ClinVar for Gene (Select 60681) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3351106	NM_021939.4(FKBP10):c.479C>T (p.Thr160Ile)	FKBP10 (T160I)	Single nucleotide variant (missense variant)	FKBP10-related disorder	GUncertain significance
Select item 3278930	NM_021939.4(FKBP10):c.1405G>A (p.Gly469Arg)	FKBP10 (G469R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3278929	NM_021939.4(FKBP10):c.314G>C (p.Gly105Ala)	FKBP10 (G105A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3278928	NM_021939.4(FKBP10):c.118C>T (p.Pro40Ser)	FKBP10 (P40S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3278927	NM_021939.4(FKBP10):c.1279G>C (p.Glu427Gln)	FKBP10 (E427Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3278926	NM_021939.4(FKBP10):c.539A>T (p.His180Leu)	FKBP10 (H180L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3278925	NM_021939.4(FKBP10):c.1267G>A (p.Gly423Arg)	FKBP10 (G423R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3278923	NM_021939.4(FKBP10):c.1241C>T (p.Thr414Ile)	FKBP10 (T414I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3278922	NM_021939.4(FKBP10):c.573C>G (p.Phe191Leu)	FKBP10 (F191L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3243203	NC_000017.10:g.(?_39973290)_(39977361_?)del	FKBP10	Deletion	not provided	GPathogenic
Select item 3243202	NC_000017.10:g.(?_39973290)_(39974799_?)del	FKBP10	Deletion	not provided	GPathogenic
Select item 3243201	NC_000017.10:g.(?_39973290)_(39973475_?)del	FKBP10	Deletion	not provided	GPathogenic
Select item 3234921	NM_021939.4(FKBP10):c.1619_1623delinsT (p.Gly540fs)	FKBP10 (G540fs)	Indel (frameshift variant)	Osteogenesis imperfecta type 11	GLikely pathogenic
Select item 3095289	NM_021939.4(FKBP10):c.918C>T (p.Ser306=)	FKBP10	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3095288	NM_021939.4(FKBP10):c.588T>G (p.Ser196Arg)	FKBP10 (S196R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095287	NM_021939.4(FKBP10):c.322G>A (p.Gly108Ser)	FKBP10 (G108S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095286	NM_021939.4(FKBP10):c.176T>C (p.Val59Ala)	FKBP10 (V59A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095285	NM_021939.4(FKBP10):c.1291G>A (p.Gly431Arg)	FKBP10 (G431R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3065529	NM_021939.4(FKBP10):c.884G>T (p.Gly295Val)	FKBP10 (G295V)	Single nucleotide variant (missense variant)	Osteogenesis imperfecta type 11	GUncertain significance
Select item 3065462	NM_021939.4(FKBP10):c.583T>C (p.Tyr195His)	FKBP10 (Y195H)	Single nucleotide variant (missense variant)	Osteogenesis imperfecta type 11	GUncertain significance
Select item 3064485	NM_021939.4(FKBP10):c.392-3C>G	FKBP10	Single nucleotide variant (intron variant)	Osteogenesis imperfecta type 11	GUncertain significance
Select item 3063506	GRCh37/hg19 17q21.2(chr17:39705863-40358580)x3	ACLY, CNP +25 more	Copy number gain	not specified	GUncertain significance
Select item 3031108	NM_021939.4(FKBP10):c.346C>T (p.Arg116Cys)	FKBP10 (R116C)	Single nucleotide variant (missense variant)	FKBP10-related disorder	GUncertain significance
Select item 3030234	NM_021939.4(FKBP10):c.*10A>T	FKBP10	Single nucleotide variant (3 prime UTR variant)	FKBP10-related disorder	GLikely benign
Select item 3023891	NM_021939.4(FKBP10):c.618C>T (p.Gly206=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3017263	NM_021939.4(FKBP10):c.384C>T (p.Ile128=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3013230	NM_021939.4(FKBP10):c.1257-7C>T	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3013216	NM_021939.4(FKBP10):c.90G>T (p.Gly30=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3012707	NM_021939.4(FKBP10):c.1399+17A>T	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3011951	NM_021939.4(FKBP10):c.1564-9C>T	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3010763	NM_021939.4(FKBP10):c.917+8G>A	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3008916	NM_021939.4(FKBP10):c.1256+8_1256+9insCG	FKBP10	Insertion (intron variant)	not provided	GLikely benign
Select item 3007040	NM_021939.4(FKBP10):c.1256+9G>C	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3006487	NM_021939.4(FKBP10):c.1272C>A (p.Ala424=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3005844	NM_021939.4(FKBP10):c.582-20C>G	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3004782	NM_021939.4(FKBP10):c.816G>C (p.Thr272=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3002128	NM_021939.4(FKBP10):c.1063+20A>T	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3002030	NM_021939.4(FKBP10):c.1628del (p.Pro543fs)	FKBP10 (P543fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 3000849	NM_021939.4(FKBP10):c.609C>T (p.Thr203=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2999982	NM_021939.4(FKBP10):c.45C>G (p.Pro15=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2998723	NM_021939.4(FKBP10):c.168C>G (p.Pro56=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2996999	NM_021939.4(FKBP10):c.727+2del	FKBP10	Deletion (splice donor variant)	not provided	GLikely pathogenic
