ClinVar for Gene (Select 23171) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3062708	GRCh37/hg19 3p26.3-22.3(chr3:61891-33946644)x3	OXTR, PDCD6IP +145 more	Copy number gain	not specified	GPathogenic
Select item 3022935	NM_015141.4(GPD1L):c.675C>G (p.Thr225=)	GPD1L	Single nucleotide variant (synonymous variant)	Brugada syndrome	GLikely benign
Select item 3021841	NM_015141.4(GPD1L):c.828C>A (p.Ala276=)	GPD1L	Single nucleotide variant (synonymous variant)	Brugada syndrome	GLikely benign
Select item 3019672	NM_015141.4(GPD1L):c.618+15_618+16del	GPD1L	Deletion (intron variant)	Brugada syndrome	GLikely benign
Select item 3018661	NM_015141.4(GPD1L):c.366+7C>T	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome	GLikely benign
Select item 3017539	NM_015141.4(GPD1L):c.366+13C>A	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome	GLikely benign
Select item 2996158	NM_015141.4(GPD1L):c.426G>A (p.Met142Ile)	GPD1L (M142I)	Single nucleotide variant (missense variant)	Brugada syndrome	GUncertain significance
Select item 2988349	NM_015141.4(GPD1L):c.414C>G (p.Ile138Met)	GPD1L (I138M)	Single nucleotide variant (missense variant)	Brugada syndrome	GUncertain significance
Select item 2986847	NM_015141.4(GPD1L):c.1050T>C (p.His350=)	GPD1L	Single nucleotide variant (synonymous variant)	Brugada syndrome	GLikely benign
Select item 2955446	NM_015141.4(GPD1L):c.9G>A (p.Ala3=)	GPD1L, LOC129936414	Single nucleotide variant (synonymous variant)	Brugada syndrome	GLikely benign
Select item 2920561	NM_015141.4(GPD1L):c.929G>T (p.Arg310Leu)	GPD1L (R310L)	Single nucleotide variant (missense variant)	Brugada syndrome	GUncertain significance
Select item 2918323	NM_015141.4(GPD1L):c.483G>A (p.Glu161=)	GPD1L	Single nucleotide variant (synonymous variant)	Brugada syndrome	GLikely benign
Select item 2915025	NM_015141.4(GPD1L):c.618+19dup	GPD1L	Duplication (intron variant)	Brugada syndrome	GBenign
Select item 2911905	NM_015141.4(GPD1L):c.44A>G (p.Asn15Ser)	GPD1L, LOC129936414 (N15S)	Single nucleotide variant (missense variant)	Brugada syndrome	GUncertain significance
Select item 2904884	NM_015141.4(GPD1L):c.382C>T (p.Pro128Ser)	GPD1L (P128S)	Single nucleotide variant (missense variant)	Brugada syndrome	GUncertain significance
Select item 2898686	NM_015141.4(GPD1L):c.960-8C>T	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome	GLikely benign
Select item 2893983	NM_015141.4(GPD1L):c.959+20A>T	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome	GLikely benign
Select item 2893351	NM_015141.4(GPD1L):c.959+15C>T	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome	GLikely benign
Select item 2890366	NM_015141.4(GPD1L):c.852+12C>T	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome	GLikely benign
Select item 2883866	NM_015141.4(GPD1L):c.225+14del	GPD1L	Deletion (intron variant)	Brugada syndrome	GLikely benign
Select item 2873220	NM_015141.4(GPD1L):c.607G>C (p.Gly203Arg)	GPD1L (G203R)	Single nucleotide variant (missense variant)	Brugada syndrome	GUncertain significance
Select item 2856692	NM_015141.4(GPD1L):c.594T>C (p.Thr198=)	GPD1L	Single nucleotide variant (synonymous variant)	Brugada syndrome	GLikely benign
Select item 2841941	NM_015141.4(GPD1L):c.226-4G>T	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome	GLikely benign
Select item 2837793	NM_015141.4(GPD1L):c.47+19G>C	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome	GLikely benign
Select item 2832358	NM_015141.4(GPD1L):c.852+14T>G	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome	GLikely benign
Select item 2809362	NM_015141.4(GPD1L):c.69A>C (p.Ile23=)	GPD1L	Single nucleotide variant (synonymous variant)	Brugada syndrome	GLikely benign
Select item 2795165	NM_015141.4(GPD1L):c.177C>T (p.Asp59=)	GPD1L	Single nucleotide variant (synonymous variant)	Brugada syndrome	GLikely benign
Select item 2777064	NM_015141.4(GPD1L):c.506-9T>C	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome	GLikely benign
Select item 2775481	NM_015141.4(GPD1L):c.288C>G (p.Pro96=)	GPD1L	Single nucleotide variant (synonymous variant)	Brugada syndrome	GLikely benign
Select item 2772133	NM_015141.4(GPD1L):c.451G>A (p.Gly151Arg)	GPD1L (G151R)	Single nucleotide variant (missense variant)	Brugada syndrome	GUncertain significance
Select item 2760734	NM_015141.4(GPD1L):c.565C>T (p.Arg189Ter)	GPD1L (R189*)	Single nucleotide variant (nonsense)	Brugada syndrome	GUncertain significance
