FHOD3[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1294080	NC_000018.10:g.36297479C>G	FHOD3	Single nucleotide variant	not provided	GBenign
Select item 1238474	NC_000018.10:g.36297533G>C	FHOD3	Single nucleotide variant	not provided	GBenign
Select item 1248150	NC_000018.10:g.36297547C>T	FHOD3	Single nucleotide variant	not provided	GBenign
Select item 1243850	NC_000018.10:g.36297703C>G	FHOD3	Single nucleotide variant	not provided	GBenign
Select item 1221085	NM_001281740.3(FHOD3):c.-112T>C	FHOD3	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 1287000	NM_001281740.3(FHOD3):c.-86G>T	FHOD3	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 2284700	NM_001281740.3(FHOD3):c.122C>T (p.Thr41Ile)	FHOD3 (T41I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1233999	NM_001281740.3(FHOD3):c.165+120C>T	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1293316	NM_001281740.3(FHOD3):c.166-200A>G	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1708103	NM_001281740.3(FHOD3):c.172G>C (p.Asp58His)	FHOD3 (D58H)	Single nucleotide variant (missense variant)	Cardiomyopathy, familial hypertrophic, 28	GUncertain significance
Select item 3067377	NM_001281740.3(FHOD3):c.197A>G (p.Asn66Ser)	FHOD3 (N66S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3095136	NM_001281740.3(FHOD3):c.202G>A (p.Ala68Thr)	FHOD3 (A68T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2630984	NM_001281740.3(FHOD3):c.235C>T (p.Gln79Ter)	FHOD3 (Q79*)	Single nucleotide variant (nonsense)	FHOD3-related disorder	GUncertain significance
Select item 1299872	NM_001281740.3(FHOD3):c.238C>T (p.Arg80Trp)	FHOD3 (R80W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2460355	NM_001281740.3(FHOD3):c.239G>A (p.Arg80Gln)	FHOD3 (R80Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1317403	NM_001281740.3(FHOD3):c.272+91A>G	FHOD3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1291039	NM_001281740.3(FHOD3):c.272+205G>C	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3032863	NM_001281740.3(FHOD3):c.336C>A (p.Ile112=)	FHOD3	Single nucleotide variant (synonymous variant)	FHOD3-related disorder	GLikely benign
Select item 1290953	NM_001281740.3(FHOD3):c.338-46A>G	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1291188	NM_001281740.3(FHOD3):c.405+255dup	FHOD3	Duplication (intron variant)	not provided	GBenign
Select item 1246300	NM_001281740.3(FHOD3):c.405+255del	FHOD3	Deletion (intron variant)	not provided	GBenign
Select item 1291985	NM_001281740.3(FHOD3):c.405+287_405+288del	FHOD3	Deletion (intron variant)	not provided	GBenign
Select item 1223337	NM_001281740.3(FHOD3):c.405+298G>A	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1291374	NM_001281740.3(FHOD3):c.406-74G>C	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2247911	NM_001281740.3(FHOD3):c.410A>G (p.Asp137Gly)	FHOD3 (D137G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1258310	NM_001281740.3(FHOD3):c.511+129T>A	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1239915	NM_001281740.3(FHOD3):c.511+148del	FHOD3	Deletion (intron variant)	not provided	GBenign
Select item 1297327	NM_001281740.3(FHOD3):c.511+151_511+158del	FHOD3	Deletion (intron variant)	not provided	GBenign
Select item 1263041	NM_001281740.3(FHOD3):c.512-137C>T	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1228844	NM_001281740.3(FHOD3):c.512-136T>G	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2255423	NM_001281740.3(FHOD3):c.557T>C (p.Ile186Thr)	FHOD3 (I186T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1298257	NM_001281740.3(FHOD3):c.595A>G (p.Ile199Val)	FHOD3 (I199V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1297519	NM_001281740.3(FHOD3):c.606+8del	FHOD3	Deletion (intron variant)	not provided	GLikely benign
