MYOCD[gene] - ClinVar

Search results

Items: 97

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 154089	GRCh38/hg38 17p13.3-12(chr17:150732-14764202)x3	LOC130060143, LOC130060144 +963 more	Copy number gain	See cases	GPathogenic
Select item 58693	GRCh38/hg38 17p12-11.2(chr17:10892259-17964282)x3	LOC130060335, LOC130060336 +242 more	Copy number gain	See cases	GPathogenic
Select item 1707454	Single allele	ADORA2B, ARHGAP44 +228 more	Duplication	not specified	GPathogenic
Select item 689482	NC_000017.11:g.12269251_12706280del	LINC00670, LOC125177420 +5 more	Deletion	Megabladder, congenital +1 more	GPathogenic
Select item 1289485	NC_000017.11:g.12665560A>T	MYOCD	Single nucleotide variant	not provided	GBenign
Select item 1253022	NC_000017.11:g.12665754T>C	MYOCD	Single nucleotide variant	not provided	GBenign
Select item 1222452	NM_001146312.3(MYOCD):c.-64G>A	MYOCD	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 1182207	NM_001146312.3(MYOCD):c.56-174T>C	MYOCD, MYOCD-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2235702	NM_001146312.3(MYOCD):c.109G>C (p.Gly37Arg)	MYOCD, MYOCD-AS1 (G37R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1222172	NM_001146312.3(MYOCD):c.122-209_122-208insCT	MYOCD	Insertion (intron variant)	not provided	GBenign
Select item 1265097	NM_001146312.3(MYOCD):c.122-156G>C	MYOCD	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 768833	NM_001146312.3(MYOCD):c.226G>A (p.Asp76Asn)	MYOCD (D76N)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1225489	NM_001146312.3(MYOCD):c.253+23A>G	MYOCD	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1229503	NM_001146312.3(MYOCD):c.253+159G>A	MYOCD	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1245866	NM_001146312.3(MYOCD):c.254-238G>A	MYOCD	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 689480	NM_001146312.3(MYOCD):c.343C>T (p.Arg115Ter)	MYOCD (R115* +1 more)	Single nucleotide variant (nonsense)	Megabladder, congenital +1 more	GPathogenic
Select item 2554680	NM_001146312.3(MYOCD):c.358G>A (p.Glu120Lys)	MYOCD (E120K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2318396	NM_001146312.3(MYOCD):c.359A>G (p.Glu120Gly)	MYOCD (E120G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1220717	NM_001146312.3(MYOCD):c.416-184T>C	MYOCD	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 779171	NM_001146312.3(MYOCD):c.423G>A (p.Gln141=)	MYOCD	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1301582	NM_001146312.3(MYOCD):c.506G>A (p.Ser169Asn)	MYOCD (S169N +1 more)	Single nucleotide variant (missense variant)	Megabladder, congenital +1 more	GConflicting classifications of pathogenicity
Select item 100828	NM_001146312.3(MYOCD):c.543C>T (p.Asp181=)	MYOCD	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 1262861	NM_001146312.3(MYOCD):c.592-253TA[5]	MYOCD	Microsatellite (intron variant)	not provided	GBenign
Select item 2593820	NM_001146312.3(MYOCD):c.659C>T (p.Ala220Val)	MYOCD (A220V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 689495	NM_001146312.3(MYOCD):c.684dup (p.Ser229fs)	MYOCD (S229fs +1 more)	Duplication (frameshift variant)	Not Specified	Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant
Select item 689479	NM_001146312.2(MYOCD):c.[1589A>G;684dup]	MYOCD (S229fs +3 more)	Duplication (frameshift variant +1 more)	Prune belly syndrome	GPathogenic
Select item 1264358	NM_001146312.3(MYOCD):c.717+245T>C	MYOCD	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1221524	NM_001146312.3(MYOCD):c.718-92A>G	MYOCD	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1181987	NM_001146312.3(MYOCD):c.718-10T>C	MYOCD	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2345161	NM_001146312.3(MYOCD):c.935G>A (p.Arg312Gln)	MYOCD (R233Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1328432	NM_001146312.3(MYOCD):c.971+3_971+6del	MYOCD	Microsatellite (splice donor variant)	Megabladder, congenital	GLikely pathogenic
Select item 1287815	NM_001146312.3(MYOCD):c.971+235T>C	MYOCD	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2617828	NM_001146312.3(MYOCD):c.991G>C (p.Val331Leu)	MYOCD (V252L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 689481	NM_001146312.3(MYOCD):c.1053_1054del (p.Asn351fs)	MYOCD (N351fs +1 more)	Deletion (frameshift variant)	Megabladder, congenital +1 more	GPathogenic
