Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.152648840_152648849delCA579080840XRCC2c.470_479del (p.Ser157CysfsTer6)
c.638_647del (p.Ser213CysfsTer6)
n.660_669del
 dbSNP gnomAD v2 gnomAD v4
7g.152648848_152648849delCA1753246908XRCC2c.471_472del (p.Arg158ThrfsTer4)
c.639_640del (p.Arg214ThrfsTer4)
n.661_662del
 dbSNP
7g.152648848A>CCA370198271XRCC2c.469T>G (p.Ser157Ala)
c.637T>G (p.Ser213Ala)
n.659T>G
7g.152648848A>GCA370198270XRCC2c.469T>C (p.Ser157Pro)
c.637T>C (p.Ser213Pro)
n.659T>C
 ClinVar gnomAD v4
7g.152648848A>TCA370198269XRCC2c.469T>A (p.Ser157Thr)
c.637T>A (p.Ser213Thr)
n.659T>A
7g.152648849G>ACA458895353XRCC2c.468C>T (p.Ala156=)
c.636C>T (p.Ala212=)
n.658C>T
 ClinVar dbSNP
7g.152648849G>CCA169486944XRCC2c.468C>G (p.Ala156=)
c.636C>G (p.Ala212=)
n.658C>G
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.152648849G=CA1753246913XRCC2c.468C= (p.Ala156=)
c.636C= (p.Ala212=)
n.658C=
7g.152648849G>TCA458895354XRCC2c.468C>A (p.Ala156=)
c.636C>A (p.Ala212=)
n.658C>A
7g.152648850G>ACA370198272XRCC2c.467C>T (p.Ala156Val)
c.635C>T (p.Ala212Val)
n.657C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.152648850G>CCA370198273XRCC2c.467C>G (p.Ala156Gly)
c.635C>G (p.Ala212Gly)
n.657C>G
7g.152648850G=CA1753246916XRCC2c.467C= (p.Ala156=)
c.635C= (p.Ala212=)
n.657C=
7g.152648850G>TCA4582317XRCC2c.467C>A (p.Ala156Asp)
c.635C>A (p.Ala212Asp)
n.657C>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648851C>ACA370198274XRCC2c.466G>T (p.Ala156Ser)
c.634G>T (p.Ala212Ser)
n.656G>T
 dbSNP
7g.152648851C=CA1753246918XRCC2c.466G= (p.Ala156=)
c.634G= (p.Ala212=)
n.656G=
7g.152648851C>GCA370198275XRCC2c.466G>C (p.Ala156Pro)
c.634G>C (p.Ala212Pro)
n.656G>C
7g.152648851C>TCA370198276XRCC2c.466G>A (p.Ala156Thr)
c.634G>A (p.Ala212Thr)
n.656G>A
 dbSNP gnomAD v4
7g.152648852A>CCA370198277XRCC2c.465T>G (p.His155Gln)
c.633T>G (p.His211Gln)
n.655T>G
7g.152648852A>GCA458895356XRCC2c.465T>C (p.His155=)
c.633T>C (p.His211=)
n.655T>C
 ClinVar dbSNP
7g.152648852A>TCA370198278XRCC2c.465T>A (p.His155Gln)
c.633T>A (p.His211Gln)
n.655T>A
7g.152648853T>ACA370198279XRCC2c.464A>T (p.His155Leu)
c.632A>T (p.His211Leu)
n.654A>T
 dbSNP
7g.152648853T>CCA370198280XRCC2c.464A>G (p.His155Arg)
c.632A>G (p.His211Arg)
n.654A>G
7g.152648853T>GCA370198281XRCC2c.464A>C (p.His155Pro)
c.632A>C (p.His211Pro)
n.654A>C
 dbSNP
7g.152648853T=CA1753246921XRCC2c.464A= (p.His155=)
c.632A= (p.His211=)
n.654A=
7g.152648854G>ACA370198284XRCC2c.463C>T (p.His155Tyr)
c.631C>T (p.His211Tyr)
n.653C>T
 ClinVar dbSNP gnomAD v4
7g.152648854G>CCA370198282XRCC2c.463C>G (p.His155Asp)
c.631C>G (p.His211Asp)
n.653C>G
 ClinVar
7g.152648854G>TCA370198283XRCC2c.463C>A (p.His155Asn)
c.631C>A (p.His211Asn)
n.653C>A
7g.152648855A>CCA458895360XRCC2c.462T>G (p.Ser154=)
c.630T>G (p.Ser210=)
n.652T>G
7g.152648855A>GCA458895361XRCC2c.462T>C (p.Ser154=)
c.630T>C (p.Ser210=)
n.652T>C
7g.152648855A>TCA458895362XRCC2c.462T>A (p.Ser154=)
c.630T>A (p.Ser210=)
n.652T>A
7g.152648856G>ACA370198285XRCC2c.461C>T (p.Ser154Phe)
c.629C>T (p.Ser210Phe)
n.651C>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.152648856G>CCA370198286XRCC2c.461C>G (p.Ser154Cys)
c.629C>G (p.Ser210Cys)
n.651C>G
7g.152648856G=CA1753246923XRCC2c.461C= (p.Ser154=)
c.629C= (p.Ser210=)
n.651C=
7g.152648856G>TCA370198287XRCC2c.461C>A (p.Ser154Tyr)
c.629C>A (p.Ser210Tyr)
n.651C>A
7g.152648857A=CA1753246927XRCC2c.460T= (p.Ser154=)
c.628T= (p.Ser210=)
n.650T=
7g.152648857A>CCA370198288XRCC2c.460T>G (p.Ser154Ala)
c.628T>G (p.Ser210Ala)
n.650T>G
7g.152648857A>GCA370198289XRCC2c.460T>C (p.Ser154Pro)
c.628T>C (p.Ser210Pro)
n.650T>C
 ClinVar dbSNP
7g.152648857A>TCA370198290XRCC2c.460T>A (p.Ser154Thr)
c.628T>A (p.Ser210Thr)
n.650T>A
7g.152648858A>CCA458895365XRCC2c.459T>G (p.Pro153=)
c.627T>G (p.Pro209=)
n.649T>G
7g.152648858A>GCA458895366XRCC2c.459T>C (p.Pro153=)
c.627T>C (p.Pro209=)
n.649T>C
 ClinVar
7g.152648858A>TCA458895367XRCC2c.459T>A (p.Pro153=)
c.627T>A (p.Pro209=)
n.649T>A
7g.152648858_152651262delinsGGTTTGTTGATAATAATAAGAAAGGCCAGGTGCGGTGGTTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTAGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGCAAAACCCCATCTCTACCAAAAATACAAAAATTAGCTGGGCGCGGTAGCGCACGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCGAAAGTTGCAGTAAGCCAAGATTGAACCACTGCACTCCAGCCTAGGCAACAGAACAAGACTCCATCTCAAAAAAAAATTAAAATTAAATAATAAGAAATAAAGTAATTGCATTTTTTTGTGTTTTTGTTTTTGTTTTTTGAGACGGAGTTTCGCTCTTGTCGCCCAGGCTGGAGTCCAATGGCGTGATCTCAGCTCACTGCAACCTCTGTCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCTCAAGTAGCTGGGATTACAGGTGCCCACCACCATGCCCAGCTAATTTTTTGTATTTTTAGTAGGGTTTCAGTATGTTGGCCAGGCTGGTCTTGAATTCCTGACCTCAGGTGATCCTCCCGCCTCTGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGCCCAGCCCTTGAATCCGTATTTAGACCATCATTTGGTTGGGGCTAATAATTGGCATTTTAACATAGTGTTTCCAATCAGGTAGTTCAGCCGTAAATTAATAATGACAAGCAAGAGTTGAATGCCACTGTGAGTGCATTTTGAAAAGCTCTGGAAGCAAGGCAACTTCCCCAGTGTTGTTTGATTTAACTTGTGCTGTCCTTAGTTATTCGAGCCTAGATAGAAGGAGAGTTGGAGTCTTTAACGTTCAGAGTAGTTGACTTTGATTTTTAATGCTAGGAAAATAATTTCTAATGCAGCTGGACATGGTTTCCAGAGATAATTCAAATAGCAAAGAATAACTGAAGGCAGTTTGGGAACGTGTAAGGTTGTTTTCAGTTGAAGGATGCTGTTGGCATTTAGGGTCTGAGAGCCATGGGCTCTTGCCTCAATAATGTGTGAAACCACAAAATCCAGAATTGTTCCCCCCATAACATCAATAACACTGAGAAACCTAATTAGGGAGTGCCTTCACCTGCGTGTCATAGAAGTCCAACTTAGTGGCTTGCCCAGGTGGAGGCTTGTTTTCCTCACATCCTGAGTGGCACAGAGGCAGGCTGTGCGTGGCTGGTGGGGGCTCCGTGTGCCCAGAGTCCTGGGTACCTTCTGTCTTCCACGCCACCATCCTAAGGGTGGGTTTCATCCTCACTGCTTCCAGATGGCTGCTCCACCCCCACAGGAGGGTGCGGCAGGGCAGAAGGGGTCCCTGGATAGGAAAGAATCATCAACAGAGAGCAGCCTGCATCTCACTGGCGACAGCTGTGTTACCTGGTAACCTTGCTTTTCAAAGGAGACTATGAAAAATAGTTTTAAAGTGGACACATTTCCCTCCCCATCAAATTGGGTTTTATACTTTAGGAAGAAGGGAAGAATGGATATAGTGTAATCAACTACCAGAAAGGGTGTGTACTGTAGTCATCAGATTTTGGAAAGGCCCTAGATCTGTGGCTCTTTATTTTTGAATCTTACAAATTGAAGTGGGAGTGCATGTGAGCCTGGCCGGAGGAGAGTCCCCTAGCCTCTTCCAACCTTCCCACCAGGCTCTAATTTCCTTATTTATTGTATTTGCTTGTACAGCTCCATTTTGGCAAAAGTGAATTTAGATTTTCTTTCACATTCCAGTAAGTGTCTTTTTAAACTTTTTTGCAGACTTTGCATTTTGTAACCTACCCTTGAGCTACTGCATTTTGACTGAGATTTTTAAATTTTACACAGGTGATATTCTTGAATTTCATGGCCCAGAAGGAACAGGAAAAACAGAAATGCTTTATCACCTAACAGCACGATGTATACTTCCCAAATCAGAAGGTGGCCTGGAAGTAGAAGTCTTATTTATTGATACAGATTACCACTTTGATATGCTCCGGCTAGTTACAATTCTTGAGCACAGACTATCCCAAAGCTCTGAAGAAATAATCAAATACTGCCTGGGAAGATTTTTTTTGGTGTACTGCAGTAGTAGCACCCACTTACTTCTTACACTTTACTCACTAGAAAGTATGTTTTGTAGTCACCCATCTCTCTGCCTTTTGATTTTGGATAGCCTGTCAGCTTTTTACTGGATAGACCGCGTCAATGGAGGAGAAAGTGTGAACTTACAGGAGTCTACTCTGAGGAAATGTTCTCAGTGCTTAGAGAAGCTTGTAAATGACTATCGCCTGGTTCTTTTTGCAACGACACAAACTATAATGCAGAAAGCCTCGAGCTCATCAGAAGAACCTCA2499218837XRCC2c.