ClinVar Miner

List of variants in gene RBM45 reported as uncertain significance

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_152945.4(RBM45):c.932C>T (p.Pro311Leu) rs574520764 0.00004
NM_152945.4(RBM45):c.739C>T (p.Arg247Cys) rs755298569 0.00003
NM_152945.4(RBM45):c.1041G>C (p.Trp347Cys) rs570468892 0.00002
NM_152945.4(RBM45):c.281A>C (p.Asn94Thr) rs764322049 0.00002
NM_152945.4(RBM45):c.548G>A (p.Arg183Gln) rs139412077 0.00002
NM_152945.4(RBM45):c.1151C>G (p.Ala384Gly) rs1473237490 0.00001
NM_152945.4(RBM45):c.944T>C (p.Ile315Thr) rs372335848 0.00001
NM_152945.4(RBM45):c.945A>G (p.Ile315Met) rs146621378 0.00001
NM_152945.4(RBM45):c.109C>T (p.Pro37Ser)
NM_152945.4(RBM45):c.1227A>G (p.Ile409Met)
NM_152945.4(RBM45):c.1235G>A (p.Arg412His)
NM_152945.4(RBM45):c.1300G>A (p.Asp434Asn)
NM_152945.4(RBM45):c.1313C>G (p.Ala438Gly)
NM_152945.4(RBM45):c.1337A>G (p.His446Arg) rs1474216702
NM_152945.4(RBM45):c.206C>G (p.Ala69Gly)
NM_152945.4(RBM45):c.801A>G (p.Ile267Met) rs2468390029
NM_152945.4(RBM45):c.892A>T (p.Ile298Phe) rs115290266
NM_152945.4(RBM45):c.965A>T (p.Asp322Val)
NM_152945.4(RBM45):c.977C>T (p.Ala326Val)
NM_152945.4(RBM45):c.997A>G (p.Met333Val)

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.