ClinVar Miner

List of variants in gene RBM15 reported by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 34
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_022768.5(RBM15):c.472T>G (p.Ser158Ala) rs200933258 0.00023
NM_022768.5(RBM15):c.803C>T (p.Pro268Leu) rs139719642 0.00009
NM_022768.5(RBM15):c.990A>C (p.Glu330Asp) rs763275756 0.00005
NM_022768.5(RBM15):c.799C>T (p.Pro267Ser) rs200277475 0.00003
NM_022768.5(RBM15):c.1312A>G (p.Ile438Val) rs1166283363 0.00001
NM_022768.5(RBM15):c.1355C>T (p.Thr452Ile) rs1179366059 0.00001
NM_022768.5(RBM15):c.1697A>G (p.Asp566Gly) rs758837325 0.00001
NM_022768.5(RBM15):c.1765C>T (p.Pro589Ser) rs761567136 0.00001
NM_022768.5(RBM15):c.426C>G (p.Ser142Arg) rs781645412 0.00001
NM_022768.5(RBM15):c.458C>T (p.Ser153Phe) rs1271095060 0.00001
NM_022768.5(RBM15):c.844C>T (p.His282Tyr) rs768296558 0.00001
NM_022768.5(RBM15):c.1007A>G (p.Tyr336Cys)
NM_022768.5(RBM15):c.1063G>A (p.Ala355Thr)
NM_022768.5(RBM15):c.1069C>T (p.Pro357Ser) rs139024479
NM_022768.5(RBM15):c.1163G>T (p.Ser388Ile)
NM_022768.5(RBM15):c.1454A>G (p.Asp485Gly)
NM_022768.5(RBM15):c.1523C>T (p.Thr508Ile)
NM_022768.5(RBM15):c.1526A>G (p.His509Arg)
NM_022768.5(RBM15):c.1642C>G (p.Leu548Val)
NM_022768.5(RBM15):c.1738C>G (p.Leu580Val) rs2523875040
NM_022768.5(RBM15):c.1757G>T (p.Trp586Leu)
NM_022768.5(RBM15):c.1775C>T (p.Pro592Leu) rs773151139
NM_022768.5(RBM15):c.1781G>A (p.Arg594Gln)
NM_022768.5(RBM15):c.2373G>T (p.Met791Ile) rs767879552
NM_022768.5(RBM15):c.2374C>A (p.Leu792Ile)
NM_022768.5(RBM15):c.2474A>C (p.Lys825Thr) rs375892527
NM_022768.5(RBM15):c.2552T>C (p.Val851Ala) rs2523881465
NM_022768.5(RBM15):c.2602G>A (p.Asp868Asn)
NM_022768.5(RBM15):c.395A>G (p.Lys132Arg)
NM_022768.5(RBM15):c.617A>G (p.His206Arg)
NM_022768.5(RBM15):c.619C>G (p.Leu207Val)
NM_022768.5(RBM15):c.709C>T (p.Arg237Cys) rs1384760735
NM_022768.5(RBM15):c.763C>T (p.Arg255Cys) rs768241522
NM_022768.5(RBM15):c.977A>G (p.Asp326Gly)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.