MYO1C[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1183863	NM_001080779.2(MYO1C):c.*197C>T	MYO1C	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1276129	NM_001080779.2(MYO1C):c.*109G>A	MYO1C	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1283328	NM_001080779.2(MYO1C):c.3166-32C>T	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1228948	NM_001080779.2(MYO1C):c.3166-44G>A	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 683250	NM_001080779.2(MYO1C):c.3166-87A>G	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1249204	NM_001080779.2(MYO1C):c.3166-292A>G	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1230321	NM_001080779.2(MYO1C):c.3166-320C>T	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1284188	NM_001080779.2(MYO1C):c.3165+281A>G	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1266641	NM_001080779.2(MYO1C):c.3165+77A>G	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 508122	NM_001080779.2(MYO1C):c.3159G>T (p.Leu1053=)	MYO1C	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 513744	NM_001080779.2(MYO1C):c.3150C>T (p.Asn1050=)	MYO1C	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2596852	NM_001080779.2(MYO1C):c.3122C>T (p.Ser1041Leu)	MYO1C (S1022L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1675652	NM_001080779.2(MYO1C):c.3072G>A (p.Thr1024=)	MYO1C	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1254983	NM_001080779.2(MYO1C):c.3065+54G>A	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1316608	NM_001080779.2(MYO1C):c.3065+46_3065+47del	MYO1C	Deletion (intron variant)	not provided	GLikely benign
Select item 682721	NM_001080779.2(MYO1C):c.3065+35G>A	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1316116	NM_001080779.2(MYO1C):c.3065+31C>T	MYO1C	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 682784	NM_001080779.2(MYO1C):c.3065+21G>A	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3163334	NM_001080779.2(MYO1C):c.3060G>C (p.Gln1020His)	MYO1C (Q1020H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461842	NM_001080779.2(MYO1C):c.3037G>A (p.Val1013Met)	MYO1C (V1013M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3297787	NM_001080779.2(MYO1C):c.3005C>T (p.Thr1002Met)	MYO1C (T978M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3045414	NM_001080779.2(MYO1C):c.2994C>T (p.His998=)	MYO1C	Single nucleotide variant (synonymous variant)	MYO1C-related disorder	GLikely benign
Select item 1291838	NM_001080779.2(MYO1C):c.2968-8dup	MYO1C	Duplication (intron variant)	not provided	GBenign
Select item 1273128	NM_001080779.2(MYO1C):c.2968-52G>T	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1240817	NM_001080779.2(MYO1C):c.2967+46A>G	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1247147	NM_001080779.2(MYO1C):c.2967+36T>C	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1293713	NM_001080779.2(MYO1C):c.2967+11A>G	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 781233	NM_001080779.2(MYO1C):c.2940T>C (p.His980=)	MYO1C	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2475522	NM_001080779.2(MYO1C):c.2884G>A (p.Ala962Thr)	MYO1C (A927T +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 508632	NM_001080779.2(MYO1C):c.2856C>T (p.Asp952=)	MYO1C	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 508591	NM_001080779.2(MYO1C):c.2853G>A (p.Glu951=)	MYO1C	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 2604459	NM_001080779.2(MYO1C):c.2842G>A (p.Val948Ile)	MYO1C (V924I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 513840	NM_001080779.2(MYO1C):c.2841C>T (p.Val947=)	MYO1C	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2594536	NM_001080779.2(MYO1C):c.2836G>A (p.Ala946Thr)	MYO1C (A927T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320836	NM_001080779.2(MYO1C):c.2833A>G (p.Asn945Asp)	MYO1C (N945D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 757739	NM_001080779.2(MYO1C):c.2817G>A (p.Gln939=)	MYO1C	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 508143	NM_001080779.2(MYO1C):c.2802G>A (p.Lys934=)	MYO1C	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 2213556	NM_001080779.2(MYO1C):c.2789G>A (p.Arg930His)	MYO1C (R911H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 517826	NM_001080779.2(MYO1C):c.2785G>A (p.Asp929Asn)	MYO1C (D894N +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 2555166	NM_001080779.2(MYO1C):c.2765C>T (p.Ala922Val)	MYO1C (A922V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1275906	NM_001080779.2(MYO1C):c.2761-56G>C	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1321470	NM_001080779.2(MYO1C):c.2760+37G>A	MYO1C	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1316264	NM_001080779.2(MYO1C):c.2760+11G>A	MYO1C	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3163296	NM_001080779.2(MYO1C):c.2735A>G (p.Gln912Arg)	MYO1C (Q893R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214277	NM_001080779.2(MYO1C):c.2726G>A (p.Arg909Gln)	MYO1C (R874Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 508616	NM_001080779.2(MYO1C):c.2649C>A (p.Gly883=)	MYO1C	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3046728	NM_001080779.2(MYO1C):c.2625C>T (p.Ala875=)	MYO1C	Single nucleotide variant (synonymous variant)	MYO1C-related disorder	GLikely benign
