Related gene-specific medical variations for Gene (Select 386676) - ClinVar

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Items: 41

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3289641	NM_198690.3(KRTAP10-9):c.23T>C (p.Ile8Thr)	KRTAP10-9, TSPEAR (I8T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3289640	NM_198690.3(KRTAP10-9):c.713T>C (p.Val238Ala)	KRTAP10-9, TSPEAR (V238A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3289639	NM_198690.3(KRTAP10-9):c.411G>C (p.Gln137His)	KRTAP10-9, TSPEAR (Q137H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3289638	NM_198690.3(KRTAP10-9):c.637T>C (p.Ser213Pro)	KRTAP10-9, TSPEAR (S213P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3289637	NM_198690.3(KRTAP10-9):c.131C>G (p.Thr44Ser)	KRTAP10-9, TSPEAR (T44S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3289636	NM_198690.3(KRTAP10-9):c.125G>C (p.Cys42Ser)	KRTAP10-9, TSPEAR (C42S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3289635	NM_198690.3(KRTAP10-9):c.85C>T (p.Pro29Ser)	KRTAP10-9, TSPEAR (P29S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3289634	NM_198690.3(KRTAP10-9):c.7G>A (p.Ala3Thr)	KRTAP10-9, TSPEAR (A3T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3289633	NM_198690.3(KRTAP10-9):c.154C>T (p.Arg52Cys)	KRTAP10-9, TSPEAR (R52C)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3116913	NM_198690.3(KRTAP10-9):c.88C>T (p.Pro30Ser)	KRTAP10-9, TSPEAR (P30S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116912	NM_198690.3(KRTAP10-9):c.863A>G (p.Gln288Arg)	KRTAP10-9, TSPEAR (Q288R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116911	NM_198690.3(KRTAP10-9):c.784T>C (p.Cys262Arg)	KRTAP10-9, TSPEAR (C262R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116910	NM_198690.3(KRTAP10-9):c.719G>A (p.Arg240Lys)	KRTAP10-9, TSPEAR (R240K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116908	NM_198690.3(KRTAP10-9):c.337G>A (p.Val113Ile)	KRTAP10-9, TSPEAR (V113I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116907	NM_198690.3(KRTAP10-9):c.307G>A (p.Val103Ile)	KRTAP10-9, TSPEAR (V103I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116906	NM_198690.3(KRTAP10-9):c.283T>G (p.Cys95Gly)	KRTAP10-9, TSPEAR (C95G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116905	NM_198690.3(KRTAP10-9):c.151A>T (p.Ser51Cys)	KRTAP10-9, TSPEAR (S51C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116904	NM_198690.3(KRTAP10-9):c.131C>A (p.Thr44Asn)	KRTAP10-9, TSPEAR (T44N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2652773	NM_198690.3(KRTAP10-9):c.759C>T (p.Pro253=)	KRTAP10-9, TSPEAR	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2652772	NM_198690.3(KRTAP10-9):c.72G>A (p.Glu24=)	KRTAP10-9, TSPEAR	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2621062	NM_198690.3(KRTAP10-9):c.94T>G (p.Cys32Gly)	KRTAP10-9, TSPEAR (C32G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2621061	NM_198690.3(KRTAP10-9):c.86C>T (p.Pro29Leu)	KRTAP10-9, TSPEAR (P29L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2620464	NM_198690.3(KRTAP10-9):c.448T>C (p.Cys150Arg)	KRTAP10-9, TSPEAR (C150R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2591170	NM_198690.3(KRTAP10-9):c.227C>T (p.Thr76Met)	KRTAP10-9, TSPEAR (T76M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2538776	NM_198690.3(KRTAP10-9):c.97G>A (p.Ala33Thr)	KRTAP10-9, TSPEAR (A33T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2492505	NM_198690.3(KRTAP10-9):c.739G>C (p.Val247Leu)	KRTAP10-9, TSPEAR (V247L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2460118	NM_198690.3(KRTAP10-9):c.85C>A (p.Pro29Thr)	KRTAP10-9, TSPEAR (P29T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2456883	NM_198690.3(KRTAP10-9):c.733G>A (p.Val245Met)	KRTAP10-9, TSPEAR (V245M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2397155	NM_198690.3(KRTAP10-9):c.404C>T (p.Ser135Phe)	KRTAP10-9, TSPEAR (S135F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2389522	NM_198690.3(KRTAP10-9):c.697C>T (p.Leu233Phe)	KRTAP10-9, TSPEAR (L233F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2379090	NM_198690.3(KRTAP10-9):c.337G>C (p.Val113Leu)	KRTAP10-9, TSPEAR (V113L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2356943	NM_198690.3(KRTAP10-9):c.112G>A (p.Ala38Thr)	KRTAP10-9, TSPEAR (A38T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2352457	NM_198690.3(KRTAP10-9):c.760A>G (p.Thr254Ala)	KRTAP10-9, TSPEAR (T254A)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2350609	NM_198690.3(KRTAP10-9):c.301G>A (p.Val101Met)	KRTAP10-9, TSPEAR (V101M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2332784	NM_198690.3(KRTAP10-9):c.826T>A (p.Cys276Ser)	KRTAP10-9, TSPEAR (C276S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2320831	NM_198690.3(KRTAP10-9):c.854C>G (p.Ser285Cys)	KRTAP10-9, TSPEAR (S285C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2320830	NM_198690.3(KRTAP10-9):c.850T>C (p.Phe284Leu)	KRTAP10-9, TSPEAR (F284L)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2311446	NM_198690.3(KRTAP10-9):c.17T>C (p.Met6Thr)	KRTAP10-9, TSPEAR (M6T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2307065	NM_198690.3(KRTAP10-9):c.233C>T (p.Ser78Leu)	KRTAP10-9, TSPEAR (S78L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2304807	NM_198690.3(KRTAP10-9):c.503G>T (p.Cys168Phe)	KRTAP10-9, TSPEAR (C168F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2281182	NM_198690.3(KRTAP10-9):c.89C>T (p.Pro30Leu)	KRTAP10-9, TSPEAR (P30L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Links from Gene

Items: 41