-47-1899_459delinsAGGTTCTTCTGATGAGCTCGAGGCTTTCTGCATTATAGTTTGTGTCGTTGCAAAAAGAACCAGGCGATAGTCATTTACAAGCTTCTCTAAGCACTGAGAACATTTCCTCAGAGTAGACTCCTGTAAGTTCACACTTTCTCCTCCATTGACGCGGTCTATCCAGTAAAAAGCTGACAGGCTATCCAAAATCAAAAGGCAGAGAGATGGGTGACTACAAAACATACTTTCTAGTGAGTAAAGTGTAAGAAGTAAGTGGGTGCTACTACTGCAGTACACCAAAAAAAATCTTCCCAGGCAGTATTTGATTATTTCTTCAGAGCTTTGGGATAGTCTGTGCTCAAGAATTGTAACTAGCCGGAGCATATCAAAGTGGTAATCTGTATCAATAAATAAGACTTCTACTTCCAGGCCACCTTCTGATTTGGGAAGTATACATCGTGCTGTTAGGTGATAAAGCATTTCTGTTTTTCCTGTTCCTTCTGGGCCATGAAATTCAAGAATATCACCTGTGTAAAATTTAAAAATCTCAGTCAAAATGCAGTAGCTCAAGGGTAGGTTACAAAATGCAAAGTCTGCAAAAAAGTTTAAAAAGACACTTACTGGAATGTGAAAGAAAATCTAAATTCACTTTTGCCAAAATGGAGCTGTACAAGCAAATACAATAAATAAGGAAATTAGAGCCTGGTGGGAAGGTTGGAAGAGGCTAGGGGACTCTCCTCCGGCCAGGCTCACATGCACTCCCACTTCAATTTGTAAGATTCAAAAATAAAGAGCCACAGATCTAGGGCCTTTCCAAAATCTGATGACTACAGTACACACCCTTTCTGGTAGTTGATTACACTATATCCATTCTTCCCTTCTTCCTAAAGTATAAAACCCAATTTGATGGGGAGGGAAATGTGTCCACTTTAAAACTATTTTTCATAGTCTCCTTTGAAAAGCAAGGTTACCAGGTAACACAGCTGTCGCCAGTGAGATGCAGGCTGCTCTCTGTTGATGATTCTTTCCTATCCAGGGACCCCTTCTGCCCTGCCGCACCCTCCTGTGGGGGTGGAGCAGCCATCTGGAAGCAGTGAGGATGAAACCCACCCTTAGGATGGTGGCGTGGAAGACAGAAGGTACCCAGGACTCTGGGCACACGGAGCCCCCACCAGCCACGCACAGCCTGCCTCTGTGCCACTCAGGATGTGAGGAAAACAAGCCTCCACCTGGGCAAGCCACTAAGTTGGACTTCTATGACACGCAGGTGAAGGCACTCCCTAATTAGGTTTCTCAGTGTTATTGATGTTATGGGGGGAACAATTCTGGATTTTGTGGTTTCACACATTATTGAGGCAAGAGCCCATGGCTCTCAGACCCTAAATGCCAACAGCATCCTTCAACTGAAAACAACCTTACACGTTCCCAAACTGCCTTCAGTTATTCTTTGCTATTTGAATTATCTCTGGAAACCATGTCCAGCTGCATTAGAAATTATTTTCCTAGCATTAAAAATCAAAGTCAACTACTCTGAACGTTAAAGACTCCAACTCTCCTTCTATCTAGGCTCGAATAACTAAGGACAGCACAAGTTAAATCAAACAACACTGGGGAAGTTGCCTTGCTTCCAGAGCTTTTCAAAATGCACTCACAGTGGCATTCAACTCTTGCTTGTCATTATTAATTTACGGCTGAACTACCTGATTGGAAACACTATGTTAAAATGCCAATTATTAGCCCCAACCAAATGATGGTCTAAATACGGATTCAAGGGCTGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCAGAGGCGGGAGGATCACCTGAGGTCAGGAATTCAAGACCAGCCTGGCCAACATACTGAAACCCTACTAAAAATACAAAAAATTAGCTGGGCATGGTGGTGGGCACCTGTAATCCCAGCTACTTGAGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGACAGAGGTTGCAGTGAGCTGAGATCACGCCATTGGACTCCAGCCTGGGCGACAAGAGCGAAACTCCGTCTCAAAAAACAAAAACAAAAACACAAAAAAATGCAATTACTTTATTTCTTATTATTTAATTTTAATTTTTTTTTGAGATGGAGTCTTGTTCTGTTGCCTAGGCTGGAGTGCAGTGGTTCAATCTTGGCTTACTGCAACTTTCGCCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGTGCGCTACCGCGCCCAGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTTGCCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCTACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAACCACCGCACCTGGCCTTTCTTATTATTATCAACAAACC
c.122-1899_627delinsAGGTTCTTCTGATGAGCTCGAGGCTTTCTGCATTATAGTTTGTGTCGTTGCAAAAAGAACCAGGCGATAGTCATTTACAAGCTTCTCTAAGCACTGAGAACATTTCCTCAGAGTAGACTCCTGTAAGTTCACACTTTCTCCTCCATTGACGCGGTCTATCCAGTAAAAAGCTGACAGGCTATCCAAAATCAAAAGGCAGAGAGATGGGTGACTACAAAACATACTTTCTAGTGAGTAAAGTGTAAGAAGTAAGTGGGTGCTACTACTGCAGTACACCAAAAAAAATCTTCCCAGGCAGTATTTGATTATTTCTTCAGAGCTTTGGGATAGTCTGTGCTCAAGAATTGTAACTAGCCGGAGCATATCAAAGTGGTAATCTGTATCAATAAATAAGACTTCTACTTCCAGGCCACCTTCTGATTTGGGAAGTATACATCGTGCTGTTAGGTGATAAAGCATTTCTGTTTTTCCTGTTCCTTCTGGGCCATGAAATTCAAGAATATCACCTGTGTAAAATTTAAAAATCTCAGTCAAAATGCAGTAGCTCAAGGGTAGGTTACAAAATGCAAAGTCTGCAAAAAAGTTTAAAAAGACACTTACTGGAATGTGAAAGAAAATCTAAATTCACTTTTGCCAAAATGGAGCTGTACAAGCAAATACAATAAATAAGGAAATTAGAGCCTGGTGGGAAGGTTGGAAGAGGCTAGGGGACTCTCCTCCGGCCAGGCTCACATGCACTCCCACTTCAATTTGTAAGATTCAAAAATAAAGAGCCACAGATCTAGGGCCTTTCCAAAATCTGATGACTACAGTACACACCCTTTCTGGTAGTTGATTACACTATATCCATTCTTCCCTTCTTCCTAAAGTATAAAACCCAATTTGATGGGGAGGGAAATGTGTCCACTTTAAAACTATTTTTCATAGTCTCCTTTGAAAAGCAAGGTTACCAGGTAACACAGCTGTCGCCAGTGAGATGCAGGCTGCTCTCTGTTGATGATTCTTTCCTATCCAGGGACCCCTTCTGCCCTGCCGCACCCTCCTGTGGGGGTGGAGCAGCCATCTGGAAGCAGTGAGGATGAAACCCACCCTTAGGATGGTGGCGTGGAAGACAGAAGGTACCCAGGACTCTGGGCACACGGAGCCCCCACCAGCCACGCACAGCCTGCCTCTGTGCCACTCAGGATGTGAGGAAAACAAGCCTCCACCTGGGCAAGCCACTAAGTTGGACTTCTATGACACGCAGGTGAAGGCACTCCCTAATTAGGTTTCTCAGTGTTATTGATGTTATGGGGGGAACAATTCTGGATTTTGTGGTTTCACACATTATTGAGGCAAGAGCCCATGGCTCTCAGACCCTAAATGCCAACAGCATCCTTCAACTGAAAACAACCTTACACGTTCCCAAACTGCCTTCAGTTATTCTTTGCTATTTGAATTATCTCTGGAAACCATGTCCAGCTGCATTAGAAATTATTTTCCTAGCATTAAAAATCAAAGTCAACTACTCTGAACGTTAAAGACTCCAACTCTCCTTCTATCTAGGCTCGAATAACTAAGGACAGCACAAGTTAAATCAAACAACACTGGGGAAGTTGCCTTGCTTCCAGAGCTTTTCAAAATGCACTCACAGTGGCATTCAACTCTTGCTTGTCATTATTAATTTACGGCTGAACTACCTGATTGGAAACACTATGTTAAAATGCCAATTATTAGCCCCAACCAAATGATGGTCTAAATACGGATTCAAGGGCTGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCAGAGGCGGGAGGATCACCTGAGGTCAGGAATTCAAGACCAGCCTGGCCAACATACTGAAACCCTACTAAAAATACAAAAAATTAGCTGGGCATGGTGGTGGGCACCTGTAATCCCAGCTACTTGAGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGACAGAGGTTGCAGTGAGCTGAGATCACGCCATTGGACTCCAGCCTGGGCGACAAGAGCGAAACTCCGTCTCAAAAAACAAAAACAAAAACACAAAAAAATGCAATTACTTTATTTCTTATTATTTAATTTTAATTTTTTTTTGAGATGGAGTCTTGTTCTGTTGCCTAGGCTGGAGTGCAGTGGTTCAATCTTGGCTTACTGCAACTTTCGCCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGTGCGCTACCGCGCCCAGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTTGCCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCTACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAACCACCGCACCTGGCCTTTCTTATTATTATCAACAAACC
