ClinVar Miner

List of variants in gene combination LOC129390903, RAD51C reported as likely benign for Fanconi anemia complementation group O

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 31
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_058216.3(RAD51C):c.705+14T>C rs771168730 0.00003
NM_058216.3(RAD51C):c.705+10A>G rs377586976 0.00002
NM_058216.3(RAD51C):c.651A>G (p.Thr217=) rs757915374 0.00001
NM_058216.3(RAD51C):c.654G>A (p.Glu218=) rs1388636466 0.00001
NM_058216.3(RAD51C):c.615T>C (p.Leu205=) rs2143797988
NM_058216.3(RAD51C):c.636C>T (p.Arg212=) rs1481957875
NM_058216.3(RAD51C):c.639T>C (p.Cys213=) rs2143798905
NM_058216.3(RAD51C):c.645C>T (p.Asp215=) rs2143799278
NM_058216.3(RAD51C):c.648C>T (p.Tyr216=) rs750060665
NM_058216.3(RAD51C):c.651A>C (p.Thr217=) rs757915374
NM_058216.3(RAD51C):c.651A>T (p.Thr217=) rs757915374
NM_058216.3(RAD51C):c.657A>G (p.Leu219=) rs2143800069
NM_058216.3(RAD51C):c.658C>T (p.Leu220=) rs1555597205
NM_058216.3(RAD51C):c.663A>C (p.Ala221=) rs2048273669
NM_058216.3(RAD51C):c.666A>G (p.Gln222=) rs1567794382
NM_058216.3(RAD51C):c.669T>C (p.Val223=) rs2143800599
NM_058216.3(RAD51C):c.672_705+65dup rs1555597214
NM_058216.3(RAD51C):c.681A>C (p.Pro227=) rs1177043110
NM_058216.3(RAD51C):c.681A>G (p.Pro227=) rs1177043110
NM_058216.3(RAD51C):c.687C>T (p.Phe229=) rs780177888
NM_058216.3(RAD51C):c.690T>C (p.Leu230=) rs2143801640
NM_058216.3(RAD51C):c.693A>G (p.Ser231=) rs1598473581
NM_058216.3(RAD51C):c.696A>G (p.Glu232=) rs786201177
NM_058216.3(RAD51C):c.702A>C (p.Ser234=) rs2143802342
NM_058216.3(RAD51C):c.702A>G (p.Ser234=) rs2143802342
NM_058216.3(RAD51C):c.705+13C>A rs1460412844
NM_058216.3(RAD51C):c.705+13C>T rs1460412844
NM_058216.3(RAD51C):c.705+15A>G rs2143802858
NM_058216.3(RAD51C):c.705+16C>G rs2143802894
NM_058216.3(RAD51C):c.705+9C>G rs1598473685
NM_058216.3(RAD51C):c.705+9C>T rs1598473685

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.