Related gene-specific medical variations for Gene (Select 386674) - ClinVar

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Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3116883	NM_198688.3(KRTAP10-6):c.678G>C (p.Gln226His)	KRTAP10-6, TSPEAR (Q226H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116882	NM_198688.3(KRTAP10-6):c.599G>A (p.Cys200Tyr)	KRTAP10-6, TSPEAR (C200Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116880	NM_198688.3(KRTAP10-6):c.469G>A (p.Val157Met)	KRTAP10-6, TSPEAR (V157M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116879	NM_198688.3(KRTAP10-6):c.154T>C (p.Cys52Arg)	KRTAP10-6, TSPEAR (C52R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116878	NM_198688.3(KRTAP10-6):c.142G>A (p.Ala48Thr)	KRTAP10-6, TSPEAR (A48T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2652768	NM_198688.3(KRTAP10-6):c.331G>A (p.Val111Met)	KRTAP10-6, TSPEAR (V111M)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2578916	NM_198688.3(KRTAP10-6):c.371G>A (p.Cys124Tyr)	KRTAP10-6, TSPEAR (C124Y)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2553990	NM_198688.3(KRTAP10-6):c.1037G>A (p.Arg346His)	KRTAP10-6, TSPEAR (R346H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2545213	NM_198688.3(KRTAP10-6):c.112C>T (p.Pro38Ser)	KRTAP10-6, TSPEAR (P38S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2544079	NM_198688.3(KRTAP10-6):c.1021G>C (p.Val341Leu)	KRTAP10-6, TSPEAR (V341L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2541462	NM_198688.3(KRTAP10-6):c.820G>A (p.Val274Ile)	KRTAP10-6, TSPEAR (V274I)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2512911	NM_198688.3(KRTAP10-6):c.740C>T (p.Ser247Phe)	TSPEAR, KRTAP10-6 (S247F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2455751	NM_198688.3(KRTAP10-6):c.105C>A (p.Asp35Glu)	KRTAP10-6, TSPEAR (D35E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2379533	NM_198688.3(KRTAP10-6):c.566C>T (p.Ala189Val)	KRTAP10-6, TSPEAR (A189V)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2363512	NM_198688.3(KRTAP10-6):c.17T>C (p.Met6Thr)	KRTAP10-6, TSPEAR (M6T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2363073	NM_198688.3(KRTAP10-6):c.1036C>T (p.Arg346Cys)	KRTAP10-6, TSPEAR (R346C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2355036	NM_198688.3(KRTAP10-6):c.134C>T (p.Pro45Leu)	KRTAP10-6, TSPEAR (P45L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2336046	NM_198688.3(KRTAP10-6):c.397T>A (p.Ser133Thr)	KRTAP10-6, TSPEAR (S133T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2301231	NM_198688.3(KRTAP10-6):c.583C>G (p.Pro195Ala)	KRTAP10-6, TSPEAR (P195A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2266091	NM_198688.3(KRTAP10-6):c.671G>A (p.Cys224Tyr)	KRTAP10-6, TSPEAR (C224Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2262511	NM_198688.3(KRTAP10-6):c.360C>G (p.Cys120Trp)	KRTAP10-6, TSPEAR (C120W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 235482	NM_198688.3(KRTAP10-6):c.107A>C (p.Asp36Ala)	KRTAP10-6, TSPEAR (D36A)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign

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Items: 22