Select item 1263609	NM_001281740.3(FHOD3):c.606+241C>T	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1175674	NM_001281740.3(FHOD3):c.607-313C>T	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2571010	NM_001281740.3(FHOD3):c.663G>A (p.Ser221=)	FHOD3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2648676	NM_001281740.3(FHOD3):c.673G>A (p.Ala225Thr)	FHOD3 (A225T)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1271308	NM_001281740.3(FHOD3):c.718+97T>C	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2629302	NM_001281740.3(FHOD3):c.739A>G (p.Ile247Val)	FHOD3 (I247V)	Single nucleotide variant (missense variant)	FHOD3-related disorder	GUncertain significance
Select item 3095157	NM_001281740.3(FHOD3):c.803T>C (p.Leu268Ser)	FHOD3 (L268S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1236733	NM_001281740.3(FHOD3):c.813+69A>G	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1253432	NM_001281740.3(FHOD3):c.813+103G>A	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1294169	NM_001281740.3(FHOD3):c.813+207A>G	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 721884	NM_001281740.3(FHOD3):c.814-6T>C	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3095158	NM_001281740.3(FHOD3):c.826C>A (p.Leu276Ile)	FHOD3 (L276I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095159	NM_001281740.3(FHOD3):c.850G>A (p.Asp284Asn)	FHOD3 (D284N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095160	NM_001281740.3(FHOD3):c.856G>A (p.Val286Met)	FHOD3 (V286M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2367398	NM_001281740.3(FHOD3):c.877G>A (p.Gly293Ser)	FHOD3 (G293S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 713615	NM_001281740.3(FHOD3):c.918G>A (p.Gly306=)	FHOD3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2665093	NM_001281740.3(FHOD3):c.928G>A (p.Asp310Asn)	FHOD3 (D310N)	Single nucleotide variant (missense variant)	Cardiomyopathy, familial hypertrophic, 28	GUncertain significance
Select item 1706765	NM_001281740.3(FHOD3):c.957+29C>G	FHOD3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1259733	NM_001281740.3(FHOD3):c.957+86A>C	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1237951	NM_001281740.3(FHOD3):c.957+102C>T	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1234434	NM_001281740.3(FHOD3):c.958-229G>A	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1228778	NM_001281740.3(FHOD3):c.958-206T>C	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1264697	NM_001281740.3(FHOD3):c.958-178G>A	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1266489	NM_001281740.3(FHOD3):c.958-89A>G	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1271458	NM_001281740.3(FHOD3):c.958-59T>C	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2648677	NM_001281740.3(FHOD3):c.958-4C>T	FHOD3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3095161	NM_001281740.3(FHOD3):c.972C>G (p.His324Gln)	FHOD3 (H324Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2338505	NM_001281740.3(FHOD3):c.1000C>T (p.Pro334Ser)	FHOD3 (P334S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 791433	NM_001281740.3(FHOD3):c.1005C>A (p.Pro335=)	FHOD3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2367164	NM_001281740.3(FHOD3):c.1009G>A (p.Gly337Arg)	FHOD3 (G337R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095128	NM_001281740.3(FHOD3):c.1010G>A (p.Gly337Glu)	FHOD3 (G337E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1699167	NM_001281740.3(FHOD3):c.1016G>A (p.Arg339Gln)	FHOD3 (R339Q)	Single nucleotide variant (missense variant)	Cardiomyopathy, familial hypertrophic, 28	GUncertain significance
Select item 3095129	NM_001281740.3(FHOD3):c.1021C>T (p.Arg341Trp)	FHOD3 (R341W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2591106	NM_001281740.3(FHOD3):c.1021C>G (p.Arg341Gly)	FHOD3 (R341G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2304331	NM_001281740.3(FHOD3):c.1022G>A (p.Arg341Gln)	FHOD3 (R341Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1231403	NM_001281740.3(FHOD3):c.1035C>T (p.Ser345=)	FHOD3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2285555	NM_001281740.3(FHOD3):c.1046G>C (p.Ser349Thr)	FHOD3 (S349T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2592919	NM_001281740.3(FHOD3):c.1048G>T (p.Gly350Cys)	FHOD3 (G350C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3062011	NM_001281740.3(FHOD3):c.1066G>A (p.Gly356Ser)	FHOD3 (G356S)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2584574	NM_001281740.3(FHOD3):c.1097C>T (p.Ser366Leu)	FHOD3 (S366L)	Single nucleotide variant (missense variant)	Cardiomyopathy, familial hypertrophic, 28 +1 more	GUncertain significance
