ClinVar for Gene (Select 4650) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3065363	NM_004145.4(MYO9B):c.6016G>A (p.Glu2006Lys)	MYO9B (E2006K)	Single nucleotide variant (missense variant)	Celiac disease, susceptibility to, 4	GUncertain significance
Select item 3062393	GRCh37/hg19 19p13.13-13.11(chr19:13970692-18139376)x3	CYP4F8, DCAF15 +109 more	Copy number gain	not specified	GUncertain significance
Select item 3062387	GRCh37/hg19 19p13.11(chr19:16857649-17423590)x3	NR2F6, NWD1 +13 more	Copy number gain	not specified	GUncertain significance
Select item 3059054	NM_004145.4(MYO9B):c.5589G>A (p.Pro1863=)	MYO9B	Single nucleotide variant (synonymous variant)	MYO9B-related condition	GBenign
Select item 3057127	NM_004145.4(MYO9B):c.44C>T (p.Ala15Val)	MYO9B (A15V)	Single nucleotide variant (missense variant)	MYO9B-related condition	GLikely benign
Select item 3056992	NM_004145.4(MYO9B):c.2718G>A (p.Leu906=)	MYO9B	Single nucleotide variant (synonymous variant)	MYO9B-related condition	GBenign
Select item 3056521	NM_004145.4(MYO9B):c.243C>T (p.Asn81=)	MYO9B	Single nucleotide variant (synonymous variant)	MYO9B-related condition	GLikely benign
Select item 3055101	NM_004145.4(MYO9B):c.6124G>A (p.Ala2042Thr)	MYO9B (A2042T)	Single nucleotide variant (3 prime UTR variant +1 more)	MYO9B-related condition	GLikely benign
Select item 3053760	NM_004145.4(MYO9B):c.1845T>C (p.His615=)	MYO9B	Single nucleotide variant (synonymous variant)	MYO9B-related condition	GLikely benign
Select item 3053412	NM_004145.4(MYO9B):c.6097A>G (p.Thr2033Ala)	MYO9B (T2033A)	Single nucleotide variant (3 prime UTR variant +1 more)	MYO9B-related condition	GLikely benign
Select item 3051749	NM_004145.4(MYO9B):c.4332C>T (p.His1444=)	MYO9B	Single nucleotide variant (synonymous variant)	MYO9B-related condition	GLikely benign
Select item 3051665	NM_004145.4(MYO9B):c.2382G>A (p.Leu794=)	MYO9B	Single nucleotide variant (synonymous variant)	MYO9B-related condition	GLikely benign
Select item 3050451	NM_004145.4(MYO9B):c.5247G>A (p.Ala1749=)	MYO9B	Single nucleotide variant (synonymous variant)	MYO9B-related condition	GLikely benign
Select item 3049880	NM_004145.4(MYO9B):c.1908C>T (p.Phe636=)	MYO9B	Single nucleotide variant (synonymous variant)	MYO9B-related condition	GBenign
Select item 3049854	NM_004145.4(MYO9B):c.6339G>A (p.Thr2113=)	MYO9B	Single nucleotide variant (3 prime UTR variant +1 more)	MYO9B-related condition	GLikely benign
Select item 3049287	NM_004145.4(MYO9B):c.2292C>G (p.Leu764=)	MYO9B	Single nucleotide variant (synonymous variant)	MYO9B-related condition	GLikely benign
Select item 3049209	NM_004145.4(MYO9B):c.3443G>A (p.Arg1148His)	MYO9B (R1148H)	Single nucleotide variant (missense variant)	MYO9B-related condition	GLikely benign
Select item 3049195	NM_004145.4(MYO9B):c.5400G>A (p.Lys1800=)	MYO9B	Single nucleotide variant (synonymous variant)	MYO9B-related condition	GLikely benign
Select item 3048979	NM_004145.4(MYO9B):c.5260C>G (p.Pro1754Ala)	MYO9B (P1754A)	Single nucleotide variant (missense variant)	MYO9B-related condition	GLikely benign
Select item 3048969	NM_004145.4(MYO9B):c.2127C>T (p.Ala709=)	MYO9B	Single nucleotide variant (synonymous variant)	MYO9B-related condition	GLikely benign
Select item 3048194	NM_004145.4(MYO9B):c.2751C>T (p.Ile917=)	MYO9B	Single nucleotide variant (synonymous variant)	MYO9B-related condition	GBenign