n.144-1899_649delinsAGGTTCTTCTGATGAGCTCGAGGCTTTCTGCATTATAGTTTGTGTCGTTGCAAAAAGAACCAGGCGATAGTCATTTACAAGCTTCTCTAAGCACTGAGAACATTTCCTCAGAGTAGACTCCTGTAAGTTCACACTTTCTCCTCCATTGACGCGGTCTATCCAGTAAAAAGCTGACAGGCTATCCAAAATCAAAAGGCAGAGAGATGGGTGACTACAAAACATACTTTCTAGTGAGTAAAGTGTAAGAAGTAAGTGGGTGCTACTACTGCAGTACACCAAAAAAAATCTTCCCAGGCAGTATTTGATTATTTCTTCAGAGCTTTGGGATAGTCTGTGCTCAAGAATTGTAACTAGCCGGAGCATATCAAAGTGGTAATCTGTATCAATAAATAAGACTTCTACTTCCAGGCCACCTTCTGATTTGGGAAGTATACATCGTGCTGTTAGGTGATAAAGCATTTCTGTTTTTCCTGTTCCTTCTGGGCCATGAAATTCAAGAATATCACCTGTGTAAAATTTAAAAATCTCAGTCAAAATGCAGTAGCTCAAGGGTAGGTTACAAAATGCAAAGTCTGCAAAAAAGTTTAAAAAGACACTTACTGGAATGTGAAAGAAAATCTAAATTCACTTTTGCCAAAATGGAGCTGTACAAGCAAATACAATAAATAAGGAAATTAGAGCCTGGTGGGAAGGTTGGAAGAGGCTAGGGGACTCTCCTCCGGCCAGGCTCACATGCACTCCCACTTCAATTTGTAAGATTCAAAAATAAAGAGCCACAGATCTAGGGCCTTTCCAAAATCTGATGACTACAGTACACACCCTTTCTGGTAGTTGATTACACTATATCCATTCTTCCCTTCTTCCTAAAGTATAAAACCCAATTTGATGGGGAGGGAAATGTGTCCACTTTAAAACTATTTTTCATAGTCTCCTTTGAAAAGCAAGGTTACCAGGTAACACAGCTGTCGCCAGTGAGATGCAGGCTGCTCTCTGTTGATGATTCTTTCCTATCCAGGGACCCCTTCTGCCCTGCCGCACCCTCCTGTGGGGGTGGAGCAGCCATCTGGAAGCAGTGAGGATGAAACCCACCCTTAGGATGGTGGCGTGGAAGACAGAAGGTACCCAGGACTCTGGGCACACGGAGCCCCCACCAGCCACGCACAGCCTGCCTCTGTGCCACTCAGGATGTGAGGAAAACAAGCCTCCACCTGGGCAAGCCACTAAGTTGGACTTCTATGACACGCAGGTGAAGGCACTCCCTAATTAGGTTTCTCAGTGTTATTGATGTTATGGGGGGAACAATTCTGGATTTTGTGGTTTCACACATTATTGAGGCAAGAGCCCATGGCTCTCAGACCCTAAATGCCAACAGCATCCTTCAACTGAAAACAACCTTACACGTTCCCAAACTGCCTTCAGTTATTCTTTGCTATTTGAATTATCTCTGGAAACCATGTCCAGCTGCATTAGAAATTATTTTCCTAGCATTAAAAATCAAAGTCAACTACTCTGAACGTTAAAGACTCCAACTCTCCTTCTATCTAGGCTCGAATAACTAAGGACAGCACAAGTTAAATCAAACAACACTGGGGAAGTTGCCTTGCTTCCAGAGCTTTTCAAAATGCACTCACAGTGGCATTCAACTCTTGCTTGTCATTATTAATTTACGGCTGAACTACCTGATTGGAAACACTATGTTAAAATGCCAATTATTAGCCCCAACCAAATGATGGTCTAAATACGGATTCAAGGGCTGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCAGAGGCGGGAGGATCACCTGAGGTCAGGAATTCAAGACCAGCCTGGCCAACATACTGAAACCCTACTAAAAATACAAAAAATTAGCTGGGCATGGTGGTGGGCACCTGTAATCCCAGCTACTTGAGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGACAGAGGTTGCAGTGAGCTGAGATCACGCCATTGGACTCCAGCCTGGGCGACAAGAGCGAAACTCCGTCTCAAAAAACAAAAACAAAAACACAAAAAAATGCAATTACTTTATTTCTTATTATTTAATTTTAATTTTTTTTTGAGATGGAGTCTTGTTCTGTTGCCTAGGCTGGAGTGCAGTGGTTCAATCTTGGCTTACTGCAACTTTCGCCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGTGCGCTACCGCGCCCAGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTTGCCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCTACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAACCACCGCACCTGGCCTTTCTTATTATTATCAACAAACC
 ClinVar
7g.152648859G>ACA370198291XRCC2c.458C>T (p.Pro153Leu)
c.626C>T (p.Pro209Leu)
n.648C>T
7g.152648859G>CCA370198292XRCC2c.458C>G (p.Pro153Arg)
c.626C>G (p.Pro209Arg)
n.648C>G
7g.152648859G=CA1753246932XRCC2c.458C= (p.Pro153=)
c.626C= (p.Pro209=)
n.648C=
7g.152648859G>TCA370198293XRCC2c.458C>A (p.Pro153His)
c.626C>A (p.Pro209His)
n.648C>A
 dbSNP COSMIC
7g.152648860G>ACA4582318XRCC2c.457C>T (p.Pro153Ser)
c.625C>T (p.Pro209Ser)
n.647C>T
 dbSNP ExAC gnomAD v2
7g.152648860G>CCA370198294XRCC2c.457C>G (p.Pro153Ala)
c.625C>G (p.Pro209Ala)
n.647C>G
7g.152648860G=CA1753246937XRCC2c.457C= (p.Pro153=)
c.625C= (p.Pro209=)
n.647C=
7g.152648860G>TCA4582319XRCC2c.457C>A (p.Pro153Thr)
c.625C>A (p.Pro209Thr)
n.647C>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.152648860_152648863delinsGTTCCA1753246940XRCC2c.454_457delinsGAAC (p.Glu152=)
c.622_625delinsGAAC (p.Glu208=)
n.644_647delinsGAAC
7g.152648861T>ACA370198296XRCC2c.456A>T (p.Glu152Asp)
c.624A>T (p.Glu208Asp)
n.646A>T
 ClinVar
7g.152648861T>CCA458895369XRCC2c.456A>G (p.Glu152=)
c.624A>G (p.Glu208=)
n.646A>G
 COSMIC
7g.152648861T>GCA370198295XRCC2c.456A>C (p.Glu152Asp)
c.624A>C (p.Glu208Asp)
n.646A>C
7g.152648861_152648862insGGTTCA2685735794XRCC2c.456_457insACCA (p.Pro153ThrfsTer11)
c.624_625insACCA (p.Pro209ThrfsTer11)
n.646_647insACCA
 gnomAD v4
7g.152648865_152648867delCA1753246944XRCC2c.454_456del (p.Glu152del)
c.622_624del (p.Glu208del)
n.644_646del
 ClinVar dbSNP
7g.152648862_152648884delCA2685735797XRCC2c.434_456del (p.Lys145ThrfsTer10)
c.602_624del (p.Lys201ThrfsTer10)
n.624_646del
 gnomAD v4
7g.152648861_152648862insGGCA2685735802XRCC2c.455_456insCC (p.Glu152AspfsTer15)
c.623_624insCC (p.Glu208AspfsTer15)
n.645_646insCC
 gnomAD v4
7g.152648862T>ACA370198297XRCC2c.455A>T (p.Glu152Val)
c.623A>T (p.Glu208Val)
n.645A>T
7g.152648862T>CCA370198299XRCC2c.455A>G (p.Glu152Gly)
c.623A>G (p.Glu208Gly)
n.645A>G
 ClinVar
7g.152648862T>GCA370198298XRCC2c.455A>C (p.Glu152Ala)
c.623A>C (p.Glu208Ala)
n.645A>C
7g.152648862_152648863insTTGTTGATAATAATAAGAAAGGCCAGGTGCGGTGGTTCACACCTGTAATCCCAGCACA2685735805XRCC2c.454_455insTGCTGGGATTACAGGTGTGAACCACCGCACCTGGCCTTTCTTATTATTATCAACAA (p.Glu152ValfsTer7)
c.622_623insTGCTGGGATTACAGGTGTGAACCACCGCACCTGGCCTTTCTTATTATTATCAACAA (p.Glu208ValfsTer7)
n.644_645insTGCTGGGATTACAGGTGTGAACCACCGCACCTGGCCTTTCTTATTATTATCAACAA
 gnomAD v4
7g.152648863C>ACA370198300XRCC2c.454G>T (p.Glu152Ter)
c.622G>T (p.Glu208Ter)
n.644G>T
 gnomAD v4
7g.152648863C>GCA370198301XRCC2c.454G>C (p.Glu152Gln)
c.622G>C (p.Glu208Gln)
n.644G>C
 gnomAD v4
7g.152648863C>TCA370198302XRCC2c.454G>A (p.Glu152Lys)
c.622G>A (p.Glu208Lys)
n.644G>A
7g.152648864T>ACA370198303XRCC2c.453A>T (p.Glu151Asp)
c.621A>T (p.Glu207Asp)
n.643A>T
 ClinVar
7g.152648864T>CCA458895372XRCC2c.453A>G (p.Glu151=)
c.621A>G (p.Glu207=)
n.643A>G
7g.152648864T>GCA370198304XRCC2c.453A>C (p.Glu151Asp)
c.621A>C (p.Glu207Asp)
n.643A>C
7g.152648865T>ACA370198305XRCC2c.452A>T (p.Glu151Val)
c.620A>T (p.Glu207Val)
n.642A>T
7g.152648865T>CCA288141XRCC2c.452A>G (p.Glu151Gly)
c.620A>G (p.Glu207Gly)
