Related gene-specific medical variations for Gene (Select 7189) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3181790	NM_004620.4(TRAF6):c.233G>A (p.Arg78Gln)	LOC126861190, TRAF6 (R78Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549644	NM_004620.4(TRAF6):c.59G>A (p.Cys20Tyr)	LOC126861190, TRAF6 (C20Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243529	NM_004620.4(TRAF6):c.131A>G (p.Asn44Ser)	LOC126861190, TRAF6 (N44S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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