Related gene-specific medical variations for Gene (Select 22894) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3134767	NM_024808.5(BORA):c.1672A>G (p.Ser558Gly)	BORA, DIS3 (S558G +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2489778	NM_024808.5(BORA):c.1576T>C (p.Cys526Arg)	BORA, DIS3 (C526R +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2481471	NM_024808.5(BORA):c.1664A>T (p.Gln555Leu)	BORA, DIS3 (Q504L +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2454762	NM_024808.5(BORA):c.1675C>A (p.Pro559Thr)	BORA, DIS3 (P559T +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2324117	NM_024808.5(BORA):c.1579G>C (p.Glu527Gln)	BORA, DIS3 (E457Q +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2221012	NM_024808.5(BORA):c.1658C>T (p.Pro553Leu)	BORA, DIS3 (P483L +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance

ClinVar