Select item 3095130	NM_001281740.3(FHOD3):c.1156C>T (p.Pro386Ser)	FHOD3 (P386S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2263373	NM_001281740.3(FHOD3):c.1156C>G (p.Pro386Ala)	FHOD3 (P386A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3053961	NM_001281740.3(FHOD3):c.1172A>G (p.Asn391Ser)	FHOD3 (N391S)	Single nucleotide variant (missense variant)	FHOD3-related disorder	GUncertain significance
Select item 3095131	NM_001281740.3(FHOD3):c.1183G>A (p.Asp395Asn)	FHOD3 (D395N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1273155	NM_001281740.3(FHOD3):c.1197-139dup	FHOD3	Duplication (intron variant)	not provided	GBenign
Select item 1316246	NM_001281740.3(FHOD3):c.1197-138G>T	FHOD3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1244681	NM_001281740.3(FHOD3):c.1197-125dup	FHOD3	Duplication (intron variant)	not provided	GBenign
Select item 1182684	NM_001281740.3(FHOD3):c.1197-137G>T	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3045092	NM_001281740.3(FHOD3):c.1243G>A (p.Glu415Lys)	FHOD3 (E415K)	Single nucleotide variant (missense variant +1 more)	FHOD3-related disorder	GLikely benign
Select item 3037044	NM_001281740.3(FHOD3):c.1248A>G (p.Glu416=)	FHOD3	Single nucleotide variant (synonymous variant +1 more)	FHOD3-related disorder	GLikely benign
Select item 1289568	NM_001281740.3(FHOD3):c.1286+191C>T	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1294079	NM_001281740.3(FHOD3):c.1286+270C>A	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1318301	NM_001281740.3(FHOD3):c.1297G>A (p.Ala433Thr)	FHOD3 (A433T)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 3238795	NM_001281740.3(FHOD3):c.1355C>G (p.Pro452Arg)	FHOD3 (P452R)	Single nucleotide variant (missense variant +1 more)	Cardiomyopathy, familial hypertrophic, 28	GUncertain significance
Select item 1257167	NM_001281740.3(FHOD3):c.1364C>T (p.Ser455Leu)	FHOD3 (S455L)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2648678	NM_001281740.3(FHOD3):c.1383A>G (p.Gly461=)	FHOD3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1274811	NM_001281740.3(FHOD3):c.1411G>A (p.Gly471Arg)	FHOD3 (G471R)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 3048680	NM_001281740.3(FHOD3):c.1489C>T (p.Arg497Trp)	FHOD3 (R497W)	Single nucleotide variant (missense variant +1 more)	FHOD3-related disorder	GLikely benign
Select item 1174142	NM_001281740.3(FHOD3):c.1580_1582del (p.Ser527del)	FHOD3 (S527del)	Deletion (intron variant +1 more)	Cardiomyopathy, familial hypertrophic, 28	GPathogenic
Select item 1174141	NM_001281740.3(FHOD3):c.1583A>G (p.Tyr528Cys)	FHOD3	Single nucleotide variant (missense variant +1 more)	Cardiomyopathy, familial hypertrophic, 28	GLikely pathogenic
Select item 977175	NM_001281740.3(FHOD3):c.1646+1G>A	FHOD3	Single nucleotide variant (splice donor variant +1 more)	Cardiomyopathy, familial hypertrophic, 28	GUncertain significance
Select item 1805290	NM_001281740.3(FHOD3):c.1646+2T>C	FHOD3	Single nucleotide variant (splice donor variant +1 more)	not provided +1 more	GUncertain significance
Select item 1221394	NM_001281740.3(FHOD3):c.1646+60T>C	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1298190	NM_001281740.3(FHOD3):c.1647-74C>T	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3061397	NM_001281740.3(FHOD3):c.1659T>C (p.Ser553=)	FHOD3	Single nucleotide variant (synonymous variant +1 more)	FHOD3-related disorder	GUncertain significance
Select item 1709576	NM_001281740.3(FHOD3):c.1721+1G>A	FHOD3	Single nucleotide variant (splice donor variant +1 more)	Cardiomyopathy, familial hypertrophic, 28	GUncertain significance
Select item 1247462	NM_001281740.3(FHOD3):c.1721+151T>C	FHOD3	Single nucleotide variant (intron variant)	not provided	GBenign

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