Related gene-specific medical variations for Gene (Select 386683) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3289647	NM_198697.2(KRTAP12-3):c.232C>A (p.Pro78Thr)	KRTAP12-3, TSPEAR (P78T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3289646	NM_198697.2(KRTAP12-3):c.131T>C (p.Val44Ala)	KRTAP12-3, TSPEAR (V44A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116927	NM_198697.2(KRTAP12-3):c.112G>A (p.Val38Met)	TSPEAR, KRTAP12-3 (V38M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2610574	NM_198697.2(KRTAP12-3):c.34C>G (p.Pro12Ala)	KRTAP12-3, TSPEAR (P12A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2477634	NM_198697.2(KRTAP12-3):c.272G>A (p.Ser91Asn)	KRTAP12-3, TSPEAR (S91N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2456702	NM_198697.2(KRTAP12-3):c.41G>A (p.Cys14Tyr)	KRTAP12-3, TSPEAR (C14Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2394609	NM_198697.2(KRTAP12-3):c.100G>A (p.Val34Met)	KRTAP12-3, TSPEAR (V34M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2365672	NM_198697.2(KRTAP12-3):c.136G>A (p.Val46Met)	KRTAP12-3, TSPEAR (V46M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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