Select item 1318162	NM_001080779.2(MYO1C):c.2611-18C>A	MYO1C	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 682653	NM_001080779.2(MYO1C):c.2611-24T>C	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1253586	NM_001080779.2(MYO1C):c.2611-28=	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1228905	NM_001080779.2(MYO1C):c.2611-139G>A	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1261230	NM_001080779.2(MYO1C):c.2611-185G>A	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1244280	NM_001080779.2(MYO1C):c.2611-206C>T	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1230326	NM_001080779.2(MYO1C):c.2611-218=	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1245582	NM_001080779.2(MYO1C):c.2611-245C>G	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1290970	NM_001080779.2(MYO1C):c.2610+189C>T	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1232199	NM_001080779.2(MYO1C):c.2596G>A (p.Glu866Lys)	MYO1C (E831K +3 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 218505	NM_001080779.2(MYO1C):c.2574A>C (p.Lys858Asn)	MYO1C (K858N +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 2476715	NM_001080779.2(MYO1C):c.2542C>T (p.Arg848Trp)	MYO1C (R829W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 682652	NM_001080779.2(MYO1C):c.2527-62C>T	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1239805	NM_001080779.2(MYO1C):c.2527-79A>C	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1274108	NM_001080779.2(MYO1C):c.2527-205C>T	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1278767	NM_001080779.2(MYO1C):c.2526+138_2526+139insA	MYO1C	Insertion (intron variant)	not provided	GBenign
Select item 2317152	NM_001080779.2(MYO1C):c.2488G>C (p.Asp830His)	MYO1C (D795H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 512849	NM_001080779.2(MYO1C):c.2487G>A (p.Leu829=)	MYO1C	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 508101	NM_001080779.2(MYO1C):c.2477A>G (p.Gln826Arg)	MYO1C (Q791R +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 2410145	NM_001080779.2(MYO1C):c.2469G>T (p.Gln823His)	MYO1C (Q804H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 683482	NM_001080779.2(MYO1C):c.2437C>T (p.Arg813Cys)	MYO1C (R813C +3 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2597439	NM_001080779.2(MYO1C):c.2428G>C (p.Asp810His)	MYO1C (D791H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613317	NM_001080779.2(MYO1C):c.2425C>G (p.Leu809Val)	MYO1C (L785V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2647182	NM_001080779.2(MYO1C):c.2415C>T (p.Asn805=)	MYO1C	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2689513	NM_001080779.2(MYO1C):c.2410G>A (p.Glu804Lys)	MYO1C (E769K +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3051574	NM_001080779.2(MYO1C):c.2409C>G (p.Pro803=)	MYO1C	Single nucleotide variant (synonymous variant)	MYO1C-related disorder	GLikely benign
Select item 730875	NM_001080779.2(MYO1C):c.2409C>T (p.Pro803=)	MYO1C	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2215997	NM_001080779.2(MYO1C):c.2401C>T (p.Arg801Cys)	MYO1C (R777C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262074	NM_001080779.2(MYO1C):c.2398C>T (p.Pro800Ser)	MYO1C (P765S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1293745	NM_001080779.2(MYO1C):c.2395G>A (p.Ala799Thr)	MYO1C (A764T +3 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2324744	NM_001080779.2(MYO1C):c.2394C>A (p.His798Gln)	MYO1C (H774Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1317782	NM_001080779.2(MYO1C):c.2385C>T (p.Val795=)	MYO1C	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 508100	NM_001080779.2(MYO1C):c.2383G>A (p.Val795Ile)	MYO1C (V760I +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 508613	NM_001080779.2(MYO1C):c.2367-8C>A	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1316605	NM_001080779.2(MYO1C):c.2366+36A>G	MYO1C	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1317762	NM_001080779.2(MYO1C):c.2366+20G>A	MYO1C	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3297790	NM_001080779.2(MYO1C):c.2359A>C (p.Ile787Leu)	MYO1C (I763L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320174	NM_001080779.2(MYO1C):c.2357C>A (p.Thr786Asn)	MYO1C (T767N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 516881	NM_001080779.2(MYO1C):c.2353C>A (p.Gln785Lys)	MYO1C (Q750K +3 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2350711	NM_001080779.2(MYO1C):c.2336A>G (p.Lys779Arg)	MYO1C (K744R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1266833	NM_001080779.2(MYO1C):c.2281+47G>A	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2329490	NM_001080779.2(MYO1C):c.2273A>T (p.Lys758Met)	MYO1C (K734M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3238919	NM_001080779.2(MYO1C):c.2252G>A (p.Arg751Gln)	MYO1C (R716Q +3 more)	Single nucleotide variant (missense variant)	Meniere disease	GUncertain significance
Select item 1317788	NM_001080779.2(MYO1C):c.2251C>T (p.Arg751Trp)	MYO1C (R716W +3 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1326181	NM_001080779.2(MYO1C):c.2213-62G>A	MYO1C	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1263102	NM_001080779.2(MYO1C):c.2212+170C>T	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2308405	NM_001080779.2(MYO1C):c.2209C>G (p.Leu737Val)	MYO1C (L702V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543968	NM_001080779.2(MYO1C):c.2201G>A (p.Arg734Gln)	MYO1C (R699Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346451	NM_001080779.2(MYO1C):c.2180A>G (p.Glu727Gly)	MYO1C (E692G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3041503	NM_001080779.2(MYO1C):c.2136-10G>A	MYO1C	Single nucleotide variant (intron variant)	MYO1C-related disorder	GLikely benign
Select item 1290739	NM_001080779.2(MYO1C):c.2135+18C>T	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 682794	NM_001080779.2(MYO1C):c.2135+14G>A	MYO1C	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3297784	NM_001080779.2(MYO1C):c.2086G>T (p.Val696Leu)	MYO1C (V661L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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