"PreventionGenetics, part of Exact Sciences"[submitter] AND "STARD9"[g - ClinVar

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Items: 56

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2350746	NM_020759.3(STARD9):c.158A>G (p.Lys53Arg)	STARD9 (K53R)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3050407	NM_020759.3(STARD9):c.560-6C>T	STARD9	Single nucleotide variant (intron variant)	STARD9-related disorder	GLikely benign
Select item 3038413	NM_020759.3(STARD9):c.729T>G (p.Ser243=)	STARD9	Single nucleotide variant (synonymous variant)	STARD9-related disorder	GBenign
Select item 2645239	NM_020759.3(STARD9):c.834C>T (p.Ser278=)	STARD9	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1223154	NM_020759.3(STARD9):c.1254+4T>G	STARD9	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 3040598	NM_020759.3(STARD9):c.1649A>G (p.Asn550Ser)	STARD9 (N550S)	Single nucleotide variant (missense variant)	STARD9-related disorder	GBenign
Select item 807220	NM_020759.3(STARD9):c.1655G>T (p.Arg552Leu)	STARD9 (R552L)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 3048356	NM_020759.3(STARD9):c.2928G>A (p.Gly976=)	STARD9	Single nucleotide variant (synonymous variant)	STARD9-related disorder	GLikely benign
Select item 3035131	NM_020759.3(STARD9):c.3340T>C (p.Cys1114Arg)	STARD9 (C1114R)	Single nucleotide variant (missense variant)	STARD9-related disorder	GLikely benign
Select item 2645241	NM_020759.3(STARD9):c.3543T>C (p.Ala1181=)	STARD9	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3060451	NM_020759.3(STARD9):c.3750A>C (p.Ala1250=)	STARD9	Single nucleotide variant (synonymous variant)	STARD9-related disorder	GBenign
Select item 3033845	NM_020759.3(STARD9):c.3896_3913del (p.1287LQPHCE[2])	STARD9	Deletion (inframe deletion)	STARD9-related disorder	GLikely benign
Select item 723690	NM_020759.3(STARD9):c.3884C>T (p.Pro1295Leu)	STARD9 (P1295L)	Single nucleotide variant (missense variant)	STARD9-related disorder +1 more	GBenign
Select item 3059880	NM_020759.3(STARD9):c.3900G>A (p.Gln1300=)	STARD9	Single nucleotide variant (synonymous variant)	STARD9-related disorder	GBenign
Select item 3035250	NM_020759.3(STARD9):c.4365A>C (p.Glu1455Asp)	STARD9 (E1455D)	Single nucleotide variant (missense variant)	STARD9-related disorder	GLikely benign
Select item 3034224	NM_020759.3(STARD9):c.4641T>C (p.Phe1547=)	STARD9	Single nucleotide variant (synonymous variant)	STARD9-related disorder	GLikely benign
Select item 769878	NM_020759.3(STARD9):c.4650T>A (p.His1550Gln)	STARD9 (H1550Q)	Single nucleotide variant (missense variant)	STARD9-related disorder +1 more	GBenign
Select item 3055214	NM_020759.3(STARD9):c.4675G>T (p.Ala1559Ser)	STARD9 (A1559S)	Single nucleotide variant (missense variant)	STARD9-related disorder	GUncertain significance
Select item 2344335	NM_020759.3(STARD9):c.5116A>G (p.Lys1706Glu)	STARD9 (K1706E)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3055296	NM_020759.3(STARD9):c.6247G>A (p.Glu2083Lys)	STARD9 (E2083K)	Single nucleotide variant (missense variant)	STARD9-related disorder	GBenign
Select item 791193	NM_020759.3(STARD9):c.6309C>T (p.Ser2103=)	STARD9	Single nucleotide variant (synonymous variant)	STARD9-related disorder +1 more	GBenign
Select item 3058964	NM_020759.3(STARD9):c.7246A>G (p.Met2416Val)	STARD9 (M2416V)	Single nucleotide variant (missense variant)	STARD9-related disorder	GBenign
Select item 3059971	NM_020759.3(STARD9):c.8030G>A (p.Arg2677His)	STARD9 (R2677H)	Single nucleotide variant (missense variant)	STARD9-related disorder	GBenign
Select item 3044644	NM_020759.3(STARD9):c.8274T>C (p.His2758=)	STARD9	Single nucleotide variant (synonymous variant)	STARD9-related disorder	GLikely benign
Select item 3048493	NM_020759.3(STARD9):c.8301G>T (p.Glu2767Asp)	STARD9 (E2767D)	Single nucleotide variant (missense variant)	STARD9-related disorder	GBenign
Select item 769880	NM_020759.3(STARD9):c.8348A>G (p.His2783Arg)	STARD9 (H2783R)	Single nucleotide variant (missense variant)	STARD9-related disorder +1 more	GBenign
Select item 3048478	NM_020759.3(STARD9):c.8367A>G (p.Leu2789=)	STARD9	Single nucleotide variant (synonymous variant)	STARD9-related disorder	GLikely benign
Select item 3035320	NM_020759.3(STARD9):c.8461G>C (p.Val2821Leu)	STARD9 (V2821L)	Single nucleotide variant (missense variant)	STARD9-related disorder	GLikely benign
