ClinVar Miner

List of variants in gene IDH2 reported as uncertain significance by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002168.4(IDH2):c.673G>A (p.Asp225Asn) rs142816010 0.00033
NM_002168.4(IDH2):c.1156G>C (p.Asp386His) rs774323865 0.00001
NM_002168.4(IDH2):c.265C>T (p.Arg89Cys) rs997901344 0.00001
NM_002168.4(IDH2):c.532C>T (p.Gln178Ter) rs763369478 0.00001
NM_002168.4(IDH2):c.662T>C (p.Met221Thr) rs376694064 0.00001
NM_002168.4(IDH2):c.1022C>T (p.Thr341Met)
NM_002168.4(IDH2):c.1076A>G (p.Gln359Arg)
NM_002168.4(IDH2):c.1272T>A (p.Asn424Lys)
NM_002168.4(IDH2):c.1285G>A (p.Glu429Lys) rs1900800432
NM_002168.4(IDH2):c.145C>G (p.Pro49Ala) rs1164126819
NM_002168.4(IDH2):c.394T>C (p.Trp132Arg)
NM_002168.4(IDH2):c.418C>T (p.Arg140Trp) rs267606870
NM_002168.4(IDH2):c.435dup (p.Thr146fs) rs747216375
NM_002168.4(IDH2):c.463A>C (p.Lys155Gln) rs2151549672
NM_002168.4(IDH2):c.695C>T (p.Ala232Val) rs1227626398
NM_002168.4(IDH2):c.715G>A (p.Ala239Thr) rs1596073614
NM_002168.4(IDH2):c.743T>G (p.Met248Arg) rs1418478547
NM_002168.4(IDH2):c.805A>G (p.Ile269Val) rs914590416
NM_002168.4(IDH2):c.823A>C (p.Lys275Gln) rs2505788493
NM_002168.4(IDH2):c.863G>T (p.Arg288Leu) rs2151548118
NM_002168.4(IDH2):c.913G>C (p.Val305Leu) rs138800371

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.