KRTAP13-2[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2523817	NM_181621.4(KRTAP13-2):c.520A>G (p.Thr174Ala)	KRTAP13-2 (T174A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407774	NM_181621.4(KRTAP13-2):c.461C>T (p.Ser154Phe)	KRTAP13-2 (S154F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116946	NM_181621.4(KRTAP13-2):c.422G>C (p.Gly141Ala)	KRTAP13-2 (G141A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116945	NM_181621.4(KRTAP13-2):c.421G>C (p.Gly141Arg)	KRTAP13-2 (G141R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617072	NM_181621.4(KRTAP13-2):c.403T>C (p.Cys135Arg)	KRTAP13-2 (C135R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116943	NM_181621.4(KRTAP13-2):c.355T>A (p.Ser119Thr)	KRTAP13-2 (S119T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289659	NM_181621.4(KRTAP13-2):c.325T>C (p.Ser109Pro)	KRTAP13-2 (S109P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460033	NM_181621.4(KRTAP13-2):c.323G>A (p.Arg108His)	KRTAP13-2 (R108H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116942	NM_181621.4(KRTAP13-2):c.322C>T (p.Arg108Cys)	KRTAP13-2 (R108C)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2310032	NM_181621.4(KRTAP13-2):c.244C>G (p.Arg82Gly)	KRTAP13-2 (R82G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116941	NM_181621.4(KRTAP13-2):c.227G>T (p.Cys76Phe)	KRTAP13-2 (C76F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359567	NM_181621.4(KRTAP13-2):c.203C>T (p.Thr68Met)	KRTAP13-2 (T68M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2622167	NM_181621.4(KRTAP13-2):c.101T>A (p.Leu34Gln)	KRTAP13-2 (L34Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457207	NM_181621.4(KRTAP13-2):c.92C>T (p.Pro31Leu)	KRTAP13-2 (P31L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546876	NM_181621.4(KRTAP13-2):c.58C>T (p.Arg20Cys)	KRTAP13-2 (R20C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289658	NM_181621.4(KRTAP13-2):c.50A>G (p.Asp17Gly)	KRTAP13-2 (D17G)	Single nucleotide variant (missense variant)	not specified	GLikely benign