n.642A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648865T>GCA370198306XRCC2c.452A>C (p.Glu151Ala)
c.620A>C (p.Glu207Ala)
n.642A>C
7g.152648865T=CA1753246948XRCC2c.452A= (p.Glu151=)
c.620A= (p.Glu207=)
n.642A=
7g.152648865_152648866insGATAATAATAAGAAAGGCCA2685735817XRCC2c.451_452insGCCTTTCTTATTATTATC (p.Glu151delinsGlyLeuSerTyrTyrTyrGln)
c.619_620insGCCTTTCTTATTATTATC (p.Glu207delinsGlyLeuSerTyrTyrTyrGln)
n.641_642insGCCTTTCTTATTATTATC
 gnomAD v4
7g.152648865_152648866insGATAATAATAAGAAAGGCCAGGTGCGGTGGTTCACA2685735818XRCC2c.451_452insTGAACCACCGCACCTGGCCTTTCTTATTATTATC (p.Glu151ValfsTer23)
c.619_620insTGAACCACCGCACCTGGCCTTTCTTATTATTATC (p.Glu207ValfsTer23)
n.641_642insTGAACCACCGCACCTGGCCTTTCTTATTATTATC
 gnomAD v4
7g.152648866C>ACA370198307XRCC2c.451G>T (p.Glu151Ter)
c.619G>T (p.Glu207Ter)
n.641G>T
7g.152648866C=CA1753246957XRCC2c.451G= (p.Glu151=)
c.619G= (p.Glu207=)
n.641G=
7g.152648866C>GCA4582320XRCC2c.451G>C (p.Glu151Gln)
c.619G>C (p.Glu207Gln)
n.641G>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.152648866C>TCA370198308XRCC2c.451G>A (p.Glu151Lys)
c.619G>A (p.Glu207Lys)
n.641G>A
 ClinVar dbSNP gnomAD v4
7g.152648867T>ACA458895373XRCC2c.450A>T (p.Ser150=)
c.618A>T (p.Ser206=)
n.640A>T
7g.152648867T>CCA458895374XRCC2c.450A>G (p.Ser150=)
c.618A>G (p.Ser206=)
n.640A>G
 dbSNP gnomAD v4
7g.152648867T>GCA458895375XRCC2c.450A>C (p.Ser150=)
c.618A>C (p.Ser206=)
n.640A>C
7g.152648867T=CA1753246960XRCC2c.450A= (p.Ser150=)
c.618A= (p.Ser206=)
n.640A=
7g.152648868G>ACA370198311XRCC2c.449C>T (p.Ser150Leu)
c.617C>T (p.Ser206Leu)
n.639C>T
 ClinVar dbSNP
7g.152648868G>CCA370198309XRCC2c.449C>G (p.Ser150Ter)
c.617C>G (p.Ser206Ter)
n.639C>G
7g.152648868G=CA1753246964XRCC2c.449C= (p.Ser150=)
c.617C= (p.Ser206=)
n.639C=
7g.152648868G>TCA370198310XRCC2c.449C>A (p.Ser150Ter)
c.617C>A (p.Ser206Ter)
n.639C>A
7g.152648869A>CCA370198312XRCC2c.448T>G (p.Ser150Ala)
c.616T>G (p.Ser206Ala)
n.638T>G
 ClinVar gnomAD v4
7g.152648869A>GCA370198313XRCC2c.448T>C (p.Ser150Pro)
c.616T>C (p.Ser206Pro)
n.638T>C
 gnomAD v4
7g.152648869A>TCA370198314XRCC2c.448T>A (p.Ser150Thr)
c.616T>A (p.Ser206Thr)
n.638T>A
7g.152648870T>ACA458895377XRCC2c.447A>T (p.Ser149=)
c.615A>T (p.Ser205=)
n.637A>T
7g.152648870T>CCA458895378XRCC2c.447A>G (p.Ser149=)
c.615A>G (p.Ser205=)
n.637A>G
7g.152648870T>GCA458895379XRCC2c.447A>C (p.Ser149=)
c.615A>C (p.Ser205=)
n.637A>C
7g.152648871G>ACA370198315XRCC2c.446C>T (p.Ser149Leu)
c.614C>T (p.Ser205Leu)
n.636C>T
 ClinVar dbSNP
7g.152648871G>CCA370198316XRCC2c.446C>G (p.Ser149Ter)
c.614C>G (p.Ser205Ter)
n.636C>G
7g.152648871G>TCA370198317XRCC2c.446C>A (p.Ser149Ter)
c.614C>A (p.Ser205Ter)
n.636C>A
7g.152648872A=CA1753246967XRCC2c.445T= (p.Ser149=)
c.613T= (p.Ser205=)
n.635T=
7g.152648872A>CCA300477XRCC2c.445T>G (p.Ser149Ala)
c.613T>G (p.Ser205Ala)
n.635T>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648872A>GCA370198318XRCC2c.445T>C (p.Ser149Pro)
c.613T>C (p.Ser205Pro)
n.635T>C
7g.152648872A>TCA370198319XRCC2c.445T>A (p.Ser149Thr)
c.613T>A (p.Ser205Thr)
n.635T>A
7g.152648873G>ACA458895380XRCC2c.444C>T (p.Ser148=)
c.612C>T (p.Ser204=)
n.634C>T
 ClinVar
7g.152648873G>CCA4582321XRCC2c.444C>G (p.Ser148Arg)
c.612C>G (p.Ser204Arg)
n.634C>G
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.152648873G=CA1753246971XRCC2c.444C= (p.Ser148=)
c.612C= (p.Ser204=)
n.634C=
7g.152648873G>TCA370198320XRCC2c.444C>A (p.Ser148Arg)
c.612C>A (p.Ser204Arg)
n.634C>A
7g.152648874C>ACA370198321XRCC2c.443G>T (p.Ser148Ile)
c.611G>T (p.Ser204Ile)
n.633G>T
7g.152648874C=CA1753246974XRCC2c.443G= (p.Ser148=)
c.611G= (p.Ser204=)
n.633G=
7g.152648874C>GCA370198322XRCC2c.443G>C (p.Ser148Thr)
c.611G>C (p.Ser204Thr)
n.633G>C
 ClinVar dbSNP gnomAD v2
7g.152648874C>TCA4582322XRCC2c.443G>A (p.Ser148Asn)
c.611G>A (p.Ser204Asn)
n.633G>A
 ClinVar dbSNP ExAC gnomAD v2
7g.152648875T>ACA370198323XRCC2c.442A>T (p.Ser148Cys)
c.610A>T (p.Ser204Cys)
n.632A>T
 dbSNP
7g.152648875T>CCA370198324XRCC2c.442A>G (p.Ser148Gly)
c.610A>G (p.Ser204Gly)
n.632A>G
 dbSNP
7g.152648875T>GCA370198325XRCC2c.442A>C (p.Ser148Arg)
c.610A>C (p.Ser204Arg)
n.632A>C
7g.152648876delCA2580077740XRCC2c.441del (p.Ser148AlafsTer18)
c.609del (p.Ser204AlafsTer18)
n.631del
 ClinVar
7g.152648876C>ACA458895384XRCC2c.441G>T (p.Ser147=)
c.609G>T (p.Ser203=)
n.631G>T
7g.152648876C=CA1753246978XRCC2c.441G= (p.Ser147=)
c.609G= (p.Ser203=)
n.631G=
7g.152648876C>GCA4582323XRCC2c.441G>C (p.Ser147=)
c.609G>C (p.Ser203=)
n.631G>C
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648876C>TCA458895385XRCC2c.441G>A (p.Ser147=)
c.609G>A (p.Ser203=)
n.631G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
7g.152648877G>ACA10582474XRCC2c.440C>T (p.Ser147Leu)
c.608C>T (p.Ser203Leu)
n.630C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.152648877G>CCA370198326XRCC2c.440C>G (p.Ser147Trp)
c.608C>G (p.Ser203Trp)
n.630C>G
 gnomAD v4
7g.152648877G=CA1753246984XRCC2c.440C= (p.Ser147=)
c.608C= (p.Ser203=)
n.630C=
7g.152648877G>TCA370198327XRCC2c.440C>A (p.Ser147Ter)
c.608C>A (p.Ser203Ter)
n.630C>A
7g.152648878A=CA1753246988XRCC2c.439T= (p.Ser147=)
c.607T= (p.Ser203=)
n.629T=
7g.152648878A>CCA370198328XRCC2c.439T>G (p.Ser147Ala)
c.607T>G (p.Ser203Ala)
n.629T>G
 ClinVar dbSNP
7g.152648878A>GCA370198329XRCC2c.439T>C (p.Ser147Pro)
c.607T>C (p.Ser203Pro)
n.629T>C
 gnomAD v4
7g.152648878A>TCA370198330XRCC2c.439T>A (p.Ser147Thr)
c.607T>A (p.Ser203Thr)
n.629T>A
7g.152648879G>ACA458895388XRCC2c.438C>T (p.Ala146=)
c.606C>T (p.Ala202=)
n.628C>T
7g.152648879G>CCA458895389XRCC2c.438C>G (p.Ala146=)
c.606C>G (p.Ala202=)
n.628C>G
7g.152648879G>TCA458895390XRCC2c.438C>A (p.Ala146=)
c.606C>A (p.Ala202=)
n.628C>A
7g.152648880G>ACA370198331XRCC2c.437C>T (p.Ala146Val)
c.605C>T (p.Ala202Val)
