996.7(GFM1):c.221C>G (p.Ala74Gly)	GFM1 (A74G)	Single nucleotide variant (missense variant +2 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GUncertain significance
Select item 966719	NM_024996.7(GFM1):c.1180C>T (p.Arg394Trp)	GFM1 (R241W +6 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 951478	NM_024996.7(GFM1):c.1765-2_1765-1del	GFM1	Deletion (splice acceptor variant)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 +1 more	GPathogenic
Select item 940515	NM_024996.7(GFM1):c.1601+1G>A	GFM1	Single nucleotide variant (splice donor variant)	not provided +1 more	GLikely pathogenic
Select item 939719	NM_024996.7(GFM1):c.997_998+2del	GFM1	Deletion (splice donor variant)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 +1 more	GLikely pathogenic
Select item 936188	NM_024996.7(GFM1):c.247_248del (p.Asp83fs)	GFM1 (D83fs +1 more)	Deletion (frameshift variant +2 more)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 931966	NM_024996.7(GFM1):c.881C>T (p.Pro294Leu)	GFM1 (P313L +6 more)	Single nucleotide variant (missense variant +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GUncertain significance
Select item 930333	NM_024996.7(GFM1):c.607A>G (p.Ile203Val)	GFM1 (I14V +2 more)	Single nucleotide variant (missense variant +2 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GUncertain significance
Select item 902834	NM_024996.7(GFM1):c.*164C>A	GFM1	Single nucleotide variant (3 prime UTR variant +1 more)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GUncertain significance

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