Select item 2996733	NM_021939.4(FKBP10):c.1563+17T>C	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2996465	NM_021939.4(FKBP10):c.1671C>T (p.Asn557=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2996099	NM_021939.4(FKBP10):c.1256+13G>A	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2995855	NM_021939.4(FKBP10):c.226G>A (p.Gly76Ser)	FKBP10 (G76S)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2995680	NM_021939.4(FKBP10):c.1035G>A (p.Pro345=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2994534	NM_021939.4(FKBP10):c.798C>T (p.Asp266=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2992788	NM_021939.4(FKBP10):c.246-7C>T	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2990972	NM_021939.4(FKBP10):c.567C>G (p.Thr189=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2989938	NM_021939.4(FKBP10):c.630G>C (p.Leu210=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2989393	NM_021939.4(FKBP10):c.1278G>A (p.Gln426=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2989392	NM_021939.4(FKBP10):c.1090C>T (p.Leu364=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2988140	NM_021939.4(FKBP10):c.1284G>A (p.Ala428=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2987052	NM_021939.4(FKBP10):c.495C>T (p.Pro165=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2986729	NM_021939.4(FKBP10):c.855C>T (p.Ala285=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2984570	NM_021939.4(FKBP10):c.1256+6dup	FKBP10	Duplication (intron variant)	not provided	GLikely benign
Select item 2983906	NM_021939.4(FKBP10):c.391+10G>A	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2983782	NM_021939.4(FKBP10):c.348C>T (p.Arg116=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2981130	NM_021939.4(FKBP10):c.392-13T>C	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2980342	NM_021939.4(FKBP10):c.561C>T (p.Asp187=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2979547	NM_021939.4(FKBP10):c.1032C>G (p.Pro344=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2979248	NM_021939.4(FKBP10):c.246-4C>A	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2978215	NM_021939.4(FKBP10):c.1596G>A (p.Glu532=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2977670	NM_021939.4(FKBP10):c.1449G>C (p.Val483=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2977094	NM_021939.4(FKBP10):c.1064-20C>T	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2976280	NM_021939.4(FKBP10):c.246-6C>A	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2975908	NM_021939.4(FKBP10):c.246-11T>C	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2975782	NM_021939.4(FKBP10):c.816G>A (p.Thr272=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2975110	NM_021939.4(FKBP10):c.1256+12G>A	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2974492	NM_021939.4(FKBP10):c.1256+18C>G	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2974482	NM_021939.4(FKBP10):c.780C>T (p.Asp260=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2972468	NM_021939.4(FKBP10):c.392-11C>T	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2970884	NM_021939.4(FKBP10):c.1620G>C (p.Gly540=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2970666	NM_021939.4(FKBP10):c.540C>T (p.His180=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2970338	NM_021939.4(FKBP10):c.357G>C (p.Val119=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2970201	NM_021939.4(FKBP10):c.1063+8C>T	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2968952	NM_021939.4(FKBP10):c.150C>T (p.His50=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2967807	NM_021939.4(FKBP10):c.1564-19C>T	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2967680	NM_021939.4(FKBP10):c.1050G>A (p.Gly350=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2966551	NM_021939.4(FKBP10):c.945C>T (p.Thr315=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2966203	NM_021939.4(FKBP10):c.582-14C>T	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2966039	NM_021939.4(FKBP10):c.771C>T (p.Leu257=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2965176	NM_021939.4(FKBP10):c.1194T>C (p.Leu398=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2964996	NM_021939.4(FKBP10):c.246-7C>A	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2962001	NM_021939.4(FKBP10):c.909C>T (p.Phe303=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2961997	NM_021939.4(FKBP10):c.1064-18C>A	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2961802	NM_021939.4(FKBP10):c.582-18C>T	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2959822	NM_021939.4(FKBP10):c.917+12C>T	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2957890	NM_021939.4(FKBP10):c.636G>A (p.Lys212=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2956865	NM_021939.4(FKBP10):c.1256+9G>T	FKBP10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2920884	NM_021939.4(FKBP10):c.1373C>T (p.Pro458Leu)	FKBP10 (P458L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2917713	NM_021939.4(FKBP10):c.279G>A (p.Val93=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2912188	NM_021939.4(FKBP10):c.594C>T (p.Gly198=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2910427	NM_021939.4(FKBP10):c.1276del (p.Gln426fs)	FKBP10 (Q426fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2907756	NM_021939.4(FKBP10):c.15C>T (p.Gly5=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2906252	NM_021939.4(FKBP10):c.1695C>T (p.Asp565=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2906074	NM_021939.4(FKBP10):c.61C>T (p.Leu21=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2906073	NM_021939.4(FKBP10):c.1465C>T (p.Leu489=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2903904	NM_021939.4(FKBP10):c.1218C>T (p.Tyr406=)	FKBP10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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