Select item 3060020	NM_020759.3(STARD9):c.8564C>T (p.Thr2855Ile)	STARD9 (T2855I)	Single nucleotide variant (missense variant)	STARD9-related disorder	GBenign
Select item 3045536	NM_020759.3(STARD9):c.9136A>G (p.Thr3046Ala)	STARD9 (T3046A)	Single nucleotide variant (missense variant)	STARD9-related disorder	GLikely benign
Select item 3045612	NM_020759.3(STARD9):c.9192C>T (p.Asp3064=)	STARD9	Single nucleotide variant (synonymous variant)	STARD9-related disorder	GLikely benign
Select item 3058528	NM_020759.3(STARD9):c.9381G>C (p.Val3127=)	STARD9	Single nucleotide variant (synonymous variant)	STARD9-related disorder	GLikely benign
Select item 3041242	NM_020759.3(STARD9):c.9388A>G (p.Thr3130Ala)	STARD9 (T3130A)	Single nucleotide variant (missense variant)	STARD9-related disorder	GUncertain significance
Select item 3056400	NM_020759.3(STARD9):c.9680C>T (p.Ala3227Val)	STARD9 (A3227V)	Single nucleotide variant (missense variant)	STARD9-related disorder	GUncertain significance
Select item 2212235	NM_020759.3(STARD9):c.9796G>A (p.Gly3266Ser)	STARD9 (G3266S)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3046376	NM_020759.3(STARD9):c.9977T>G (p.Phe3326Cys)	STARD9 (F3326C)	Single nucleotide variant (missense variant)	STARD9-related disorder	GLikely benign
Select item 3057242	NM_020759.3(STARD9):c.10026G>A (p.Val3342=)	STARD9	Single nucleotide variant (synonymous variant)	STARD9-related disorder	GLikely benign
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 3048761	NM_020759.3(STARD9):c.10206T>C (p.Pro3402=)	STARD9	Single nucleotide variant (synonymous variant)	STARD9-related disorder	GLikely benign
Select item 3035223	NM_020759.3(STARD9):c.10245C>T (p.His3415=)	STARD9	Single nucleotide variant (synonymous variant)	STARD9-related disorder	GLikely benign
Select item 2635301	NM_020759.3(STARD9):c.10315G>A (p.Glu3439Lys)	STARD9 (E3439K)	Single nucleotide variant (missense variant)	STARD9-related disorder	GUncertain significance
Select item 1325596	NM_020759.3(STARD9):c.10480G>A (p.Val3494Ile)	STARD9 (V3494I)	Single nucleotide variant (missense variant)	STARD9-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 3053736	NM_020759.3(STARD9):c.10551C>T (p.Gly3517=)	STARD9	Single nucleotide variant (synonymous variant)	STARD9-related disorder	GLikely benign
Select item 3031673	NM_020759.3(STARD9):c.10897A>G (p.Thr3633Ala)	STARD9 (T3633A)	Single nucleotide variant (missense variant)	STARD9-related disorder	GUncertain significance
Select item 3039249	NM_020759.3(STARD9):c.11289G>A (p.Gly3763=)	STARD9	Single nucleotide variant (synonymous variant)	STARD9-related disorder	GLikely benign
Select item 3042767	NM_020759.3(STARD9):c.11307G>A (p.Ser3769=)	STARD9	Single nucleotide variant (synonymous variant)	STARD9-related disorder	GLikely benign
Select item 3045760	NM_020759.3(STARD9):c.11336C>T (p.Pro3779Leu)	STARD9 (P3779L)	Single nucleotide variant (missense variant)	STARD9-related disorder	GLikely benign
Select item 3044998	NM_020759.3(STARD9):c.11411G>A (p.Ser3804Asn)	STARD9 (S3804N)	Single nucleotide variant (missense variant)	STARD9-related disorder	GLikely benign
Select item 3051683	NM_020759.3(STARD9):c.12027C>T (p.Ile4009=)	STARD9	Single nucleotide variant (synonymous variant)	STARD9-related disorder	GLikely benign
Select item 724264	NM_020759.3(STARD9):c.12033C>G (p.Val4011=)	STARD9	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 770244	NM_020759.3(STARD9):c.12097C>T (p.Pro4033Ser)	STARD9 (P4033S)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 3054494	NM_020759.3(STARD9):c.12117G>A (p.Pro4039=)	STARD9	Single nucleotide variant (synonymous variant)	STARD9-related disorder	GLikely benign
Select item 3035067	NM_020759.3(STARD9):c.12594C>T (p.Pro4198=)	STARD9	Single nucleotide variant (synonymous variant)	STARD9-related disorder	GLikely benign
Select item 3051871	NM_020759.3(STARD9):c.12672C>T (p.Ala4224=)	STARD9	Single nucleotide variant (synonymous variant)	STARD9-related disorder	GLikely benign
Select item 3033950	NM_020759.3(STARD9):c.12789C>T (p.Leu4263=)	STARD9	Single nucleotide variant (synonymous variant)	STARD9-related disorder	GLikely benign
Select item 3043573	NM_020759.3(STARD9):c.13241G>A (p.Ser4414Asn)	STARD9 (S4414N)	Single nucleotide variant (missense variant)	STARD9-related disorder	GBenign

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Items: 56