Select item 3048095	NM_004145.4(MYO9B):c.5019C>T (p.Cys1673=)	MYO9B	Single nucleotide variant (synonymous variant)	MYO9B-related condition	GLikely benign
Select item 3046425	NM_004145.4(MYO9B):c.4077C>T (p.Asp1359=)	MYO9B	Single nucleotide variant (synonymous variant)	MYO9B-related condition	GLikely benign
Select item 3046353	NM_004145.4(MYO9B):c.5386+10A>G	MYO9B	Single nucleotide variant (intron variant)	MYO9B-related condition	GLikely benign
Select item 3046179	NM_004145.4(MYO9B):c.2141-5G>A	MYO9B	Single nucleotide variant (intron variant)	MYO9B-related condition	GLikely benign
Select item 3043873	NM_004145.4(MYO9B):c.5258-9A>C	MYO9B	Single nucleotide variant (intron variant)	MYO9B-related condition	GBenign
Select item 3043729	NM_004145.4(MYO9B):c.5622C>T (p.Thr1874=)	MYO9B	Single nucleotide variant (synonymous variant)	MYO9B-related condition	GLikely benign
Select item 3043424	NM_004145.4(MYO9B):c.2958C>T (p.Ile986=)	MYO9B	Single nucleotide variant (synonymous variant)	MYO9B-related condition	GLikely benign
Select item 3042996	NM_004145.4(MYO9B):c.4217C>T (p.Pro1406Leu)	MYO9B (P1406L)	Single nucleotide variant (missense variant)	MYO9B-related condition	GLikely benign
Select item 3042226	NM_004145.4(MYO9B):c.5901T>C (p.Ile1967=)	MYO9B	Single nucleotide variant (synonymous variant)	MYO9B-related condition	GLikely benign
Select item 3042077	NM_004145.4(MYO9B):c.3838G>A (p.Gly1280Ser)	MYO9B (G1280S)	Single nucleotide variant (missense variant)	MYO9B-related condition	GBenign
Select item 3040764	NM_004145.4(MYO9B):c.1287C>T (p.Val429=)	MYO9B	Single nucleotide variant (synonymous variant)	MYO9B-related condition	GLikely benign
Select item 3038958	NM_004145.4(MYO9B):c.5190C>T (p.Thr1730=)	MYO9B	Single nucleotide variant (synonymous variant)	MYO9B-related condition	GLikely benign
Select item 3038330	NM_004145.4(MYO9B):c.3371A>G (p.Glu1124Gly)	MYO9B (E1124G)	Single nucleotide variant (missense variant)	MYO9B-related condition	GBenign
Select item 3037565	NM_004145.4(MYO9B):c.5286C>T (p.Phe1762=)	MYO9B	Single nucleotide variant (synonymous variant)	MYO9B-related condition	GLikely benign
Select item 3037288	NM_004145.4(MYO9B):c.462C>T (p.Leu154=)	MYO9B	Single nucleotide variant (synonymous variant)	MYO9B-related condition	GBenign
Select item 3036971	NM_004145.4(MYO9B):c.5955G>A (p.Pro1985=)	MYO9B	Single nucleotide variant (synonymous variant)	MYO9B-related condition	GLikely benign
Select item 3033989	NM_004145.4(MYO9B):c.4662+6T>G	MYO9B	Single nucleotide variant (intron variant)	MYO9B-related condition	GLikely benign
Select item 3033660	NM_004145.4(MYO9B):c.6284G>A (p.Arg2095Gln)	MYO9B (R2095Q)	Single nucleotide variant (3 prime UTR variant +1 more)	MYO9B-related condition	GBenign
Select item 3033338	NM_004145.4(MYO9B):c.1420-4A>G	MYO9B	Single nucleotide variant (intron variant)	MYO9B-related condition	GLikely benign
Select item 2684887	GRCh37/hg19 19p13.12-13.11(chr19:14888106-17360864)x3	ADGRE2, AKAP8 +55 more	Copy number gain	not provided	GUncertain significance
