ClinVar Miner

List of variants in gene combination RAD50, TH2LCRR reported as likely benign for Hereditary cancer-predisposing syndrome

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 42
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_005732.4(RAD50):c.3879C>T (p.Ile1293=) rs28903094 0.00293
NM_005732.4(RAD50):c.3861C>T (p.Tyr1287=) rs368356436 0.00019
NM_005732.4(RAD50):c.3790C>T (p.Leu1264Phe) rs199579239 0.00009
NM_005732.4(RAD50):c.3807T>C (p.His1269=) rs755777007 0.00001
NM_005732.4(RAD50):c.3813A>G (p.Glu1271=) rs1302002047 0.00001
NM_005732.4(RAD50):c.3876C>T (p.Asn1292=) rs1300783013 0.00001
NM_005732.4(RAD50):c.3897T>A (p.Ile1299=) rs767384027 0.00001
NM_005732.4(RAD50):c.3902A>G (p.Lys1301Arg) rs201766077 0.00001
NM_005732.4(RAD50):c.3915C>T (p.Ser1305=) rs1183659259 0.00001
NM_005732.4(RAD50):c.3930T>C (p.Asn1310=) rs878854803 0.00001
NM_005732.4(RAD50):c.3774G>A (p.Gln1258=) rs1060504404
NM_005732.4(RAD50):c.3777G>A (p.Gln1259=) rs587780157
NM_005732.4(RAD50):c.3783C>T (p.Asn1261=) rs1581024957
NM_005732.4(RAD50):c.3786C>T (p.Phe1262=) rs267600344
NM_005732.4(RAD50):c.3789G>A (p.Gln1263=) rs115706334
NM_005732.4(RAD50):c.3792T>A (p.Leu1264=) rs2149866888
NM_005732.4(RAD50):c.3798A>G (p.Val1266=)
NM_005732.4(RAD50):c.3801C>T (p.Ile1267=) rs1554101325
NM_005732.4(RAD50):c.3810T>C (p.Asp1270=) rs1486093198
NM_005732.4(RAD50):c.3834A>G (p.Gly1278=)
NM_005732.4(RAD50):c.3840T>C (p.Ser1280=)
NM_005732.4(RAD50):c.3843A>G (p.Glu1281=) rs1581025084
NM_005732.4(RAD50):c.3849G>A (p.Val1283=) rs1160803447
NM_005732.4(RAD50):c.3855A>G (p.Lys1285=) rs1581025096
NM_005732.4(RAD50):c.3858C>T (p.Phe1286=) rs1581025102
NM_005732.4(RAD50):c.3862A>C (p.Arg1288=)
NM_005732.4(RAD50):c.3873G>A (p.Lys1291=) rs2149867004
NM_005732.4(RAD50):c.3877_3879dup (p.Ile1293dup) rs765370709
NM_005732.4(RAD50):c.3888C>T (p.Cys1296=) rs1581025172
NM_005732.4(RAD50):c.3891A>C (p.Ser1297=) rs2149867053
NM_005732.4(RAD50):c.3891A>G (p.Ser1297=) rs2149867053
NM_005732.4(RAD50):c.3894G>A (p.Glu1298=) rs1751745380
NM_005732.4(RAD50):c.3897T>C (p.Ile1299=) rs767384027
NM_005732.4(RAD50):c.3900G>A (p.Val1300=) rs2149867065
NM_005732.4(RAD50):c.3906C>T (p.Cys1302=) rs2149867072
NM_005732.4(RAD50):c.3908G>A (p.Ser1303Asn) rs766044158
NM_005732.4(RAD50):c.3909T>C (p.Ser1303=) rs2149867080
NM_005732.4(RAD50):c.3912T>C (p.Val1304=)
NM_005732.4(RAD50):c.3918C>G (p.Ser1306=) rs1554101337
NM_005732.4(RAD50):c.3921G>C (p.Leu1307=) rs1554101338
NM_005732.4(RAD50):c.3933T>C (p.Val1311=) rs876660513
NM_005732.4(RAD50):c.3938_*30dup (p.Ter1313=) rs2149867108

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.