Select item 1231799	NM_001146312.3(MYOCD):c.1125+271G>A	MYOCD	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2499887	NM_001146312.3(MYOCD):c.1208C>T (p.Pro403Leu)	MYOCD (P324L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 183354	NM_001146312.3(MYOCD):c.1252A>G (p.Ile418Val)	MYOCD (I418V +1 more)	Single nucleotide variant (missense variant)	not specified	GBenign
Select item 2390197	NM_001146312.3(MYOCD):c.1256C>T (p.Thr419Met)	MYOCD (T340M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2609816	NM_001146312.3(MYOCD):c.1415C>G (p.Pro472Arg)	MYOCD (P393R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2479065	NM_001146312.3(MYOCD):c.1439C>A (p.Pro480His)	MYOCD (P480H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 707960	NM_001146312.3(MYOCD):c.1447G>A (p.Gly483Ser)	MYOCD (G483S +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2310183	NM_001146312.3(MYOCD):c.1493T>C (p.Met498Thr)	MYOCD (M419T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1235452	NM_001146312.3(MYOCD):c.1506T>C (p.Asn502=)	MYOCD	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 689496	NM_001146312.3(MYOCD):c.1589A>G (p.Glu530Gly)	MYOCD (E530G +1 more)	Single nucleotide variant (missense variant)	Not Specified	Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant
Select item 3025973	NM_001146312.3(MYOCD):c.1628A>G (p.Glu543Gly)	MYOCD (E464G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2552373	NM_001146312.3(MYOCD):c.1685C>T (p.Pro562Leu)	MYOCD (P483L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2377918	NM_001146312.3(MYOCD):c.1734C>A (p.Ser578Arg)	MYOCD (S578R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2377919	NM_001146312.3(MYOCD):c.1735T>G (p.Cys579Gly)	MYOCD (C500G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2224397	NM_001146312.3(MYOCD):c.1748C>T (p.Ser583Phe)	MYOCD (S504F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2361103	NM_001146312.3(MYOCD):c.1801T>C (p.Cys601Arg)	MYOCD (C522R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1281605	NM_001146312.3(MYOCD):c.1812T>C (p.Ala604=)	MYOCD	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2610583	NM_001146312.3(MYOCD):c.1843G>A (p.Val615Met)	MYOCD (V536M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2647492	NM_001146312.3(MYOCD):c.1885C>A (p.Leu629Ile)	MYOCD (L550I +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 713293	NM_001146312.3(MYOCD):c.1917G>A (p.Pro639=)	MYOCD	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1257154	NM_001146312.3(MYOCD):c.1941G>C (p.Gln647His)	MYOCD (Q568H +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2464609	NM_001146312.3(MYOCD):c.1952T>G (p.Leu651Trp)	MYOCD (L651W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2411041	NM_001146312.3(MYOCD):c.1966A>C (p.Asn656His)	MYOCD (N577H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2531993	NM_001146312.3(MYOCD):c.2000C>T (p.Ala667Val)	MYOCD (A588V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1225965	NM_001146312.3(MYOCD):c.2058+48G>A	MYOCD	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1265493	NM_001146312.3(MYOCD):c.2058+151C>A	MYOCD	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1263840	NM_001146312.3(MYOCD):c.2058+152C>T	MYOCD	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1267010	NM_001146312.3(MYOCD):c.2059-232C>T	MYOCD	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2319687	NM_001146312.3(MYOCD):c.2073C>A (p.His691Gln)	MYOCD (H691Q +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2647493	NM_001146312.3(MYOCD):c.2074G>A (p.Asp692Asn)	MYOCD (D613N +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2314512	NM_001146312.3(MYOCD):c.2078G>C (p.Gly693Ala)	MYOCD (G693A +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2208243	NM_001146312.3(MYOCD):c.2102A>G (p.His701Arg)	MYOCD (H622R +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 786432	NM_001146312.3(MYOCD):c.2118C>T (p.His706=)	MYOCD	