Related gene-specific medical variations for Gene (Select 386678) - ClinVar

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Items: 44

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3289611	NM_198692.3(KRTAP10-11):c.196G>A (p.Ala66Thr)	KRTAP10-11, TSPEAR (A66T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3289610	NM_198692.3(KRTAP10-11):c.701C>T (p.Ser234Phe)	KRTAP10-11, TSPEAR (S234F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3289609	NM_198692.3(KRTAP10-11):c.836G>A (p.Arg279His)	KRTAP10-11, TSPEAR (R279H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3289608	NM_198692.3(KRTAP10-11):c.459G>T (p.Lys153Asn)	KRTAP10-11, TSPEAR (K153N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3289607	NM_198692.3(KRTAP10-11):c.553C>A (p.Gln185Lys)	KRTAP10-11, TSPEAR (Q185K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116824	NM_198692.3(KRTAP10-11):c.89C>G (p.Pro30Arg)	KRTAP10-11, TSPEAR (P30R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116823	NM_198692.3(KRTAP10-11):c.854T>C (p.Leu285Pro)	KRTAP10-11, TSPEAR (L285P)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3116821	NM_198692.3(KRTAP10-11):c.463G>A (p.Val155Met)	KRTAP10-11, TSPEAR (V155M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116820	NM_198692.3(KRTAP10-11):c.343T>C (p.Cys115Arg)	KRTAP10-11, TSPEAR (C115R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116819	NM_198692.3(KRTAP10-11):c.193A>C (p.Ser65Arg)	KRTAP10-11, TSPEAR (S65R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116818	NM_198692.3(KRTAP10-11):c.154T>C (p.Cys52Arg)	KRTAP10-11, TSPEAR (C52R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116817	NM_198692.3(KRTAP10-11):c.131G>C (p.Ser44Thr)	KRTAP10-11, TSPEAR (S44T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3116816	NM_198692.3(KRTAP10-11):c.125C>G (p.Ser42Cys)	KRTAP10-11, TSPEAR (S42C)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2652778	NM_198692.3(KRTAP10-11):c.603C>T (p.Pro201=)	KRTAP10-11, TSPEAR	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2652777	NM_198692.3(KRTAP10-11):c.375G>A (p.Ser125=)	KRTAP10-11, TSPEAR	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2652776	NM_198692.3(KRTAP10-11):c.369T>C (p.Ala123=)	KRTAP10-11, TSPEAR	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2652775	NM_198692.3(KRTAP10-11):c.81T>C (p.Cys27=)	KRTAP10-11, TSPEAR	Single nucleotide variant (intron variant +1 more)	not provided	GLikely benign
Select item 2652774	NM_198692.3(KRTAP10-11):c.21T>C (p.Ser7=)	KRTAP10-11, TSPEAR	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2622512	NM_198692.3(KRTAP10-11):c.436T>G (p.Cys146Gly)	KRTAP10-11, TSPEAR (C146G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2602904	NM_198692.3(KRTAP10-11):c.757G>A (p.Val253Ile)	KRTAP10-11, TSPEAR (V253I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2595247	NM_198692.3(KRTAP10-11):c.772G>A (p.Ala258Thr)	KRTAP10-11, TSPEAR (A258T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2588017	NM_198692.3(KRTAP10-11):c.593A>G (p.Tyr198Cys)	KRTAP10-11, TSPEAR (Y198C)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2542434	NM_198692.3(KRTAP10-11):c.484T>C (p.Ser162Pro)	KRTAP10-11, TSPEAR (S162P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2533863	NM_198692.3(KRTAP10-11):c.346G>A (p.Val116Met)	KRTAP10-11, TSPEAR (V116M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2517492	NM_198692.3(KRTAP10-11):c.43G>A (p.Asp15Asn)	KRTAP10-11, TSPEAR (D15N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2514181	NM_198692.3(KRTAP10-11):c.793T>G (p.Ser265Ala)	KRTAP10-11, TSPEAR (S265A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2512601	NM_198692.3(KRTAP10-11):c.542C>A (p.Ser181Tyr)	KRTAP10-11, TSPEAR (S181Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2511566	NM_198692.3(KRTAP10-11):c.22G>A (p.Val8Ile)	KRTAP10-11, TSPEAR (V8I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2507915	NM_198692.3(KRTAP10-11):c.383G>A (p.Arg128Gln)	KRTAP10-11, TSPEAR (R128Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2494192	NM_198692.3(KRTAP10-11):c.473T>C (p.Val158Ala)	KRTAP10-11, TSPEAR (V158A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2487746	NM_198692.3(KRTAP10-11):c.353T>A (p.Val118Asp)	KRTAP10-11, TSPEAR (V118D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2475900	NM_198692.3(KRTAP10-11):c.16A>G (p.Met6Val)	KRTAP10-11, TSPEAR (M6V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2468617	NM_198692.3(KRTAP10-11):c.844A>T (p.Ser282Cys)	KRTAP10-11, TSPEAR (S282C)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2455625	NM_198692.3(KRTAP10-11):c.395G>T (p.Cys132Phe)	KRTAP10-11, TSPEAR (C132F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2404730	NM_198692.3(KRTAP10-11):c.272C>A (p.Thr91Asn)	KRTAP10-11, TSPEAR (T91N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2399916	NM_198692.3(KRTAP10-11):c.406T>A (p.Cys136Ser)	KRTAP10-11, TSPEAR (C136S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2343295	NM_198692.3(KRTAP10-11):c.865A>G (p.Ser289Gly)	KRTAP10-11, TSPEAR (S289G)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2343294	NM_198692.3(KRTAP10-11):c.863A>G (p.Tyr288Cys)	KRTAP10-11, TSPEAR (Y288C)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2335823	NM_198692.3(KRTAP10-11):c.692G>T (p.Cys231Phe)	KRTAP10-11, TSPEAR (C231F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2335204	NM_198692.3(KRTAP10-11):c.116C>T (p.Pro39Leu)	KRTAP10-11, TSPEAR (P39L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2242505	NM_198692.3(KRTAP10-11):c.613G>A (p.Val205Met)	KRTAP10-11, TSPEAR (V205M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2240445	NM_198692.3(KRTAP10-11):c.311G>A (p.Cys104Tyr)	KRTAP10-11, TSPEAR (C104Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2205803	NM_198692.3(KRTAP10-11):c.841G>A (p.Ala281Thr)	KRTAP10-11, TSPEAR (A281T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1801777	NM_198692.3(KRTAP10-11):c.112G>A (p.Ala38Thr)	KRTAP10-11, TSPEAR (A38T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign

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Links from Gene

Items: 44