Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.152648831A>CCA370198239XRCC2c.486T>G (p.Asp162Glu)
c.654T>G (p.Asp218Glu)
n.676T>G
7g.152648831A>GCA458895325XRCC2c.486T>C (p.Asp162=)
c.654T>C (p.Asp218=)
n.676T>C
 ClinVar dbSNP gnomAD v4
7g.152648831A>TCA370198240XRCC2c.486T>A (p.Asp162Glu)
c.654T>A (p.Asp218Glu)
n.676T>A
7g.152648832T>ACA370198241XRCC2c.485A>T (p.Asp162Val)
c.653A>T (p.Asp218Val)
n.675A>T
7g.152648832T>CCA370198243XRCC2c.485A>G (p.Asp162Gly)
c.653A>G (p.Asp218Gly)
n.675A>G
 ClinVar dbSNP gnomAD v4
7g.152648832T>GCA370198242XRCC2c.485A>C (p.Asp162Ala)
c.653A>C (p.Asp218Ala)
n.675A>C
7g.152648832_152648834delinsTCACA1753246865XRCC2c.483_485delinsTGA (p.Cys161=)
c.651_653delinsTGA (p.Cys217=)
n.673_675delinsTGA
7g.152648833C>ACA370198244XRCC2c.484G>T (p.Asp162Tyr)
c.652G>T (p.Asp218Tyr)
n.674G>T
7g.152648833C=CA1753246872XRCC2c.484G= (p.Asp162=)
c.652G= (p.Asp218=)
n.674G=
7g.152648833C>GCA370198245XRCC2c.484G>C (p.Asp162His)
c.652G>C (p.Asp218His)
n.674G>C
7g.152648833C>TCA370198246XRCC2c.484G>A (p.Asp162Asn)
c.652G>A (p.Asp218Asn)
n.674G>A
 dbSNP gnomAD v2 gnomAD v4
7g.152648837_152648838delCA16618428XRCC2c.483_484del (p.Cys161Ter)
c.651_652del (p.Cys217Ter)
n.673_674del
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.152648834A=CA1753246876XRCC2c.483T= (p.Cys161=)
c.651T= (p.Cys217=)
n.673T=
7g.152648834A>CCA370198248XRCC2c.483T>G (p.Cys161Trp)
c.651T>G (p.Cys217Trp)
n.673T>G
7g.152648834A>GCA458895327XRCC2c.483T>C (p.Cys161=)
c.651T>C (p.Cys217=)
n.673T>C
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.152648834A>TCA370198247XRCC2c.483T>A (p.Cys161Ter)
c.651T>A (p.Cys217Ter)
n.673T>A
7g.152648838_152648839insACCAAACACACCCAACACACA2778474372XRCC2c.483_484insTGGGTGTGTTTGGTTGTGT (p.Asp162TrpfsTer7)
c.651_652insTGGGTGTGTTTGGTTGTGT (p.Asp218TrpfsTer7)
n.673_674insTGGGTGTGTTTGGTTGTGT
7g.152648835C>ACA370198249XRCC2c.482G>T (p.Cys161Phe)
c.650G>T (p.Cys217Phe)
n.672G>T
7g.152648835C=CA1753246879XRCC2c.482G= (p.Cys161=)
c.650G= (p.Cys217=)
n.672G=
7g.152648835C>GCA370198250XRCC2c.482G>C (p.Cys161Ser)
c.650G>C (p.Cys217Ser)
n.672G>C
 dbSNP
7g.152648835C>TCA10584276XRCC2c.482G>A (p.Cys161Tyr)
c.650G>A (p.Cys217Tyr)
n.672G>A
 ClinVar dbSNP
7g.152648836A=CA1753246882XRCC2c.481T= (p.Cys161=)
c.649T= (p.Cys217=)
n.671T=
7g.152648836A>CCA370198251XRCC2c.481T>G (p.Cys161Gly)
c.649T>G (p.Cys217Gly)
n.671T>G
7g.152648836A>GCA370198252XRCC2c.481T>C (p.Cys161Arg)
c.649T>C (p.Cys217Arg)
n.671T>C
 dbSNP
7g.152648836A>TCA370198253XRCC2c.481T>A (p.Cys161Ser)