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2216155	NM_001146312.3(MYOCD):c.2185C>G (p.Pro729Ala)	MYOCD (P650A +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1265297	NM_001146312.3(MYOCD):c.2202+232G>A	MYOCD	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2647494	NM_001146312.3(MYOCD):c.2225A>G (p.Asp742Gly)	MYOCD (D663G +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1272626	NM_001146312.3(MYOCD):c.2332-271G>A	ARHGAP44-AS1, MYOCD	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1277125	NM_001146312.3(MYOCD):c.2332-246G>T	ARHGAP44-AS1, MYOCD	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1268409	NM_001146312.3(MYOCD):c.2332-126C>T	ARHGAP44-AS1, MYOCD	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2270670	NM_001146312.3(MYOCD):c.2342G>A (p.Arg781Gln)	ARHGAP44-AS1, MYOCD (R702Q +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1279478	NM_001146312.3(MYOCD):c.2389+153T>C	ARHGAP44-AS1, MYOCD	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1269164	NM_001146312.3(MYOCD):c.2389+297_2389+300del	ARHGAP44-AS1, MYOCD	Microsatellite (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2335826	NM_001146312.3(MYOCD):c.2404G>A (p.Ala802Thr)	MYOCD, ARHGAP44-AS1 (A802T +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2321719	NM_001146312.3(MYOCD):c.2408G>A (p.Arg803Lys)	MYOCD, ARHGAP44-AS1 (R724K +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2647495	NM_001146312.3(MYOCD):c.2520C>A (p.Ser840Arg)	ARHGAP44-AS1, MYOCD (S761R +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2560241	NM_001146312.3(MYOCD):c.2536C>T (p.Pro846Ser)	ARHGAP44-AS1, MYOCD (P846S +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2270163	NM_001146312.3(MYOCD):c.2634C>A (p.Ser878Arg)	MYOCD, ARHGAP44-AS1 (S799R +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 780416	NM_001146312.3(MYOCD):c.2634C>T (p.Ser878=)	ARHGAP44-AS1, MYOCD	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 161824	NM_001146312.3(MYOCD):c.2678del (p.Lys893fs)	ARHGAP44-AS1, MYOCD (K845fs +2 more)	Deletion (non-coding transcript variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 2393418	NM_001146312.3(MYOCD):c.2689G>C (p.Asp897His)	ARHGAP44-AS1, MYOCD (D849H +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +1 more	GUncertain significance
Select item 780417	NM_001146312.3(MYOCD):c.2721C>G (p.Gly907=)	ARHGAP44-AS1, MYOCD	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2479258	NM_001146312.3(MYOCD):c.2737C>A (p.Gln913Lys)	ARHGAP44-AS1, MYOCD (Q834K +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 780418	NM_001146312.3(MYOCD):c.2739G>A (p.Gln913=)	ARHGAP44-AS1, MYOCD	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2459173	NM_001146312.3(MYOCD):c.2792C>G (p.Thr931Ser)	ARHGAP44-AS1, MYOCD (T852S +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2354480	NM_001146312.3(MYOCD):c.2834C>T (p.Pro945Leu)	MYOCD, ARHGAP44-AS1 (P897L +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2381886	NM_001146312.3(MYOCD):c.2893A>G (p.Ile965Val)	ARHGAP44-AS1, MYOCD (I917V +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3063486	GRCh37/hg19 17p13.3-11.2(chr17:525-21510992)x3	ABR, ACADVL +329 more	Copy number gain	not specified	GPathogenic
Select item 1339912	GRCh37/hg19 17p12-11.2(chr17:12524223-16047567)x1	ADORA2B, ARHGAP44 +18 more	Copy number loss	Hereditary liability to pressure palsies	Gnot provided
Select item 929830	GRCh37/hg19 17p13.1-12(chr17:10493837-15099023)x1	ADPRM, ARHGAP44 +14 more	Copy number loss	See cases	GUncertain significance
Select item 443659	GRCh37/hg19 17p13.3-12(chr17:525-15027737)x3	ABR, ACADVL +250 more	Copy number gain	See cases	GPathogenic
Select item 441816	GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3	TNFSF12, TNFSF12-TNFSF13 +1143 more	Copy number gain	See cases	GPathogenic
Select item 441815	GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)	AIPL1, AKAP1 +1143 more	Copy number gain	See cases	GPathogenic
Select item 221346	Single allele	ADORA2B, ADPRM +41 more	Complex	Breast ductal adenocarcinoma	GUncertain significance

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Items: 97