Select item 2758056	NM_015141.4(GPD1L):c.1027T>G (p.Cys343Gly)	GPD1L (C343G)	Single nucleotide variant (missense variant)	Brugada syndrome	GUncertain significance
Select item 2739281	NM_015141.4(GPD1L):c.1008A>G (p.Pro336=)	GPD1L	Single nucleotide variant (synonymous variant)	Brugada syndrome	GLikely benign
Select item 2739041	NM_015141.4(GPD1L):c.960-4C>T	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome	GLikely benign
Select item 2737846	NM_015141.4(GPD1L):c.59T>C (p.Val20Ala)	GPD1L (V20A)	Single nucleotide variant (missense variant)	Brugada syndrome	GUncertain significance
Select item 2727541	NM_015141.4(GPD1L):c.225+13G>A	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome	GLikely benign
Select item 2727334	NM_015141.4(GPD1L):c.48-15C>T	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome	GLikely benign
Select item 2722738	NM_015141.4(GPD1L):c.618+8C>T	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome	GLikely benign
Select item 2720729	NM_015141.4(GPD1L):c.960-6A>C	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome	GLikely benign
Select item 2715191	NM_015141.4(GPD1L):c.249G>A (p.Glu83=)	GPD1L	Single nucleotide variant (synonymous variant)	Brugada syndrome	GLikely benign
Select item 2709202	NM_015141.4(GPD1L):c.506-19T>C	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome	GLikely benign
Select item 2662773	NM_015141.4(GPD1L):c.5C>T (p.Ala2Val)	GPD1L, LOC129936414 (A2V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2662442	NM_015141.4(GPD1L):c.842G>A (p.Arg281Lys)	GPD1L (R281K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2626249	NM_015141.4(GPD1L):c.535T>C (p.Phe179Leu)	GPD1L (F179L)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 2626248	NM_015141.4(GPD1L):c.639T>G (p.Ala213=)	GPD1L	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 2564421	NM_015141.4(GPD1L):c.827C>T (p.Ala276Val)	GPD1L (A276V)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 2564420	NM_015141.4(GPD1L):c.861A>G (p.Glu287=)	GPD1L	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 2564419	NM_015141.4(GPD1L):c.936C>G (p.Leu312=)	GPD1L	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 2564418	NM_015141.4(GPD1L):c.454G>A (p.Ala152Thr)	GPD1L (A152T)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 2564417	NM_015141.4(GPD1L):c.528C>A (p.Gly176=)	GPD1L	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 2564416	NM_015141.4(GPD1L):c.911C>T (p.Thr304Ile)	GPD1L (T304I)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 2564415	NM_015141.4(GPD1L):c.740G>A (p.Gly247Asp)	GPD1L (G247D)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 2561882	NM_015141.4(GPD1L):c.48-4G>A	GPD1L	Single nucleotide variant (intron variant)	Cardiovascular phenotype	GLikely benign
Select item 2494261	NM_015141.4(GPD1L):c.746T>C (p.Val249Ala)	GPD1L (V249A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2492364	NM_015141.4(GPD1L):c.116A>G (p.Lys39Arg)	GPD1L (K39R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2482985	NM_015141.4(GPD1L):c.1028G>A (p.Cys343Tyr)	GPD1L (C343Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2449703	NM_015141.4(GPD1L):c.1028G>C (p.Cys343Ser)	GPD1L (C343S)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 2449702	NM_015141.4(GPD1L):c.504C>T (p.Ile168=)	GPD1L	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GConflicting classifications of pathogenicity
Select item 2449700	NM_015141.4(GPD1L):c.967T>C (p.Leu323=)	GPD1L	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 2449699	NM_015141.4(GPD1L):c.611C>G (p.Ala204Gly)	GPD1L (A204G)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 2445719	NM_015141.4(GPD1L):c.47+17T>C	GPD1L	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 2416507	NM_015141.4(GPD1L):c.225+20T>A	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome	GLikely benign
Select item 2280054	NM_015141.4(GPD1L):c.631G>A (p.Val211Met)	GPD1L (V211M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2195796	NM_015141.4(GPD1L):c.1053A>G (p.Thr351=)	GPD1L	Single nucleotide variant (synonymous variant)	Brugada syndrome +1 more	GLikely benign
Select item 2193222	NM_015141.4(GPD1L):c.493G>A (p.Glu165Lys)	GPD1L (E165K)	Single nucleotide variant (missense variant)	Brugada syndrome	GUncertain significance
Select item 2181088	NM_015141.4(GPD1L):c.366+14A>G	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome	GLikely benign
Select item 2176192	NM_015141.4(GPD1L):c.99A>T (p.Lys33Asn)	GPD1L (K33N)	Single nucleotide variant (missense variant)	Brugada syndrome	GUncertain significance
