Related gene-specific medical variations for Gene (Select 5936) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3313190	NM_001198845.2(RBM14-RBM4):c.416G>A (p.Arg139Gln)	RBM14-RBM4, RBM4 (R164Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2641999	NM_001198846.2(RBM14-RBM4):c.338-2114C>T	RBM14-RBM4, RBM4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2385764	NM_001198844.2(RBM4):c.491T>C (p.Ile164Thr)	RBM4, RBM4B (I164T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2260483	NM_001198844.2(RBM4):c.467A>G (p.Tyr156Cys)	RBM4, RBM4B (Y156C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2211929	NM_001198845.2(RBM14-RBM4):c.637G>A (p.Ala213Thr)	RBM14-RBM4, RBM4 (A213T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1801730	NM_001198846.2(RBM14-RBM4):c.338-2091C>T	RBM14-RBM4, RBM4 (S275F +1 more)	Single nucleotide variant (missense variant +1 more)	Myoepithelial tumor	GUncertain significance

ClinVar