Related gene-specific medical variations for Gene (Select 140707) - ClinVar

Format

Sort by

Choose Destination

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3261760	NM_080626.6(BRI3BP):c.4G>C (p.Gly2Arg)	BRI3BP, LOC130009167 (G2R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541696	NM_080626.6(BRI3BP):c.28C>G (p.Leu10Val)	BRI3BP, LOC130009168 (L10V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402548	NM_080626.6(BRI3BP):c.194A>G (p.Asn65Ser)	BRI3BP, LOC130009169 (N65S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

Format

Sort by

Choose Destination

ClinVar