ClinVar Miner

List of variants in gene XRCC2 reported by Sema4, Sema4

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_005431.2(XRCC2):c.808T>G (p.Phe270Val) rs145085742 0.00205
NM_005431.2(XRCC2):c.283A>G (p.Ile95Val) rs140214637 0.00016
NM_005431.2(XRCC2):c.678T>C (p.Tyr226=) rs143357617 0.00010
NM_005431.2(XRCC2):c.477C>T (p.Arg159=) rs202226401 0.00008
NM_005431.2(XRCC2):c.115G>A (p.Val39Met) rs730882040 0.00005
NM_005431.2(XRCC2):c.476G>A (p.Arg159His) rs367696886 0.00005
NM_005431.2(XRCC2):c.450C>G (p.Ser150Arg) rs371453207 0.00004
NM_005431.2(XRCC2):c.501C>A (p.Asn167Lys) rs149929851 0.00004
NM_005431.2(XRCC2):c.562C>T (p.Arg188Cys) rs139219364 0.00004
NM_005431.2(XRCC2):c.773G>A (p.Arg258His) rs149186933 0.00004
NM_005431.2(XRCC2):c.190C>T (p.Arg64Ter) rs151110146 0.00003
NM_005431.2(XRCC2):c.596T>C (p.Met199Thr) rs149099078 0.00002
NM_005431.2(XRCC2):c.238T>C (p.Phe80Leu) rs751980448 0.00001
NM_005431.2(XRCC2):c.356A>C (p.Tyr119Ser) rs540634835 0.00001
NM_005431.2(XRCC2):c.746G>C (p.Ser249Thr) rs781507499 0.00001
NM_005431.2(XRCC2):c.236T>C (p.Leu79Ser) rs1777615098
NM_005431.2(XRCC2):c.353T>G (p.Val118Gly) rs185815454
NM_005431.2(XRCC2):c.375C>G (p.His125Gln) rs2116987965
NM_005431.2(XRCC2):c.795A>T (p.Leu265Phe) rs1159235024
NM_005431.2(XRCC2):c.810dup (p.Ile271fs) rs730882049
NM_005431.2(XRCC2):c.825T>C (p.Ser275=) rs770438650

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.