Related gene-specific medical variations for Gene (Select 22795) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2381541	NM_007361.4(NID2):c.4108T>C (p.Cys1370Arg)	NID2, RTRAF (C1370R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2318526	NM_007361.4(NID2):c.3741C>G (p.Asp1247Glu)	NID2, RTRAF (D1247E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2288186	NM_007361.4(NID2):c.4051G>C (p.Glu1351Gln)	NID2, RTRAF (E1351Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2267028	NM_007361.4(NID2):c.4070G>C (p.Arg1357Pro)	NID2, RTRAF (R1357P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2223887	NM_007361.4(NID2):c.3778T>G (p.Leu1260Val)	NID2, RTRAF (L1260V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 724770	NM_007361.4(NID2):c.3979C>T (p.His1327Tyr)	NID2, RTRAF (H1327Y)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign

ClinVar