Related gene-specific medical variations for Gene (Select 6895) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3324413	NM_134323.2(TARBP2):c.37G>A (p.Gly13Ser)	MAP3K12, TARBP2 (G13S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3173863	NM_134323.2(TARBP2):c.44G>A (p.Gly15Glu)	MAP3K12, TARBP2 (G15E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2598963	NM_134323.2(TARBP2):c.25G>A (p.Gly9Ser)	MAP3K12, TARBP2 (G9S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2396615	NM_134323.2(TARBP2):c.47T>C (p.Leu16Pro)	MAP3K12, TARBP2 (L16P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2379144	NM_134323.2(TARBP2):c.52A>G (p.Ser18Gly)	MAP3K12, TARBP2 (S18G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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