Select item 2649536	NM_004145.4(MYO9B):c.6456G>A (p.Ser2152=)	MYO9B	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2649535	NM_004145.4(MYO9B):c.6423G>A (p.Ser2141=)	MYO9B	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2649534	NM_004145.4(MYO9B):c.2136T>C (p.Ala712=)	MYO9B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2649533	NM_004145.4(MYO9B):c.2058C>T (p.Ala686=)	MYO9B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2649532	NM_004145.4(MYO9B):c.804C>T (p.Val268=)	MYO9B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2649531	NM_004145.4(MYO9B):c.381G>A (p.Ala127=)	MYO9B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2614629	NM_004145.4(MYO9B):c.4378T>A (p.Ser1460Thr)	MYO9B (S1460T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2608676	NM_004145.4(MYO9B):c.625G>A (p.Gly209Ser)	MYO9B (G209S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2607175	NM_004145.4(MYO9B):c.85G>A (p.Glu29Lys)	MYO9B (E29K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2598580	NM_004145.4(MYO9B):c.4015C>T (p.Arg1339Trp)	MYO9B (R1339W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2597891	NM_004145.4(MYO9B):c.691G>A (p.Val231Met)	MYO9B (V231M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2597780	NM_004145.4(MYO9B):c.5573C>T (p.Pro1858Leu)	MYO9B (P1858L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2596964	NM_004145.4(MYO9B):c.5447A>G (p.Glu1816Gly)	MYO9B (E1816G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2592263	NM_004145.4(MYO9B):c.5231G>A (p.Arg1744Gln)	MYO9B (R1744Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2589015	NM_004145.4(MYO9B):c.6301G>C (p.Ala2101Pro)	MYO9B (A2101P)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2569959	NM_004145.4(MYO9B):c.3064C>T (p.Arg1022Trp)	MYO9B (R1022W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2569125	NM_004145.4(MYO9B):c.4414C>T (p.Arg1472Cys)	MYO9B (R1472C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2568993	NM_004145.4(MYO9B):c.6146C>T (p.Ser2049Leu)	MYO9B (S2049L)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2568955	NM_004145.4(MYO9B):c.3065G>A (p.Arg1022Gln)	MYO9B (R1022Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2552318	NM_004145.4(MYO9B):c.3284G>A (p.Gly1095Glu)	MYO9B (G1095E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2552103	NM_004145.4(MYO9B):c.2134G>A (p.Ala712Thr)	MYO9B (A712T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2546083	NM_004145.4(MYO9B):c.2942G>A (p.Arg981Gln)	MYO9B (R981Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2543496	NM_004145.4(MYO9B):c.1498G>T (p.Ala500Ser)	MYO9B (A500S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2533473	NM_004145.4(MYO9B):c.2078G>A (p.Arg693Gln)	MYO9B (R693Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2529430	NM_004145.4(MYO9B):c.2044G>A (p.Val682Met)	MYO9B (V682M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2526112	NM_004145.4(MYO9B):c.4741G>T (p.Gly1581Cys)	MYO9B (G1581C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2519123	NM_004145.4(MYO9B):c.4729G>A (p.Ala1577Thr)	MYO9B (A1577T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2517874	NM_004145.4(MYO9B):c.3107G>A (p.Arg1036Gln)	MYO9B (R1036Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2514680	NM_004145.4(MYO9B):c.6277C>T (p.Pro2093Ser)	MYO9B (P2093S)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2494355	NM_004145.4(MYO9B):c.5597G>A (p.Ser1866Asn)	MYO9B (S1866N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2489280	NM_004145.4(MYO9B):c.816C>G (p.Ile272Met)	MYO9B (I272M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2485568	NM_004145.4(MYO9B):c.2993C>T (p.Ala998Val)	MYO9B (A998V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2482703	NM_004145.4(MYO9B):c.6002C>T (p.Thr2001Met)	MYO9B (T2001M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2471966	NM_004145.4(MYO9B):c.1739A>G (p.His580Arg)	MYO9B (H580R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2464873	NM_004145.4(MYO9B):c.1184C>A (p.Pro395His)	MYO9B (P395H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2462219	NM_004145.4(MYO9B):c.6328G>A (p.Val2110Met)	MYO9B (V2110M)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2458091	NM_004145.4(MYO9B):c.3146C>T (p.Ser1049Leu)	MYO9B (S1049L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2456450	NM_004145.4(MYO9B):c.437C>T (p.Ala146Val)	MYO9B (A146V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2455862	NM_004145.4(MYO9B):c.5356G>C (p.Ala1786Pro)	MYO9B (A1786P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2425869	NC_000019.9:g.(?_14847048)_(17394124_?)del	ADGRE2, AKAP8 +57 more	Deletion	not provided	GUncertain significance
Select item 2407997	NM_004145.4(MYO9B):c.6290G>A (p.Arg2097Gln)	MYO9B (R2097Q)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2401154	NM_004145.4(MYO9B):c.6094C>T (p.Pro2032Ser)	MYO9B (P2032S)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2401110	NM_004145.4(MYO9B):c.2860C>T (p.Arg954Trp)	MYO9B (R954W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2399987	NM_004145.4(MYO9B):c.4331A>G (p.His1444Arg)	MYO9B (H1444R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2386965	NM_004145.4(MYO9B):c.5095G>A (p.Gly1699Ser)	MYO9B (G1699S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2386283	NM_004145.4(MYO9B):c.3516G>T (p.Glu1172Asp)	MYO9B (E1172D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2385145	NM_004145.4(MYO9B):c.3896G>A (p.Arg1299Gln)	MYO9B (R1299Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2379428	NM_004145.4(MYO9B):c.3433C>T (p.Arg1145Trp)	MYO9B (R1145W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2377948	NM_004145.4(MYO9B):c.2180T>G (p.Leu727Arg)	MYO9B (L727R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2375036	NM_004145.4(MYO9B):c.3214G>A (p.Gly1072Ser)	MYO9B (G1072S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2374669	NM_004145.4(MYO9B):c.3053G>A (p.Arg1018Gln)	MYO9B (R1018Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2374087	NM_004145.4(MYO9B):c.5051C>A (p.Thr1684Asn)	MYO9B (T1684N)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 2372259	NM_004145.4(MYO9B):c.5947C>T (p.Arg1983Trp)	MYO9B (R1983W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2370760	NM_004145.4(MYO9B):c.4470G>T (p.Lys1490Asn)	MYO9B (K1490N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2367230	NM_004145.4(MYO9B):c.4037C>T (p.Thr1346Met)	MYO9B (T1346M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2366741	NM_004145.4(MYO9B):c.3925G>A (p.Ala1309Thr)	MYO9B (A1309T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2365603	NM_004145.4(MYO9B):c.5774C>T (p.Ser1925Leu)	MYO9B (S1925L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2364887	NM_004145.4(MYO9B):c.4142G>A (p.Arg1381Gln)	MYO9B (R1381Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2364476	NM_004145.4(MYO9B):c.5869G>A (p.Gly1957Ser)	MYO9B (G1957S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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