ClinVar for Gene (Select 57519) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3357017	NM_020759.3(STARD9):c.10359G>A (p.Gln3453=)	STARD9	Single nucleotide variant (synonymous variant)	STARD9-related disorder	GLikely benign
Select item 3352955	NM_020759.3(STARD9):c.1197T>C (p.Ile399=)	STARD9	Single nucleotide variant (synonymous variant)	STARD9-related disorder	GLikely benign
Select item 3323183	NM_020759.3(STARD9):c.2972G>A (p.Arg991Gln)	STARD9 (R991Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3323182	NM_020759.3(STARD9):c.13772T>C (p.Val4591Ala)	STARD9 (V4591A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323181	NM_020759.3(STARD9):c.7377T>G (p.Ser2459Arg)	STARD9 (S2459R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3323180	NM_020759.3(STARD9):c.2444C>G (p.Thr815Arg)	STARD9 (T815R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323179	NM_020759.3(STARD9):c.5774C>T (p.Thr1925Met)	STARD9 (T1925M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323178	NM_020759.3(STARD9):c.4706A>G (p.Lys1569Arg)	STARD9 (K1569R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323177	NM_020759.3(STARD9):c.12350G>A (p.Cys4117Tyr)	STARD9 (C4117Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323176	NM_020759.3(STARD9):c.7279A>G (p.Ser2427Gly)	STARD9 (S2427G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323175	NM_020759.3(STARD9):c.3629C>T (p.Ala1210Val)	STARD9 (A1210V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323174	NM_020759.3(STARD9):c.1427C>T (p.Ser476Phe)	STARD9 (S476F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323173	NM_020759.3(STARD9):c.11579G>C (p.Ser3860Thr)	STARD9 (S3860T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323172	NM_020759.3(STARD9):c.13240A>G (p.Ser4414Gly)	STARD9 (S4414G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323171	NM_020759.3(STARD9):c.12001C>G (p.Gln4001Glu)	STARD9 (Q4001E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323170	NM_020759.3(STARD9):c.2629T>G (p.Leu877Val)	STARD9 (L877V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323169	NM_020759.3(STARD9):c.3124A>G (p.Lys1042Glu)	STARD9 (K1042E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323168	NM_020759.3(STARD9):c.9815C>G (p.Thr3272Ser)	STARD9 (T3272S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323167	NM_020759.3(STARD9):c.10886C>T (p.Pro3629Leu)	STARD9 (P3629L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323166	NM_020759.3(STARD9):c.13661G>T (p.Arg4554Leu)	STARD9 (R4554L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323165	NM_020759.3(STARD9):c.8233C>T (p.Pro2745Ser)	STARD9 (P2745S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3323164	NM_020759.3(STARD9):c.7785G>T (p.Gln2595His)	STARD9 (Q2595H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323163	NM_020759.3(STARD9):c.7576G>C (p.Val2526Leu)	STARD9 (V2526L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323162	NM_020759.3(STARD9):c.43A>G (p.Lys15Glu)	STARD9 (K15E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323161	NM_020759.3(STARD9):c.12265C>T (p.Pro4089Ser)	STARD9 (P4089S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323160	NM_020759.3(STARD9):c.11966C>G (p.Pro3989Arg)	STARD9 (P3989R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323159	NM_020759.3(STARD9):c.9623C>A (p.Pro3208His)	STARD9 (P3208H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323158	NM_020759.3(STARD9):c.6661A>G (p.Lys2221Glu)	STARD9 (K2221E)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3323157	NM_020759.3(STARD9):c.6679G>T (p.Val2227Leu)	STARD9 (V2227L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323156	NM_020759.3(STARD9):c.6422A>T (p.His2141Leu)	STARD9 (H2141L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323155	NM_020759.3(STARD9):c.1637G>T (p.Arg546Leu)	STARD9 (R546L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323154	NM_020759.3(STARD9):c.1628G>C (p.Arg543Pro)	STARD9 (R543P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323153	