SYT10[gene] and "single gene"[properties] - ClinVar

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Items: 38

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2386076	NM_198992.4(SYT10):c.1555C>A (p.Pro519Thr)	SYT10 (P519T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267864	NM_198992.4(SYT10):c.1549C>G (p.Pro517Ala)	SYT10 (P517A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 787922	NM_198992.4(SYT10):c.1514C>T (p.Ala505Val)	SYT10 (A505V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2307219	NM_198992.4(SYT10):c.1423G>A (p.Gly475Ser)	SYT10 (G475S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376124	NM_198992.4(SYT10):c.1420G>A (p.Glu474Lys)	SYT10 (E474K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290665	NM_198992.4(SYT10):c.1375G>A (p.Gly459Arg)	SYT10 (G459R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2642844	NM_198992.4(SYT10):c.1368T>C (p.Asp456=)	SYT10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 714177	NM_198992.4(SYT10):c.1259C>G (p.Thr420Ser)	SYT10 (T420S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2324698	NM_198992.4(SYT10):c.1232G>A (p.Gly411Asp)	SYT10 (G411D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172940	NM_198992.4(SYT10):c.1230A>C (p.Glu410Asp)	SYT10 (E410D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612678	NM_198992.4(SYT10):c.1210A>G (p.Lys404Glu)	SYT10 (K404E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462693	NM_198992.4(SYT10):c.1175C>T (p.Ala392Val)	SYT10 (A392V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225252	NM_198992.4(SYT10):c.1079A>G (p.Glu360Gly)	SYT10 (E360G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3324017	NM_198992.4(SYT10):c.1015T>C (p.Phe339Leu)	SYT10 (F339L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475833	NM_198992.4(SYT10):c.859G>A (p.Val287Met)	SYT10 (V287M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172948	NM_198992.4(SYT10):c.856C>A (p.Arg286Ser)	SYT10 (R286S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530989	NM_198992.4(SYT10):c.842A>C (p.Lys281Thr)	SYT10 (K281T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304255	NM_198992.4(SYT10):c.832G>T (p.Asp278Tyr)	SYT10 (D278Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172947	NM_198992.4(SYT10):c.702A>C (p.Lys234Asn)	SYT10 (K234N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3324018	NM_198992.4(SYT10):c.641A>G (p.Tyr214Cys)	SYT10 (Y214C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300125	NM_198992.4(SYT10):c.528A>T (p.Arg176Ser)	SYT10 (R176S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282813	NM_198992.4(SYT10):c.502T>A (p.Ser168Thr)	SYT10 (S168T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382673	NM_198992.4(SYT10):c.461A>G (p.Lys154Arg)	SYT10 (K154R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335403	NM_198992.4(SYT10):c.386C>G (p.Pro129Arg)	SYT10 (P129R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232966	NM_198992.4(SYT10):c.376G>A (p.Ala126Thr)	SYT10 (A126T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 768537	NM_198992.4(SYT10):c.369C>T (p.Ala123=)	SYT10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2306638	NM_198992.4(SYT10):c.339A>C (p.Lys113Asn)	SYT10 (K113N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172945	NM_198992.4(SYT10):c.284C>T (p.Thr95Met)	SYT10 (T95M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172944	NM_198992.4(SYT10):c.240T>G (p.Cys80Trp)	SYT10 (C80W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2230487	NM_198992.4(SYT10):c.229T>C (p.Trp77Arg)	SYT10 (W77R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172943	NM_198992.4(SYT10):c.186C>A (p.Ser62Arg)	SYT10 (S62R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595554	NM_198992.4(SYT10):c.178G>A (p.Val60Ile)	SYT10 (V60I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172942	NM_198992.4(SYT10):c.146G>T (p.Ser49Ile)	SYT10 (S49I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352128	NM_198992.4(SYT10):c.77C>T (p.Ala26Val)	SYT10 (A26V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459751	NM_198992.4(SYT10):c.74T>G (p.Phe25Cys)	SYT10 (F25C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172946	NM_198992.4(SYT10):c.37T>A (p.Cys13Ser)	SYT10 (C13S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607729	NM_198992.4(SYT10):c.34C>G (p.Leu12Val)	SYT10 (L12V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 394935	GRCh37/hg19 12p11.1(chr12:33528404-33579087)x3	SYT10	Copy number gain	See cases	GBenign

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Items: 38