n.627C>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.152648880G>CCA370198332XRCC2c.437C>G (p.Ala146Gly)
c.605C>G (p.Ala202Gly)
n.627C>G
7g.152648880G=CA1753246991XRCC2c.437C= (p.Ala146=)
c.605C= (p.Ala202=)
n.627C=
7g.152648880G>TCA370198333XRCC2c.437C>A (p.Ala146Asp)
c.605C>A (p.Ala202Asp)
n.627C>A
 dbSNP gnomAD v4
7g.152648881C>ACA370198336XRCC2c.436G>T (p.Ala146Ser)
c.604G>T (p.Ala202Ser)
n.626G>T
 dbSNP
7g.152648881C>GCA370198335XRCC2c.436G>C (p.Ala146Pro)
c.604G>C (p.Ala202Pro)
n.626G>C
7g.152648881C>TCA370198334XRCC2c.436G>A (p.Ala146Thr)
c.604G>A (p.Ala202Thr)
n.626G>A
7g.152648882T>ACA370198337XRCC2c.435A>T (p.Lys145Asn)
c.603A>T (p.Lys201Asn)
n.625A>T
7g.152648882T>CCA458895393XRCC2c.435A>G (p.Lys145=)
c.603A>G (p.Lys201=)
n.625A>G
7g.152648882T>GCA370198338XRCC2c.435A>C (p.Lys145Asn)
c.603A>C (p.Lys201Asn)
n.625A>C
 gnomAD v4
7g.152648884delCA2573141904XRCC2c.435del (p.Ala146ProfsTer20)
c.603del (p.Ala202ProfsTer20)
n.625del
 ClinVar dbSNP
7g.152648883T>ACA370198339XRCC2c.434A>T (p.Lys145Ile)
c.602A>T (p.Lys201Ile)
n.624A>T
7g.152648883T>CCA370198340XRCC2c.434A>G (p.Lys145Arg)
c.602A>G (p.Lys201Arg)
n.624A>G
7g.152648883T>GCA370198341XRCC2c.434A>C (p.Lys145Thr)
c.602A>C (p.Lys201Thr)
n.624A>C
7g.152648884T>ACA370198342XRCC2c.433A>T (p.Lys145Ter)
c.601A>T (p.Lys201Ter)
n.623A>T
7g.152648884T>CCA370198343XRCC2c.433A>G (p.Lys145Glu)
c.601A>G (p.Lys201Glu)
n.623A>G
7g.152648884T>GCA370198344XRCC2c.433A>C (p.Lys145Gln)
c.601A>C (p.Lys201Gln)
n.623A>C
7g.152648885C>ACA370198345XRCC2c.432G>T (p.Gln144His)
c.600G>T (p.Gln200His)
n.622G>T
7g.152648885C>GCA370198346XRCC2c.432G>C (p.Gln144His)
c.600G>C (p.Gln200His)
n.622G>C
7g.152648885C>TCA458895396XRCC2c.432G>A (p.Gln144=)
c.600G>A (p.Gln200=)
n.622G>A
 dbSNP
7g.152648886T>ACA370198347XRCC2c.431A>T (p.Gln144Leu)
c.599A>T (p.Gln200Leu)
n.621A>T
7g.152648886T>CCA370198348XRCC2c.431A>G (p.Gln144Arg)
c.599A>G (p.Gln200Arg)
n.621A>G
7g.152648886T>GCA4582324XRCC2c.431A>C (p.Gln144Pro)
c.599A>C (p.Gln200Pro)
n.621A>C
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.152648886T=CA1753246994XRCC2c.431A= (p.Gln144=)
c.599A= (p.Gln200=)
n.621A=
7g.152648887G>ACA370198351XRCC2c.430C>T (p.Gln144Ter)
c.598C>T (p.Gln200Ter)
n.620C>T
 ClinVar dbSNP gnomAD v4
7g.152648887G>CCA370198350XRCC2c.430C>G (p.Gln144Glu)
c.598C>G (p.Gln200Glu)
n.620C>G
7g.152648887G=CA1753246995XRCC2c.430C= (p.Gln144=)
c.598C= (p.Gln200=)
n.620C=
7g.152648887G>TCA370198349XRCC2c.430C>A (p.Gln144Lys)
c.598C>A (p.Gln200Lys)
n.620C>A
7g.152648888C>ACA370198352XRCC2c.429G>T (p.Met143Ile)
c.597G>T (p.Met199Ile)
n.619G>T
 gnomAD v4
7g.152648888C>GCA370198354XRCC2c.429G>C (p.Met143Ile)
c.597G>C (p.Met199Ile)
n.619G>C
7g.152648888C>TCA370198353XRCC2c.429G>A (p.Met143Ile)
c.597G>A (p.Met199Ile)
n.619G>A
 dbSNP
7g.152648889A=CA1753247004XRCC2c.428T= (p.Met143=)
c.596T= (p.Met199=)
n.618T=
7g.152648889A>CCA370198355XRCC2c.428T>G (p.Met143Arg)
c.596T>G (p.Met199Arg)
n.618T>G
 dbSNP gnomAD v4
7g.152648889A>GCA300475XRCC2c.428T>C (p.Met143Thr)
c.596T>C (p.Met199Thr)
n.618T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648889A>TCA10584277XRCC2c.428T>A (p.Met143Lys)
c.596T>A (p.Met199Lys)
n.618T>A
 ClinVar dbSNP gnomAD v4
7g.152648890T>ACA370198356XRCC2c.427A>T (p.Met143Leu)
c.595A>T (p.Met199Leu)
n.617A>T
7g.152648890T>CCA370198357XRCC2c.427A>G (p.Met143Val)
c.595A>G (p.Met199Val)
n.617A>G
7g.152648890T>GCA370198358XRCC2c.427A>C (p.Met143Leu)
c.595A>C (p.Met199Leu)
n.617A>C
 ClinVar dbSNP
7g.152648890T=CA1753247013XRCC2c.427A= (p.Met143=)
c.595A= (p.Met199=)
n.617A=
7g.152648891T>ACA458895398XRCC2c.426A>T (p.Ile142=)
c.594A>T (p.Ile198=)
n.616A>T
7g.152648891T>CCA370198359XRCC2c.426A>G (p.Ile142Met)
c.594A>G (p.Ile198Met)
n.616A>G
7g.152648891T>GCA458895400XRCC2c.426A>C (p.Ile142=)
c.594A>C (p.Ile198=)
n.616A>C
7g.152648892A>CCA370198360XRCC2c.425T>G (p.Ile142Arg)
c.593T>G (p.Ile198Arg)
n.615T>G
7g.152648892A>GCA370198361XRCC2c.425T>C (p.Ile142Thr)
c.593T>C (p.Ile198Thr)
n.615T>C
7g.152648892A>TCA370198362XRCC2c.425T>A (p.Ile142Lys)
c.593T>A (p.Ile198Lys)
n.615T>A
7g.152648893T>ACA370198363XRCC2c.424A>T (p.Ile142Leu)
c.592A>T (p.Ile198Leu)
n.614A>T
7g.152648893T>CCA169486945XRCC2c.424A>G (p.Ile142Val)
c.592A>G (p.Ile198Val)
n.614A>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.152648893T>GCA370198364XRCC2c.424A>C (p.Ile142Leu)
c.592A>C (p.Ile198Leu)
n.614A>C
7g.152648893T=CA1753247020XRCC2c.424A= (p.Ile142=)
c.592A= (p.Ile198=)
n.614A=
7g.152648894A=CA1753247028XRCC2c.423T= (p.Thr141=)
c.591T= (p.Thr197=)
n.613T=
7g.152648894A>CCA458895403XRCC2c.423T>G (p.Thr141=)
c.591T>G (p.Thr197=)
n.613T>G
7g.152648894A>GCA458895404XRCC2c.423T>C (p.Thr141=)
c.591T>C (p.Thr197=)
n.613T>C
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.152648894A>TCA458895405XRCC2c.423T>A (p.Thr141=)
c.591T>A (p.Thr197=)
n.613T>A
7g.152648895G>ACA370198367XRCC2c.422C>T (p.Thr141Ile)
c.590C>T (p.Thr197Ile)
n.612C>T
7g.152648895G>CCA370198366XRCC2c.422C>G (p.Thr141Ser)
c.590C>G (p.Thr197Ser)
n.612C>G
 dbSNP gnomAD v4
7g.152648895G=CA1753247031XRCC2c.422C= (p.Thr141=)
c.590C= (p.Thr197=)
n.612C=
7g.152648895G>TCA370198365XRCC2c.422C>A (p.Thr141Asn)
c.590C>A (p.Thr197Asn)
n.612C>A
7g.152648896T>ACA370198368XRCC2c.421A>T (p.Thr141Ser)
c.589A>T (p.Thr197Ser)
n.611A>T
7g.152648896T>CCA370198369XRCC2c.421A>G (p.Thr141Ala)
c.589A>G (p.Thr197Ala)
n.611A>G
 COSMIC
7g.152648896T>GCA370198370XRCC2c.421A>C (p.Thr141Pro)
c.589A>C (p.Thr197Pro)
n.611A>C
7g.152648897T>ACA370198371XRCC2c.420A>T (p.Gln140His)
c.588A>T (p.Gln196His)
n.610A>T
7g.152648897T>CCA458895407XRCC2c.420A>G (p.Gln140=)
c.588A>G (p.Gln196=)
n.610A>G
 ClinVar dbSNP
7g.152648897T>GCA370198372XRCC2c.420A>C (p.Gln140His)