Select item 2173938	NM_015141.4(GPD1L):c.27C>T (p.Cys9=)	GPD1L, LOC129936414	Single nucleotide variant (synonymous variant)	Brugada syndrome	GLikely benign
Select item 2170007	NM_015141.4(GPD1L):c.333G>A (p.Val111=)	GPD1L	Single nucleotide variant (synonymous variant)	Brugada syndrome	GLikely benign
Select item 2169456	NM_015141.4(GPD1L):c.510C>T (p.Ser170=)	GPD1L	Single nucleotide variant (synonymous variant)	Brugada syndrome	GLikely benign
Select item 2168538	NM_015141.4(GPD1L):c.372A>C (p.Ile124=)	GPD1L	Single nucleotide variant (synonymous variant)	Brugada syndrome	GLikely benign
Select item 2161165	NM_015141.4(GPD1L):c.505+8C>G	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome	GLikely benign
Select item 2153693	NM_015141.4(GPD1L):c.216A>T (p.Pro72=)	GPD1L	Single nucleotide variant (synonymous variant)	Brugada syndrome	GLikely benign
Select item 2131931	NM_015141.4(GPD1L):c.226-7G>T	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome	GLikely benign
Select item 2128345	NM_015141.4(GPD1L):c.286C>T (p.Pro96Ser)	GPD1L (P96S)	Single nucleotide variant (missense variant)	Brugada syndrome	GUncertain significance
Select item 2090666	NM_015141.4(GPD1L):c.798C>T (p.Thr266=)	GPD1L	Single nucleotide variant (synonymous variant)	Brugada syndrome	GLikely benign
Select item 2073882	NM_015141.4(GPD1L):c.48-13A>G	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome	GLikely benign
Select item 2063782	NM_015141.4(GPD1L):c.189A>G (p.Val63=)	GPD1L	Single nucleotide variant (synonymous variant)	Brugada syndrome +1 more	GLikely benign
Select item 2037065	NM_015141.4(GPD1L):c.853-15T>A	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome	GLikely benign
Select item 2036617	NM_015141.4(GPD1L):c.696G>A (p.Leu232=)	GPD1L	Single nucleotide variant (synonymous variant)	Brugada syndrome	GLikely benign
Select item 1984232	NM_015141.4(GPD1L):c.763C>G (p.Leu255Val)	GPD1L (L255V)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 1982554	NM_015141.4(GPD1L):c.959+12A>C	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome	GLikely benign
Select item 1975621	NM_015141.4(GPD1L):c.261_262insCTT (p.Asp87_Ala88insLeu)	GPD1L	Insertion (inframe_insertion)	Brugada syndrome	GUncertain significance
Select item 1935316	NM_015141.4(GPD1L):c.960-14T>C	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome	GLikely benign
Select item 1906102	NM_015141.4(GPD1L):c.566G>A (p.Arg189Gln)	GPD1L (R189Q)	Single nucleotide variant (missense variant)	Brugada syndrome	GUncertain significance
Select item 1905154	NM_015141.4(GPD1L):c.625G>A (p.Val209Ile)	GPD1L (V209I)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1903570	NM_015141.4(GPD1L):c.529C>T (p.Leu177Phe)	GPD1L (L177F)	Single nucleotide variant (missense variant)	Brugada syndrome	GUncertain significance
Select item 1878912	NM_015141.4(GPD1L):c.137C>G (p.Thr46Arg)	GPD1L (T46R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1801384	NM_015141.4(GPD1L):c.225+2463_225+2505del	GPD1L	Deletion (intron variant)	Schizophrenia	GUncertain significance
Select item 1798484	NM_015141.4(GPD1L):c.298A>C (p.Ile100Leu)	GPD1L (I100L)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1797786	NM_015141.4(GPD1L):c.292C>G (p.Gln98Glu)	GPD1L (Q98E)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1796690	NM_015141.4(GPD1L):c.283A>G (p.Ile95Val)	GPD1L (I95V)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1790009	NM_015141.4(GPD1L):c.1008A>T (p.Pro336=)	GPD1L	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 1785192	NM_015141.4(GPD1L):c.205C>T (p.His69Tyr)	GPD1L (H69Y)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1779800	NM_015141.4(GPD1L):c.105C>T (p.Ala35=)	GPD1L	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 1776571	NM_015141.4(GPD1L):c.104C>G (p.Ala35Gly)	GPD1L (A35G)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1768720	NM_015141.4(GPD1L):c.995A>C (p.Tyr332Ser)	GPD1L (Y332S)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1766463	NM_015141.4(GPD1L):c.929G>A (p.Arg310His)	GPD1L (R310H)	Single nucleotide variant (missense variant)	Brugada syndrome +1 more	GUncertain significance
Select item 1763917	NM_015141.4(GPD1L):c.857T>C (p.Ile286Thr)	GPD1L (I286T)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1763141	NM_015141.4(GPD1L):c.837C>G (p.Phe279Leu)	GPD1L (F279L)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance

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