c.649T>A (p.Cys217Ser)
n.671T>A
 gnomAD v4
7g.152648837C>ACA458895330XRCC2c.480G>T (p.Leu160=)
c.648G>T (p.Leu216=)
n.670G>T
 ClinVar
7g.152648837C>GCA458895331XRCC2c.480G>C (p.Leu160=)
c.648G>C (p.Leu216=)
n.670G>C
7g.152648837C>TCA458895332XRCC2c.480G>A (p.Leu160=)
c.648G>A (p.Leu216=)
n.670G>A
 ClinVar gnomAD v4
7g.152648837_152648847delinsCAGTCGTCGAGCA1753246884XRCC2c.470_480delinsCTCGACGACTG (p.Ser157=)
c.638_648delinsCTCGACGACTG (p.Ser213=)
n.660_670delinsCTCGACGACTG
7g.152648838A=CA1753246887XRCC2c.479T= (p.Leu160=)
c.647T= (p.Leu216=)
n.669T=
7g.152648838A>CCA370198254XRCC2c.479T>G (p.Leu160Arg)
c.647T>G (p.Leu216Arg)
n.669T>G
7g.152648838A>GCA370198255XRCC2c.479T>C (p.Leu160Pro)
c.647T>C (p.Leu216Pro)
n.669T>C
 ClinVar dbSNP gnomAD v4
7g.152648838A>TCA370198256XRCC2c.479T>A (p.Leu160Gln)
c.647T>A (p.Leu216Gln)
n.669T>A
7g.152648840_152648849delCA579080840XRCC2c.470_479del (p.Ser157CysfsTer6)
c.638_647del (p.Ser213CysfsTer6)
n.660_669del
 dbSNP gnomAD v2 gnomAD v4
7g.152648839G>ACA458895333XRCC2c.478C>T (p.Leu160=)
c.646C>T (p.Leu216=)
n.668C>T
7g.152648839G>CCA370198257XRCC2c.478C>G (p.Leu160Val)
c.646C>G (p.Leu216Val)
n.668C>G
 dbSNP
7g.152648839G>TCA370198258XRCC2c.478C>A (p.Leu160Met)
c.646C>A (p.Leu216Met)
n.668C>A
7g.152648840T>ACA458895335XRCC2c.477A>T (p.Arg159=)
c.645A>T (p.Arg215=)
n.667A>T
7g.152648840T>CCA458895336XRCC2c.477A>G (p.Arg159=)
c.645A>G (p.Arg215=)
n.667A>G
 gnomAD v4
7g.152648840T>GCA458895337XRCC2c.477A>C (p.Arg159=)
c.645A>C (p.Arg215=)
n.667A>C
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.152648840T=CA1753246889XRCC2c.477A= (p.Arg159=)
c.645A= (p.Arg215=)
n.667A=
7g.152648841C>ACA370198260XRCC2c.476G>T (p.Arg159Leu)
c.644G>T (p.Arg215Leu)
n.666G>T
 gnomAD v4
7g.152648841C=CA1753246892XRCC2c.476G= (p.Arg159=)
c.644G= (p.Arg215=)
n.666G=
7g.152648841C>GCA370198259XRCC2c.476G>C (p.Arg159Pro)
c.644G>C (p.Arg215Pro)
n.666G>C
7g.152648841C>TCA4582316XRCC2c.476G>A (p.Arg159Gln)
c.644G>A (p.Arg215Gln)
n.666G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.152648842G>ACA128903XRCC2c.475C>T (p.Arg159Ter)
c.643C>T (p.Arg215Ter)
n.665C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.152648842G>CCA370198261XRCC2c.475C>G (p.Arg159Gly)
c.643C>G (p.Arg215Gly)
n.665C>G
7g.152648842G=CA1753246897XRCC2c.475C= (p.Arg159=)
c.643C= (p.Arg215=)
n.665C=
7g.152648842G>TCA458895338XRCC2c.475C>A (p.Arg159=)
c.643C>A (p.Arg215=)
n.665C>A
 gnomAD v4
7g.152648843T>ACA458895340XRCC2c.474A>T (p.Arg158=)
c.642A>T (p.Arg214=)
n.664A>T
 dbSNP

Number of alleles fetched