"Ambry Genetics"[submitter] AND "KRTAP10-10"[gene] - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2607839	NM_181688.3(KRTAP10-10):c.23T>C (p.Ile8Thr)	KRTAP10-10, TSPEAR (I8T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2490386	NM_181688.3(KRTAP10-10):c.67C>T (p.Pro23Ser)	KRTAP10-10, TSPEAR (P23S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2480089	NM_181688.3(KRTAP10-10):c.91T>G (p.Cys31Gly)	KRTAP10-10, TSPEAR (C31G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2220886	NM_181688.3(KRTAP10-10):c.162G>T (p.Gln54His)	TSPEAR, KRTAP10-10 (Q54H)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2225255	NM_181688.3(KRTAP10-10):c.220T>C (p.Cys74Arg)	KRTAP10-10, TSPEAR (C74R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2344808	NM_181688.3(KRTAP10-10):c.520T>C (p.Cys174Arg)	KRTAP10-10, TSPEAR (C174R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2558953	NM_181688.3(KRTAP10-10):c.539C>T (p.Thr180Ile)	KRTAP10-10, TSPEAR (T180I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2373829	NM_181688.3(KRTAP10-10):c.568G>A (p.Val190Met)	KRTAP10-10, TSPEAR (V190M)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2354721	NM_181688.3(KRTAP10-10):c.605G>A (p.Cys202Tyr)	TSPEAR, KRTAP10-10 (C202Y)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2252354	NM_181688.3(KRTAP10-10):c.628G>A (p.Gly210Ser)	KRTAP10-10, TSPEAR (G210S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2546866	NM_181688.3(KRTAP10-10):c.634T>C (p.Ser212Pro)	KRTAP10-10, TSPEAR (S212P)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2356508	NM_181688.3(KRTAP10-10):c.665G>A (p.Arg222His)	TSPEAR, KRTAP10-10 (R222H)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2369268	NM_181688.3(KRTAP10-10):c.668C>T (p.Thr223Met)	KRTAP10-10, TSPEAR (T223M)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2325797	NM_181688.3(KRTAP10-10):c.695G>A (p.Arg232His)	KRTAP10-10, TSPEAR (R232H)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance