ClinVar for Gene (Select 57519) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3171108	NM_020759.3(STARD9):c.9881G>A (p.Gly3294Asp)	STARD9 (G3294D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171107	NM_020759.3(STARD9):c.9679G>T (p.Ala3227Ser)	STARD9 (A3227S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171106	NM_020759.3(STARD9):c.9556C>T (p.Arg3186Cys)	STARD9 (R3186C)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3171105	NM_020759.3(STARD9):c.949T>C (p.Ser317Pro)	STARD9 (S317P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171104	NM_020759.3(STARD9):c.9331C>T (p.Pro3111Ser)	STARD9 (P3111S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171103	NM_020759.3(STARD9):c.9296A>C (p.Glu3099Ala)	STARD9 (E3099A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171102	NM_020759.3(STARD9):c.9193G>A (p.Val3065Met)	STARD9 (V3065M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171101	NM_020759.3(STARD9):c.9116G>A (p.Ser3039Asn)	STARD9 (S3039N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171100	NM_020759.3(STARD9):c.8890A>C (p.Thr2964Pro)	STARD9 (T2964P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171099	NM_020759.3(STARD9):c.8861G>A (p.Arg2954Gln)	STARD9 (R2954Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3171098	NM_020759.3(STARD9):c.8832A>C (p.Arg2944Ser)	STARD9 (R2944S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171097	NM_020759.3(STARD9):c.8420A>G (p.Glu2807Gly)	STARD9 (E2807G)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3171096	NM_020759.3(STARD9):c.8394T>A (p.Asp2798Glu)	STARD9 (D2798E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171095	NM_020759.3(STARD9):c.8135C>T (p.Pro2712Leu)	STARD9 (P2712L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3171094	NM_020759.3(STARD9):c.8057C>T (p.Ala2686Val)	STARD9 (A2686V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171093	NM_020759.3(STARD9):c.778G>A (p.Ala260Thr)	STARD9 (A260T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171091	NM_020759.3(STARD9):c.772G>A (p.Glu258Lys)	STARD9 (E258K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171090	NM_020759.3(STARD9):c.7557C>A (p.Ser2519Arg)	STARD9 (S2519R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171089	NM_020759.3(STARD9):c.7235G>A (p.Arg2412Gln)	STARD9 (R2412Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171088	NM_020759.3(STARD9):c.7196G>C (p.Arg2399Pro)	STARD9 (R2399P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171086	NM_020759.3(STARD9):c.7055C>T (p.Ala2352Val)	STARD9 (A2352V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3171085	NM_020759.3(STARD9):c.7042C>T (p.His2348Tyr)	STARD9 (H2348Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171084	NM_020759.3(STARD9):c.686C>T (p.Thr229Met)	STARD9 (T229M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171083	NM_020759.3(STARD9):c.6848G>A (p.Gly2283Glu)	STARD9 (G2283E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171082	NM_020759.3(STARD9):c.6716G>A (p.Gly2239Asp)	STARD9 (G2239D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171081	NM_020759.3(STARD9):c.6626C>G (p.Ala2209Gly)	STARD9 (A2209G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171080	NM_020759.3(STARD9):c.6205A>C (p.Asn2069His)	STARD9 (N2069H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171079	NM_020759.3(STARD9):c.6151A>G (p.Ile2051Val)	STARD9 (I2051V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171078	NM_020759.3(STARD9):c.5993G>A (p.Gly1998Asp)	STARD9 (G1998D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171077	NM_020759.3(STARD9):c.5795A>G (p.Asn1932Ser)	STARD9 (N1932S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171076	NM_020759.3(STARD9):c.5561A>G (p.Asn1854Ser)	STARD9 (N1854S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171075	NM_020759.3(STARD9):c.5474C>T (p.Thr1825Ile)	STARD9 (T1825I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171074	NM_020759.3(STARD9):c.5396C>T (p.Pro1799Leu)	STARD9 (P1799L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171073	NM_020759.3(STARD9):c.5359C>G (p.Gln1787Glu)	STARD9 (Q1787E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171072	NM_020759.3(STARD9):c.5177A>G (p.Tyr1726Cys)	STARD9 (Y1726C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171071	NM_020759.3(STARD9):c.5077C>G (p.Pro1693Ala)	STARD9 (P1693A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171070	NM_020759.3(STARD9):c.4904G>A (p.Ser1635Asn)	STARD9 (S1635N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171068	NM_020759.3(STARD9):c.4808C>G (p.Thr1603Arg)	STARD9 (T1603R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171067	NM_020759.3(STARD9):c.4772C>T (p.Ser1591Leu)	STARD9 (S1591L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171066	NM_020759.3(STARD9):c.4745A>T (p.Lys1582Ile)	STARD9 (K1582I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171065	NM_020759.3(STARD9):c.4106G>A (p.Cys1369Tyr)	STARD9 (C1369Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171064	NM_020759.3(STARD9):c.401A>G (p.Glu134Gly)	STARD9 (E134G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171063	NM_020759.3(STARD9):c.3955G>A (p.Asp1319Asn)	STARD9 (D1319N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3171062	NM_020759.3(STARD9):c.3830T>G (p.Leu1277Arg)	STARD9 (L1277R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171061	NM_020759.3(STARD9):c.378A>G (p.Ile126Met)	STARD9 (I126M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171060	NM_020759.3(STARD9):c.3685G>A (p.Glu1229Lys)	STARD9 (E1229K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171058	NM_020759.3(STARD9):c.3534A>T (p.Arg1178Ser)	STARD9 (R1178S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171057	NM_020759.3(STARD9):c.3499C>T (p.Arg1167Cys)	STARD9 (R1167C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171056	NM_020759.3(STARD9):c.3220A>G (p.Thr1074Ala)	STARD9 (T1074A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3171055	NM_020759.3(STARD9):c.2801T>C (p.Met934Thr)	STARD9 (M934T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171054	NM_020759.3(STARD9):c.2732C>A (p.Ala911Asp)	STARD9 (A911D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171053	NM_020759.3(STARD9):c.2671C>T (p.Arg891Cys)	STARD9 (R891C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171051	NM_020759.3(STARD9):c.2360G>A (p.Arg787Lys)	STARD9 (R787K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171050	NM_020759.3(STARD9):c.2306C>T (p.Ser769Leu)	STARD9 (S769L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171049	NM_020759.3(STARD9):c.206A>G (p.Glu69Gly)	STARD9 (E69G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171048	NM_020759.3(STARD9):c.2009G>A (p.Arg670Gln)	STARD9 (R670Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3171047	NM_020759.3(STARD9):c.1880C>T (p.Ala627Val)	STARD9 (A627V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3171046	NM_020759.3(STARD9):c.1840C>T (p.Arg614Trp)	STARD9 (R614W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171045	NM_020759.3(STARD9):c.1792C>T (p.Arg598Cys)	STARD9 (R598C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171044	NM_020759.3(STARD9):c.1772T>A (p.Val591Asp)	STARD9 (V591D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171043	NM_020759.3(STARD9):c.1655G>A (p.Arg552Gln)	STARD9 (R552Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171042	NM_020759.3(STARD9):c.1631G>C (p.Gly544Ala)	STARD9 (G544A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171041	NM_020759.3(STARD9):c.14036T>A (p.Leu4679His)	STARD9 (L4679H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171040	NM_020759.3(STARD9):c.13778A>C (p.Asn4593Thr)	STARD9 (N4593T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171039	NM_020759.3(STARD9):c.13414A>G (p.Ser4472Gly)	STARD9 (S4472G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171038	NM_020759.3(STARD9):c.13298T>G (p.Leu4433Trp)	STARD9 (L4433W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171037	NM_020759.3(STARD9):c.13192A>G (p.Thr4398Ala)	STARD9 (T4398A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171036	NM_020759.3(STARD9):c.13121A>G (p.Gln4374Arg)	