c.588A>C (p.Gln196His)
n.610A>C
7g.152648897T=CA1753247036XRCC2c.420A= (p.Gln140=)
c.588A= (p.Gln196=)
n.610A=
7g.152648898T>ACA370198373XRCC2c.419A>T (p.Gln140Leu)
c.587A>T (p.Gln196Leu)
n.609A>T
7g.152648898T>CCA370198374XRCC2c.419A>G (p.Gln140Arg)
c.587A>G (p.Gln196Arg)
n.609A>G
7g.152648898T>GCA4582325XRCC2c.419A>C (p.Gln140Pro)
c.587A>C (p.Gln196Pro)
n.609A>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.152648898T=CA1753247038XRCC2c.419A= (p.Gln140=)
c.587A= (p.Gln196=)
n.609A=
7g.152648899G>ACA370198375XRCC2c.418C>T (p.Gln140Ter)
c.586C>T (p.Gln196Ter)
n.608C>T
7g.152648899G>CCA370198376XRCC2c.418C>G (p.Gln140Glu)
c.586C>G (p.Gln196Glu)
n.608C>G
7g.152648899G=CA1753247043XRCC2c.418C= (p.Gln140=)
c.586C= (p.Gln196=)
n.608C=
7g.152648899G>TCA370198377XRCC2c.418C>A (p.Gln140Lys)
c.586C>A (p.Gln196Lys)
n.608C>A
 ClinVar dbSNP
7g.152648900T>ACA458895409XRCC2c.417A>T (p.Thr139=)
c.585A>T (p.Thr195=)
n.607A>T
 ClinVar
7g.152648900T>CCA458895411XRCC2c.417A>G (p.Thr139=)
c.585A>G (p.Thr195=)
n.607A>G
7g.152648900T>GCA458895413XRCC2c.417A>C (p.Thr139=)
c.585A>C (p.Thr195=)
n.607A>C
7g.152648901G>ACA370198379XRCC2c.416C>T (p.Thr139Ile)
c.584C>T (p.Thr195Ile)
n.606C>T
 dbSNP
7g.152648901G>CCA370198380XRCC2c.416C>G (p.Thr139Arg)
c.584C>G (p.Thr195Arg)
n.606C>G
7g.152648901G>TCA370198378XRCC2c.416C>A (p.Thr139Lys)
c.584C>A (p.Thr195Lys)
n.606C>A
7g.152648902T>ACA370198381XRCC2c.415A>T (p.Thr139Ser)
c.583A>T (p.Thr195Ser)
n.605A>T
7g.152648902T>CCA370198382XRCC2c.415A>G (p.Thr139Ala)
c.583A>G (p.Thr195Ala)
n.605A>G
7g.152648902T>GCA370198383XRCC2c.415A>C (p.Thr139Pro)
c.583A>C (p.Thr195Pro)
n.605A>C
7g.152648903C>ACA458895415XRCC2c.414G>T (p.Thr138=)
c.582G>T (p.Thr194=)
n.604G>T
 ClinVar dbSNP
7g.152648903C=CA1753247051XRCC2c.414G= (p.Thr138=)
c.582G= (p.Thr194=)
n.604G=
7g.152648903C>GCA458895416XRCC2c.414G>C (p.Thr138=)
c.582G>C (p.Thr194=)
n.604G>C
 dbSNP
7g.152648903C>TCA4582326XRCC2c.414G>A (p.Thr138=)
c.582G>A (p.Thr194=)
n.604G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648904G>ACA4582327XRCC2c.413C>T (p.Thr138Met)
c.581C>T (p.Thr194Met)
n.603C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
7g.152648904G>CCA370198384XRCC2c.413C>G (p.Thr138Arg)
c.581C>G (p.Thr194Arg)
n.603C>G
7g.152648904G=CA1753247061XRCC2c.413C= (p.Thr138=)
c.581C= (p.Thr194=)
n.603C=
7g.152648904G>TCA370198385XRCC2c.413C>A (p.Thr138Lys)
c.581C>A (p.Thr194Lys)
n.603C>A
7g.152648905T>ACA370198386XRCC2c.412A>T (p.Thr138Ser)
c.580A>T (p.Thr194Ser)
n.602A>T
7g.152648905T>CCA288139XRCC2c.412A>G (p.Thr138Ala)
c.580A>G (p.Thr194Ala)
n.602A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648905T>GCA370198387XRCC2c.412A>C (p.Thr138Pro)
c.580A>C (p.Thr194Pro)
n.602A>C
7g.152648905T=CA1753247063XRCC2c.412A= (p.Thr138=)
c.580A= (p.Thr194=)
n.602A=
7g.152648906T>ACA458895418XRCC2c.411A>T (p.Ala137=)
c.579A>T (p.Ala193=)
n.601A>T
7g.152648906T>CCA458895419XRCC2c.411A>G (p.Ala137=)
c.579A>G (p.Ala193=)
n.601A>G
7g.152648906T>GCA458895420XRCC2c.411A>C (p.Ala137=)
c.579A>C (p.Ala193=)
n.601A>C
7g.152648907G>ACA370198388XRCC2c.410C>T (p.Ala137Val)
c.578C>T (p.Ala193Val)
n.600C>T
 ClinVar dbSNP gnomAD v4
7g.152648907G>CCA370198389XRCC2c.410C>G (p.Ala137Gly)
c.578C>G (p.Ala193Gly)
n.600C>G
7g.152648907G>TCA370198390XRCC2c.410C>A (p.Ala137Glu)
c.578C>A (p.Ala193Glu)
n.600C>A
7g.152648909_152648922delCA2685735866XRCC2c.397_410del (p.Leu133AsnfsTer25)
c.565_578del (p.Leu189AsnfsTer25)
n.587_600del
 gnomAD v4
7g.152648908C>ACA370198393XRCC2c.409G>T (p.Ala137Ser)
c.577G>T (p.Ala193Ser)
n.599G>T
7g.152648908C=CA1753247067XRCC2c.409G= (p.Ala137=)
c.577G= (p.Ala193=)
n.599G=
7g.152648908C>GCA370198392XRCC2c.409G>C (p.Ala137Pro)
c.577G>C (p.Ala193Pro)
n.599G>C
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.152648908C>TCA370198391XRCC2c.409G>A (p.Ala137Thr)
c.577G>A (p.Ala193Thr)
n.599G>A
 dbSNP
7g.152648909A=CA1753247071XRCC2c.408T= (p.Phe136=)
c.576T= (p.Phe192=)
n.598T=
7g.152648909A>CCA370198394XRCC2c.408T>G (p.Phe136Leu)
c.576T>G (p.Phe192Leu)
n.598T>G
7g.152648909A>GCA4582328XRCC2c.408T>C (p.Phe136=)
c.576T>C (p.Phe192=)
n.598T>C
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.152648909A>TCA370198395XRCC2c.408T>A (p.Phe136Leu)
c.576T>A (p.Phe192Leu)
n.598T>A
7g.152648913_152648914insAAAAAAAAACA2778474393XRCC2c.408_409insTTTTTTTTT (p.Phe136_Ala137insPhePhePhe)
c.576_577insTTTTTTTTT (p.Phe192_Ala193insPhePhePhe)
n.598_599insTTTTTTTTT
7g.152648913delCA2778474395XRCC2c.408del (p.Phe136LeufsTer7)
c.576del (p.Phe192LeufsTer7)
n.598del
7g.152648910A>CCA370198396XRCC2c.407T>G (p.Phe136Cys)
c.575T>G (p.Phe192Cys)
n.597T>G
7g.152648910A>GCA370198397XRCC2c.407T>C (p.Phe136Ser)
c.575T>C (p.Phe192Ser)
n.597T>C
 gnomAD v4
7g.152648910A>TCA370198398XRCC2c.407T>A (p.Phe136Tyr)
c.575T>A (p.Phe192Tyr)
n.597T>A
7g.152648911A=CA1753247076XRCC2c.406T= (p.Phe136=)
c.574T= (p.Phe192=)
n.596T=
7g.152648911A>CCA370198399XRCC2c.406T>G (p.Phe136Val)
c.574T>G (p.Phe192Val)
n.596T>G
7g.152648911A>GCA370198400XRCC2c.406T>C (p.Phe136Leu)
c.574T>C (p.Phe192Leu)
n.596T>C
 ClinVar dbSNP
7g.152648911A>TCA370198401XRCC2c.406T>A (p.Phe136Ile)
c.574T>A (p.Phe192Ile)
n.596T>A
7g.152648912A>CCA458895424XRCC2c.405T>G (p.Leu135=)
c.573T>G (p.Leu191=)
n.595T>G
7g.152648912A>GCA458895425XRCC2c.405T>C (p.Leu135=)
c.573T>C (p.Leu191=)
n.595T>C
7g.152648912A>TCA458895426XRCC2c.405T>A (p.Leu135=)
c.573T>A (p.Leu191=)
n.595T>A
7g.152648913A>CCA370198402XRCC2c.404T>G (p.Leu135Arg)
c.572T>G (p.Leu191Arg)
n.594T>G
7g.152648913A>GCA370198403XRCC2c.404T>C (p.Leu135Pro)
c.572T>C (p.Leu191Pro)
n.594T>C
7g.152648913A>TCA370198404XRCC2c.404T>A (p.Leu135His)
c.572T>A (p.Leu191His)
n.594T>A
7g.152648914G>ACA370198407XRCC2c.403C>T (p.Leu135Phe)
