"Ambry Genetics"[submitter] AND "TSGA10IP"[gene] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2277024	NM_152762.3(TSGA10IP):c.5G>A (p.Gly2Glu)	TSGA10IP (G2E)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2290000	NM_152762.3(TSGA10IP):c.119T>G (p.Leu40Arg)	TSGA10IP (L40R)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2477479	NM_152762.3(TSGA10IP):c.125C>T (p.Ser42Leu)	TSGA10IP (S42L)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2510875	NM_152762.3(TSGA10IP):c.128C>T (p.Thr43Ile)	TSGA10IP (T43I)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2603096	NM_152762.3(TSGA10IP):c.343A>T (p.Ile115Phe)	TSGA10IP (I115F)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GLikely benign
Select item 2533395	NM_152762.3(TSGA10IP):c.431G>A (p.Arg144His)	TSGA10IP (R144H +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2597327	NM_152762.3(TSGA10IP):c.442C>A (p.Arg148Ser)	TSGA10IP (R148S +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2298311	NM_152762.3(TSGA10IP):c.508A>C (p.Lys170Gln)	TSGA10IP (K34Q +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2282316	NM_152762.3(TSGA10IP):c.547A>G (p.Ile183Val)	TSGA10IP (I183V +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2245756	NM_152762.3(TSGA10IP):c.589G>T (p.Gly197Cys)	TSGA10IP (G61C +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2620436	NM_152762.3(TSGA10IP):c.607A>G (p.Arg203Gly)	TSGA10IP (R67G +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2293104	NM_152762.3(TSGA10IP):c.626C>T (p.Ser209Leu)	TSGA10IP (S209L +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2543697	NM_152762.3(TSGA10IP):c.848C>T (p.Ser283Phe)	TSGA10IP (S147F +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2559736	NM_152762.3(TSGA10IP):c.948G>C (p.Gln316His)	TSGA10IP (Q316H +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2236924	NM_152762.3(TSGA10IP):c.1035G>T (p.Arg345Ser)	TSGA10IP (R209S +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2227026	NM_152762.3(TSGA10IP):c.1058G>A (p.Arg353Gln)	TSGA10IP (R217Q +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2229443	NM_152762.3(TSGA10IP):c.1075G>A (p.Ala359Thr)	TSGA10IP (A64T +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2362558	NM_152762.3(TSGA10IP):c.1099G>A (p.Val367Met)	TSGA10IP (V367M +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2622559	NM_152762.3(TSGA10IP):c.1112T>C (p.Leu371Pro)	TSGA10IP (L371P +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2460178	NM_152762.3(TSGA10IP):c.1120C>T (p.Arg374Cys)	TSGA10IP (R374C +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2610523	NM_152762.3(TSGA10IP):c.1135C>G (p.Arg379Gly)	TSGA10IP (R243G +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2338622	NM_152762.3(TSGA10IP):c.1244T>G (p.Val415Gly)	TSGA10IP (V120G +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2246167	NM_152762.3(TSGA10IP):c.1273A>G (p.Arg425Gly)	TSGA10IP (R125G +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2484507	NM_152762.3(TSGA10IP):c.1432C>G (p.Arg478Gly)	TSGA10IP (R478G +4 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2532186	NM_152762.3(TSGA10IP):c.1613C>A (p.Thr538Asn)	TSGA10IP (T243N +4 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

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Items: 25