NM_020759.3(STARD9):c.4106G>C (p.Cys1369Ser)	STARD9 (C1369S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323152	NM_020759.3(STARD9):c.2803G>A (p.Glu935Lys)	STARD9 (E935K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323151	NM_020759.3(STARD9):c.3080C>T (p.Thr1027Ile)	STARD9 (T1027I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323150	NM_020759.3(STARD9):c.13817G>A (p.Cys4606Tyr)	STARD9 (C4606Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323149	NM_020759.3(STARD9):c.3049C>A (p.Gln1017Lys)	STARD9 (Q1017K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323148	NM_020759.3(STARD9):c.7520A>G (p.Lys2507Arg)	STARD9 (K2507R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323147	NM_020759.3(STARD9):c.3573C>G (p.Asp1191Glu)	STARD9 (D1191E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323146	NM_020759.3(STARD9):c.2776C>T (p.Pro926Ser)	STARD9 (P926S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3323145	NM_020759.3(STARD9):c.11582C>T (p.Pro3861Leu)	STARD9 (P3861L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3323144	NM_020759.3(STARD9):c.1787C>G (p.Ala596Gly)	STARD9 (A596G)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3323143	NM_020759.3(STARD9):c.13210C>A (p.Leu4404Ile)	STARD9 (L4404I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323142	NM_020759.3(STARD9):c.12913C>T (p.Arg4305Cys)	STARD9 (R4305C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323141	NM_020759.3(STARD9):c.9014A>G (p.Tyr3005Cys)	STARD9 (Y3005C)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3323140	NM_020759.3(STARD9):c.11213C>T (p.Thr3738Ile)	STARD9 (T3738I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323139	NM_020759.3(STARD9):c.163A>G (p.Met55Val)	STARD9 (M55V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3323138	NM_020759.3(STARD9):c.1586C>T (p.Thr529Ile)	STARD9 (T529I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323137	NM_020759.3(STARD9):c.4088T>A (p.Met1363Lys)	STARD9 (M1363K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323136	NM_020759.3(STARD9):c.9773C>G (p.Pro3258Arg)	STARD9 (P3258R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323135	NM_020759.3(STARD9):c.9127G>C (p.Glu3043Gln)	STARD9 (E3043Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323134	NM_020759.3(STARD9):c.8971C>T (p.Pro2991Ser)	STARD9 (P2991S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323133	NM_020759.3(STARD9):c.8615A>G (p.Gln2872Arg)	STARD9 (Q2872R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323132	NM_020759.3(STARD9):c.8320C>A (p.Pro2774Thr)	STARD9 (P2774T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323131	NM_020759.3(STARD9):c.7207G>A (p.Ala2403Thr)	STARD9 (A2403T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323130	NM_020759.3(STARD9):c.4141G>A (p.Glu1381Lys)	STARD9 (E1381K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323129	NM_020759.3(STARD9):c.2450C>G (p.Pro817Arg)	STARD9 (P817R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323128	NM_020759.3(STARD9):c.13817G>C (p.Cys4606Ser)	STARD9 (C4606S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323127	NM_020759.3(STARD9):c.12994A>G (p.Thr4332Ala)	STARD9 (T4332A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323126	NM_020759.3(STARD9):c.8713C>T (p.Pro2905Ser)	STARD9 (P2905S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323124	NM_020759.3(STARD9):c.771C>T (p.Ser257=)	STARD9	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3323123	NM_020759.3(STARD9):c.12028G>A (p.Gly4010Arg)	STARD9 (G4010R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323122	NM_020759.3(STARD9):c.11716G>T (p.Ala3906Ser)	STARD9 (A3906S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3239039	NM_020759.3(STARD9):c.5323C>T (p.Pro1775Ser)	STARD9 (P1775S)	Single nucleotide variant (missense variant)	not provided	GLikely benign
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

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