c.571C>T (p.Leu191Phe)
n.593C>T
7g.152648914G>CCA370198406XRCC2c.403C>G (p.Leu135Val)
c.571C>G (p.Leu191Val)
n.593C>G
7g.152648914G=CA1753247083XRCC2c.403C= (p.Leu135=)
c.571C= (p.Leu191=)
n.593C=
7g.152648914G>TCA370198405XRCC2c.403C>A (p.Leu135Ile)
c.571C>A (p.Leu191Ile)
n.593C>A
 ClinVar dbSNP COSMIC
7g.152648914_152648915delinsGACA1753247082XRCC2c.402_403delinsTC (p.Val134=)
c.570_571delinsTC (p.Val190=)
n.592_593delinsTC
7g.152648915A>CCA458895431XRCC2c.402T>G (p.Val134=)
c.570T>G (p.Val190=)
n.592T>G
7g.152648915A>GCA458895432XRCC2c.402T>C (p.Val134=)
c.570T>C (p.Val190=)
n.592T>C
7g.152648915A>TCA458895430XRCC2c.402T>A (p.Val134=)
c.570T>A (p.Val190=)
n.592T>A
7g.152648916delCA10584278XRCC2c.402del (p.Leu135PhefsTer8)
c.570del (p.Leu191PhefsTer8)
n.592del
 ClinVar dbSNP
7g.152648916A=CA1753247087XRCC2c.401T= (p.Val134=)
c.569T= (p.Val190=)
n.591T=
7g.152648916A>CCA370198410XRCC2c.401T>G (p.Val134Gly)
c.569T>G (p.Val190Gly)
n.591T>G
7g.152648916A>GCA370198408XRCC2c.401T>C (p.Val134Ala)
c.569T>C (p.Val190Ala)
n.591T>C
7g.152648916A>TCA370198409XRCC2c.401T>A (p.Val134Asp)
c.569T>A (p.Val190Asp)
n.591T>A
 ClinVar dbSNP
7g.152648917C>ACA370198411XRCC2c.400G>T (p.Val134Phe)
c.568G>T (p.Val190Phe)
n.590G>T
7g.152648917C>GCA370198412XRCC2c.400G>C (p.Val134Leu)
c.568G>C (p.Val190Leu)
n.590G>C
 dbSNP
7g.152648917C>TCA370198413XRCC2c.400G>A (p.Val134Ile)
c.568G>A (p.Val190Ile)
n.590G>A
 dbSNP
7g.152648918C>ACA458895433XRCC2c.399G>T (p.Leu133=)
c.567G>T (p.Leu189=)
n.589G>T
7g.152648918C>GCA458895434XRCC2c.399G>C (p.Leu133=)
c.567G>C (p.Leu189=)
n.589G>C
7g.152648918C>TCA458895435XRCC2c.399G>A (p.Leu133=)
c.567G>A (p.Leu189=)
n.589G>A
 ClinVar dbSNP
7g.152648919A>CCA370198414XRCC2c.398T>G (p.Leu133Arg)
c.566T>G (p.Leu189Arg)
n.588T>G
7g.152648919A>GCA370198415XRCC2c.398T>C (p.Leu133Pro)
c.566T>C (p.Leu189Pro)
n.588T>C
7g.152648919A>TCA370198416XRCC2c.398T>A (p.Leu133Gln)
c.566T>A (p.Leu189Gln)
n.588T>A
7g.152648920G>ACA458895439XRCC2c.397C>T (p.Leu133=)
c.565C>T (p.Leu189=)
n.587C>T
7g.152648920G>CCA370198417XRCC2c.397C>G (p.Leu133Val)
c.565C>G (p.Leu189Val)
n.587C>G
 ClinVar dbSNP
7g.152648920G=CA1753247093XRCC2c.397C= (p.Leu133=)
c.565C= (p.Leu189=)
n.587C=
7g.152648920G>TCA4582329XRCC2c.397C>A (p.Leu133Met)
c.565C>A (p.Leu189Met)
n.587C>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.152648920_152648922delinsTGTCA2580077741XRCC2c.395_397delinsACA (p.Arg132_Leu133delinsHisMet)
c.563_565delinsACA (p.Arg188_Leu189delinsHisMet)
n.585_587delinsACA
 ClinVar
7g.152648921G>ACA458895442XRCC2c.396C>T (p.Arg132=)
c.564C>T (p.Arg188=)
n.586C>T
 ClinVar gnomAD v4
7g.152648921G>CCA458895440XRCC2c.396C>G (p.Arg132=)
c.564C>G (p.Arg188=)
n.586C>G
 dbSNP
7g.152648921G>TCA458895441XRCC2c.396C>A (p.Arg132=)
c.564C>A (p.Arg188=)
n.586C>A
7g.152648921_152648922delinsAACA2580077742XRCC2c.395_396delinsTT (p.Arg132Leu)
c.563_564delinsTT (p.Arg188Leu)
n.585_586delinsTT
 ClinVar
7g.152648922C>ACA370198418XRCC2c.395G>T (p.Arg132Leu)
c.563G>T (p.Arg188Leu)
n.585G>T
 dbSNP gnomAD v4
7g.152648922C=CA1753247102XRCC2c.395G= (p.Arg132=)
c.563G= (p.Arg188=)
n.585G=
7g.152648922C>GCA370198419XRCC2c.395G>C (p.Arg132Pro)
c.563G>C (p.Arg188Pro)
n.585G>C
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.152648922C>TCA4582330XRCC2c.395G>A (p.Arg132His)
c.563G>A (p.Arg188His)
n.585G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648923G>ACA300473XRCC2c.394C>T (p.Arg132Cys)
c.562C>T (p.Arg188Cys)
n.584C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648923G>CCA370198421XRCC2c.394C>G (p.Arg132Gly)
c.562C>G (p.Arg188Gly)
n.584C>G
7g.152648923G=CA1753247110XRCC2c.394C= (p.Arg132=)
c.562C= (p.Arg188=)
n.584C=
7g.152648923G>TCA370198420XRCC2c.394C>A (p.Arg132Ser)
c.562C>A (p.Arg188Ser)
n.584C>A
 gnomAD v4
7g.152648924A=CA1753247115XRCC2c.393T= (p.Tyr131=)
c.561T= (p.Tyr187=)
n.583T=
7g.152648924A>CCA370198422XRCC2c.393T>G (p.Tyr131Ter)
c.561T>G (p.Tyr187Ter)
n.583T>G
7g.152648924A>GCA458895444XRCC2c.393T>C (p.Tyr131=)
c.561T>C (p.Tyr187=)
n.583T>C
7g.152648924A>TCA370198423XRCC2c.393T>A (p.Tyr131Ter)
c.561T>A (p.Tyr187Ter)
n.583T>A
7g.152648925T>ACA370198424XRCC2c.392A>T (p.Tyr131Phe)
c.560A>T (p.Tyr187Phe)
n.582A>T
7g.152648925T>CCA370198425XRCC2c.392A>G (p.Tyr131Cys)
c.560A>G (p.Tyr187Cys)
n.582A>G
 ClinVar dbSNP gnomAD v4
7g.152648925T>GCA370198426XRCC2c.392A>C (p.Tyr131Ser)
c.560A>C (p.Tyr187Ser)
n.582A>C
7g.152648925T=CA1753247118XRCC2c.392A= (p.Tyr131=)
c.560A= (p.Tyr187=)
n.582A=
7g.152648926A>CCA370198427XRCC2c.391T>G (p.Tyr131Asp)
c.559T>G (p.Tyr187Asp)
n.581T>G
 ClinVar gnomAD v4
7g.152648926A>GCA370198428XRCC2c.391T>C (p.Tyr131His)
c.559T>C (p.Tyr187His)
n.581T>C
7g.152648926A>TCA370198429XRCC2c.391T>A (p.Tyr131Asn)
c.559T>A (p.Tyr187Asn)
n.581T>A
7g.152648927G>ACA458895445XRCC2c.390C>T (p.Asp130=)
c.558C>T (p.Asp186=)
n.580C>T
7g.152648927G>CCA370198430XRCC2c.390C>G (p.Asp130Glu)
c.558C>G (p.Asp186Glu)
n.580C>G
 dbSNP
7g.152648927G>TCA370198431XRCC2c.390C>A (p.Asp130Glu)
c.558C>A (p.Asp186Glu)
n.580C>A
7g.152648928T>ACA370198433XRCC2c.389A>T (p.Asp130Val)
c.557A>T (p.Asp186Val)
n.579A>T
7g.152648928T>CCA370198434XRCC2c.389A>G (p.Asp130Gly)
c.557A>G (p.Asp186Gly)
n.579A>G
7g.152648928T>GCA370198432XRCC2c.389A>C (p.Asp130Ala)
c.557A>C (p.Asp186Ala)
n.579A>C
 gnomAD v4
7g.152648929C>ACA370198435XRCC2c.388G>T (p.Asp130Tyr)
c.556G>T (p.Asp186Tyr)
n.578G>T
 ClinVar dbSNP
7g.152648929C>GCA370198436XRCC2c.388G>C (p.Asp130His)
c.556G>C (p.Asp186His)
n.578G>C
 ClinVar
7g.152648929C>TCA370198437XRCC2c.388G>A (p.Asp130Asn)
c.556G>A (p.Asp186Asn)
n.578G>A
7g.152648930A>CCA370198438XRCC2c.387T>G (p.Asn129Lys)
c.555T>G (p.Asn185Lys)
n.577T>G
 ClinVar dbSNP
7g.152648930A>GCA458895447XRCC2c.387T>C (p.Asn129=)
