"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "STARD9"[ge - ClinVar

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 718236	NM_020759.3(STARD9):c.719A>G (p.Asn240Ser)	STARD9 (N240S)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2645239	NM_020759.3(STARD9):c.834C>T (p.Ser278=)	STARD9	Single nucleotide variant (synonymous variant)	STARD9-related condition +1 more	GLikely benign
Select item 807219	NM_020759.3(STARD9):c.994T>C (p.Ser332Pro)	STARD9 (S332P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1675567	NM_020759.3(STARD9):c.1101C>G (p.Ser367Arg)	STARD9 (S367R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2645240	NM_020759.3(STARD9):c.1411G>C (p.Gly471Arg)	STARD9 (G471R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
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 807221	NM_020759.3(STARD9):c.3302C>T (p.Ser1101Phe)	STARD9 (S1101F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
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 807222	NM_020759.3(STARD9):c.3568T>C (p.Ser1190Pro)	STARD9 (S1190P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2645242	NM_020759.3(STARD9):c.4367C>T (p.Ala1456Val)	STARD9 (A1456V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 733003	NM_020759.3(STARD9):c.5957G>A (p.Arg1986His)	STARD9 (R1986H)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2645243	NM_020759.3(STARD9):c.6519G>A (p.Ser2173=)	STARD9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1675568	NM_020759.3(STARD9):c.6521A>G (p.Asp2174Gly)	STARD9 (D2174G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2356305	NM_020759.3(STARD9):c.7154C>T (p.Thr2385Met)	STARD9 (T2385M)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2645244	NM_020759.3(STARD9):c.7325C>G (p.Pro2442Arg)	STARD9 (P2442R)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2508654	NM_020759.3(STARD9):c.7444G>T (p.Val2482Phe)	STARD9 (V2482F)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 807223	NM_020759.3(STARD9):c.7968C>G (p.Asp2656Glu)	STARD9 (D2656E)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 712187	NM_020759.3(STARD9):c.8314A>G (p.Ile2772Val)	STARD9 (I2772V)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2645245	NM_020759.3(STARD9):c.8609C>T (p.Thr2870Ile)	STARD9 (T2870I)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2379036	NM_020759.3(STARD9):c.8932A>G (p.Arg2978Gly)	STARD9 (R2978G)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2645246	NM_020759.3(STARD9):c.9115A>C (p.Ser3039Arg)	STARD9 (S3039R)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1675569	NM_020759.3(STARD9):c.10380C>G (p.His3460Gln)	STARD9 (H3460Q)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2645247	NM_020759.3(STARD9):c.10869A>G (p.Pro3623=)	STARD9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3025802	NM_020759.3(STARD9):c.11322A>C (p.Glu3774Asp)	STARD9 (E3774D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2645248	NM_020759.3(STARD9):c.12174T>C (p.Asn4058=)	STARD9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 778489	NM_020759.3(STARD9):c.12223C>A (p.Arg4075=)	STARD9	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2645249	NM_020759.3(STARD9):c.12621A>G (p.Ser4207=)	STARD9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2645250	NM_020759.3(STARD9):c.12638_12639del (p.Thr4213fs)	STARD9 (T4213fs)	Microsatellite (frameshift variant)	not provided	GUncertain significance
Select item 2645251	NM_020759.3(STARD9):c.12787C>T (p.Leu4263Phe)	STARD9 (L4263F)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 807224	NM_020759.3(STARD9):c.13147-3C>A	STARD9	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2645252	NM_020759.3(STARD9):c.13445C>T (p.Ser4482Phe)	STARD9 (S4482F)	Single nucleotide variant (missense variant)	not provided	GLikely benign

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Items: 31