Related gene-specific medical variations for Gene (Select 283870) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3261763	NM_182563.4(BRICD5):c.682G>T (p.Asp228Tyr)	BRICD5, MLST8 (D228Y)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3261762	NM_182563.4(BRICD5):c.641C>T (p.Pro214Leu)	BRICD5, MLST8 (P214L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3135058	NM_182563.4(BRICD5):c.617A>C (p.Tyr206Ser)	BRICD5, MLST8 (Y206S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3135057	NM_182563.4(BRICD5):c.598C>G (p.Arg200Gly)	BRICD5, MLST8 (R200G)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2394719	NM_182563.4(BRICD5):c.625A>G (p.Ile209Val)	BRICD5, MLST8 (I209V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2323709	NM_182563.4(BRICD5):c.644G>A (p.Ser215Asn)	BRICD5, MLST8 (S215N)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2215915	NM_182563.4(BRICD5):c.607C>T (p.Arg203Trp)	BRICD5, MLST8 (R203W)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

ClinVar