STARD9 (Q4374R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171035	NM_020759.3(STARD9):c.13091G>A (p.Arg4364Gln)	STARD9 (R4364Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3171034	NM_020759.3(STARD9):c.13090C>T (p.Arg4364Trp)	STARD9 (R4364W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171033	NM_020759.3(STARD9):c.12895C>T (p.Leu4299Phe)	STARD9 (L4299F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171031	NM_020759.3(STARD9):c.12713C>T (p.Ala4238Val)	STARD9 (A4238V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171030	NM_020759.3(STARD9):c.12581G>A (p.Arg4194Lys)	STARD9 (R4194K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171029	NM_020759.3(STARD9):c.124A>T (p.Asn42Tyr)	STARD9 (N42Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171028	NM_020759.3(STARD9):c.12457C>G (p.Pro4153Ala)	STARD9 (P4153A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171026	NM_020759.3(STARD9):c.12224G>A (p.Arg4075Gln)	STARD9 (R4075Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171025	NM_020759.3(STARD9):c.12221A>G (p.Asp4074Gly)	STARD9 (D4074G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171024	NM_020759.3(STARD9):c.12211C>T (p.Arg4071Cys)	STARD9 (R4071C)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3171023	NM_020759.3(STARD9):c.12208C>A (p.Gln4070Lys)	STARD9 (Q4070K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171022	NM_020759.3(STARD9):c.12092T>G (p.Phe4031Cys)	STARD9 (F4031C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171021	NM_020759.3(STARD9):c.12053C>G (p.Pro4018Arg)	STARD9 (P4018R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171020	NM_020759.3(STARD9):c.11945C>T (p.Pro3982Leu)	STARD9 (P3982L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171019	NM_020759.3(STARD9):c.11827G>T (p.Ala3943Ser)	STARD9 (A3943S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171017	NM_020759.3(STARD9):c.11180C>T (p.Ser3727Phe)	STARD9 (S3727F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171016	NM_020759.3(STARD9):c.11168T>A (p.Met3723Lys)	STARD9 (M3723K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171015	NM_020759.3(STARD9):c.11144C>A (p.Pro3715Gln)	STARD9 (P3715Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171014	NM_020759.3(STARD9):c.11068A>G (p.Ser3690Gly)	STARD9 (S3690G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171013	NM_020759.3(STARD9):c.11062C>A (p.Leu3688Met)	STARD9 (L3688M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171012	NM_020759.3(STARD9):c.10936G>A (p.Gly3646Ser)	STARD9 (G3646S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171011	NM_020759.3(STARD9):c.10888G>T (p.Val3630Leu)	STARD9 (V3630L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171010	NM_020759.3(STARD9):c.10654A>G (p.Asn3552Asp)	STARD9 (N3552D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171009	NM_020759.3(STARD9):c.10580C>G (p.Ser3527Cys)	STARD9 (S3527C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171007	NM_020759.3(STARD9):c.10544A>G (p.Asp3515Gly)	STARD9 (D3515G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171006	NM_020759.3(STARD9):c.10477G>T (p.Asp3493Tyr)	STARD9 (D3493Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171005	NM_020759.3(STARD9):c.10475T>C (p.Val3492Ala)	STARD9 (V3492A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171004	NM_020759.3(STARD9):c.10409C>T (p.Ala3470Val)	STARD9 (A3470V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3171003	NM_020759.3(STARD9):c.10409C>A (p.Ala3470Glu)	STARD9 (A3470E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063379	GRCh37/hg19 15q11.2-21.2(chr15:22770421-50347130)x3	ACTC1, ADAL +200 more	Copy number gain	not specified	GPathogenic
Select item 3060766	NM_020759.3(STARD9):c.10147A>G (p.Asn3383Asp)	STARD9 (N3383D)	Single nucleotide variant (missense variant)	STARD9-related disorder	GBenign
Select item 3060451	NM_020759.3(STARD9):c.3750A>C (p.Ala1250=)	STARD9	Single nucleotide variant (synonymous variant)	STARD9-related disorder	GBenign

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