c.555T>C (p.Asn185=)
n.577T>C
 dbSNP gnomAD v4
7g.152648930A>TCA370198439XRCC2c.387T>A (p.Asn129Lys)
c.555T>A (p.Asn185Lys)
n.577T>A
7g.152648931T>ACA370198442XRCC2c.386A>T (p.Asn129Ile)
c.554A>T (p.Asn185Ile)
n.576A>T
7g.152648931T>CCA370198441XRCC2c.386A>G (p.Asn129Ser)
c.554A>G (p.Asn185Ser)
n.576A>G
7g.152648931T>GCA370198440XRCC2c.386A>C (p.Asn129Thr)
c.554A>C (p.Asn185Thr)
n.576A>C
7g.152648932T>ACA370198443XRCC2c.385A>T (p.Asn129Tyr)
c.553A>T (p.Asn185Tyr)
n.575A>T
7g.152648932T>CCA370198444XRCC2c.385A>G (p.Asn129Asp)
c.553A>G (p.Asn185Asp)
n.575A>G
7g.152648932T>GCA370198445XRCC2c.385A>C (p.Asn129His)
c.553A>C (p.Asn185His)
n.575A>C
7g.152648933T>ACA458895448XRCC2c.384A>T (p.Val128=)
c.552A>T (p.Val184=)
n.574A>T
 ClinVar
7g.152648933T>CCA458895449XRCC2c.384A>G (p.Val128=)
c.552A>G (p.Val184=)
n.574A>G
 gnomAD v4
7g.152648933T>GCA458895450XRCC2c.384A>C (p.Val128=)
c.552A>C (p.Val184=)
n.574A>C
 ClinVar
7g.152648934A>CCA370198446XRCC2c.383T>G (p.Val128Gly)
c.551T>G (p.Val184Gly)
n.573T>G
7g.152648934A>GCA370198447XRCC2c.383T>C (p.Val128Ala)
c.551T>C (p.Val184Ala)
n.573T>C
7g.152648934A>TCA370198448XRCC2c.383T>A (p.Val128Glu)
c.551T>A (p.Val184Glu)
n.573T>A
7g.152648935C>ACA370198449XRCC2c.382G>T (p.Val128Leu)
c.550G>T (p.Val184Leu)
n.572G>T
7g.152648935C=CA1753247120XRCC2c.382G= (p.Val128=)
c.550G= (p.Val184=)
n.572G=
7g.152648935C>GCA370198451XRCC2c.382G>C (p.Val128Leu)
c.550G>C (p.Val184Leu)
n.572G>C
7g.152648935C>TCA370198450XRCC2c.382G>A (p.Val128Ile)
c.550G>A (p.Val184Ile)
n.572G>A
 ClinVar dbSNP gnomAD v4
7g.152648936A=CA1753247124XRCC2c.381T= (p.Leu127=)
c.549T= (p.Leu183=)
n.571T=
7g.152648936A>CCA458895452XRCC2c.381T>G (p.Leu127=)
c.549T>G (p.Leu183=)
n.571T>G
 ClinVar gnomAD v4
7g.152648936A>GCA458895453XRCC2c.381T>C (p.Leu127=)
c.549T>C (p.Leu183=)
n.571T>C
 ClinVar dbSNP
7g.152648936A>TCA458895454XRCC2c.381T>A (p.Leu127=)
c.549T>A (p.Leu183=)
n.571T>A
7g.152648937A>CCA370198452XRCC2c.380T>G (p.Leu127Arg)
c.548T>G (p.Leu183Arg)
n.570T>G
7g.152648937A>GCA370198453XRCC2c.380T>C (p.Leu127Pro)
c.548T>C (p.Leu183Pro)
n.570T>C
 ClinVar gnomAD v4
7g.152648937A>TCA370198454XRCC2c.380T>A (p.Leu127His)
c.548T>A (p.Leu183His)
n.570T>A
7g.152648938G>ACA370198455XRCC2c.379C>T (p.Leu127Phe)
c.547C>T (p.Leu183Phe)
n.569C>T
7g.152648938G>CCA370198456XRCC2c.379C>G (p.Leu127Val)
c.547C>G (p.Leu183Val)
n.569C>G
 dbSNP gnomAD v4
7g.152648938G>TCA370198457XRCC2c.379C>A (p.Leu127Ile)
c.547C>A (p.Leu183Ile)
n.569C>A
7g.152648939C>ACA370198458XRCC2c.378G>T (p.Lys126Asn)
c.546G>T (p.Lys182Asn)
n.568G>T
 ClinVar COSMIC
7g.152648939C=CA1753247128XRCC2c.378G= (p.Lys126=)
c.546G= (p.Lys182=)
n.568G=
7g.152648939C>GCA4582331XRCC2c.378G>C (p.Lys126Asn)
c.546G>C (p.Lys182Asn)
n.568G>C
 dbSNP ExAC gnomAD v2
7g.152648939C>TCA458895455XRCC2c.378G>A (p.Lys126=)
c.546G>A (p.Lys182=)
n.568G>A
7g.152648939_152648940delinsCTCA1753247127XRCC2c.377_378delinsAG (p.Lys126=)
c.545_546delinsAG (p.Lys182=)
n.567_568delinsAG
7g.152648940T>ACA370198459XRCC2c.377A>T (p.Lys126Met)
c.545A>T (p.Lys182Met)
n.567A>T
7g.152648940T>CCA370198460XRCC2c.377A>G (p.Lys126Arg)
c.545A>G (p.Lys182Arg)
n.567A>G
 gnomAD v4
7g.152648940T>GCA370198461XRCC2c.377A>C (p.Lys126Thr)
c.545A>C (p.Lys182Thr)
n.567A>C
 ClinVar
7g.152648941delCA288138XRCC2c.377del (p.Lys126SerfsTer3)
c.545del (p.Lys182SerfsTer3)
n.567del
 ClinVar dbSNP
7g.152648941T>ACA370198462XRCC2c.376A>T (p.Lys126Ter)
c.544A>T (p.Lys182Ter)
n.566A>T
 dbSNP
7g.152648941T>CCA16618429XRCC2c.376A>G (p.Lys126Glu)
c.544A>G (p.Lys182Glu)
n.566A>G
 ClinVar dbSNP gnomAD v4
7g.152648941T>GCA370198463XRCC2c.376A>C (p.Lys126Gln)
c.544A>C (p.Lys182Gln)
n.566A>C
7g.152648941T=CA1753247137XRCC2c.376A= (p.Lys126=)
c.544A= (p.Lys182=)
n.566A=
7g.152648942C>ACA370198464XRCC2c.375G>T (p.Glu125Asp)
c.543G>T (p.Glu181Asp)
n.565G>T
7g.152648942C>GCA370198465XRCC2c.375G>C (p.Glu125Asp)
c.543G>C (p.Glu181Asp)
n.565G>C
7g.152648942C>TCA458895456XRCC2c.375G>A (p.Glu125=)
c.543G>A (p.Glu181=)
n.565G>A
7g.152648943T>ACA370198466XRCC2c.374A>T (p.Glu125Val)
c.542A>T (p.Glu181Val)
n.564A>T
7g.152648943T>CCA370198468XRCC2c.374A>G (p.Glu125Gly)
c.542A>G (p.Glu181Gly)
n.564A>G
7g.152648943T>GCA370198467XRCC2c.374A>C (p.Glu125Ala)
c.542A>C (p.Glu181Ala)
n.564A>C
7g.152648944C>ACA370198469XRCC2c.373G>T (p.Glu125Ter)
c.541G>T (p.Glu181Ter)
n.563G>T
7g.152648944C>GCA370198471XRCC2c.373G>C (p.Glu125Gln)
c.541G>C (p.Glu181Gln)
n.563G>C
 ClinVar gnomAD v4 COSMIC
7g.152648944C>TCA370198470XRCC2c.373G>A (p.Glu125Lys)
c.541G>A (p.Glu181Lys)
n.563G>A
7g.152648945T>ACA370198472XRCC2c.372A>T (p.Leu124Phe)
c.540A>T (p.Leu180Phe)
n.562A>T
 ClinVar
7g.152648945T>CCA458895295XRCC2c.372A>G (p.Leu124=)
c.540A>G (p.Leu180=)
n.562A>G
7g.152648945T>GCA370198473XRCC2c.372A>C (p.Leu124Phe)
c.540A>C (p.Leu180Phe)
n.562A>C
7g.152648946A=CA1753247141XRCC2c.371T= (p.Leu124=)
c.539T= (p.Leu180=)
n.561T=
7g.152648946A>CCA370198474XRCC2c.371T>G (p.Leu124Ter)
c.539T>G (p.Leu180Ter)
n.561T>G
7g.152648946A>GCA370198475XRCC2c.371T>C (p.Leu124Ser)
c.539T>C (p.Leu180Ser)
n.561T>C
7g.152648946A>TCA16618430XRCC2c.371T>A (p.Leu124Ter)
c.539T>A (p.Leu180Ter)
n.561T>A
 ClinVar dbSNP gnomAD v4
7g.152648947A>CCA370198476XRCC2c.370T>G (p.Leu124Val)
c.538T>G (p.Leu180Val)
n.560T>G
7g.152648947A>GCA458895296XRCC2c.370T>C (p.Leu124=)
c.538T>C (p.Leu180=)
n.560T>C
7g.152648947A>TCA370198477XRCC2c.370T>A (p.Leu124Ile)
c.538T>A (p.Leu180Ile)
n.560T>A
7g.152648948G>ACA458895297XRCC2c.369C>T (p.Cys123=)
c.537C>T (p.Cys179=)
n.559C>T
 dbSNP
7g.152648948G>CCA370198478XRCC2c.369C>G (p.Cys123Trp)
c.537C>G (p.Cys179Trp)
n.559C>G
7g.152648948G>TCA370198479XRCC2c.369C>A (p.Cys123Ter)
c.537C>A (p.Cys179Ter)
n.559C>A

Number of alleles fetched