Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.58692654delCA913013104RAD51Cc.11del (p.Lys4ArgfsTer12)
n.82del
c.-238del (p.=)
c.-207+22del (p.=)
c.-538del (p.=)
c.-699del (p.=)
n.84del
c.-512del (p.=)
n.515del
n.53del
n.57+22del
17g.58692654A>CCA400336133RAD51Cc.11A>C (p.Lys4Thr)
n.82A>C
c.-238A>C (p.=)
c.-207+22A>C (p.=)
c.-538A>C (p.=)
c.-699A>C (p.=)
n.84A>C
c.-512A>C (p.=)
n.515A>C
n.53A>C
n.57+22A>C
17g.58692654A>GCA400336138RAD51Cc.11A>G (p.Lys4Arg)
n.82A>G
c.-238A>G (p.=)
c.-207+22A>G (p.=)
c.-538A>G (p.=)
c.-699A>G (p.=)
n.84A>G
c.-512A>G (p.=)
n.515A>G
n.53A>G
n.57+22A>G
17g.58692654A>TCA400336141RAD51Cc.11A>T (p.Lys4Met)
n.82A>T
c.-238A>T (p.=)
c.-207+22A>T (p.=)
c.-538A>T (p.=)
c.-699A>T (p.=)
n.84A>T
c.-512A>T (p.=)
n.515A>T
n.53A>T
n.57+22A>T
17g.58692655G>ACA8677118RAD51Cc.12G>A (p.Lys4=)
n.83G>A
c.-237G>A (p.=)
c.-207+23G>A (p.=)
c.-537G>A (p.=)
c.-698G>A (p.=)
n.85G>A
c.-511G>A (p.=)
n.516G>A
n.54G>A
n.57+23G>A
ClinVar dbSNP ExAC gnomAD COSMIC COSMIC
17g.58692655G>CCA400336144RAD51Cc.12G>C (p.Lys4Asn)
n.83G>C
c.-237G>C (p.=)
c.-207+23G>C (p.=)
c.-537G>C (p.=)
c.-698G>C (p.=)
n.85G>C
c.-511G>C (p.=)
n.516G>C
n.54G>C
n.57+23G>C
17g.58692655G>TCA400336142RAD51Cc.12G>T (p.Lys4Asn)
n.83G>T
c.-237G>T (p.=)
c.-207+23G>T (p.=)
c.-537G>T (p.=)
c.-698G>T (p.=)
n.85G>T
c.-511G>T (p.=)
n.516G>T
n.54G>T
n.57+23G>T
17g.58692656A>CCA400336150RAD51Cc.13A>C (p.Thr5Pro)
n.84A>C
c.-236A>C (p.=)
c.-207+24A>C (p.=)
c.-536A>C (p.=)
c.-697A>C (p.=)
n.86A>C
c.-510A>C (p.=)
n.517A>C
n.55A>C
n.57+24A>C
gnomAD
17g.58692656A>GCA400336151RAD51Cc.13A>G (p.Thr5Ala)
n.84A>G
c.-236A>G (p.=)
c.-207+24A>G (p.=)
c.-536A>G (p.=)
c.-697A>G (p.=)
n.86A>G
c.-510A>G (p.=)
n.517A>G
n.55A>G
n.57+24A>G
17g.58692656A>TCA400336152RAD51Cc.13A>T (p.Thr5Ser)
n.84A>T
c.-236A>T (p.=)
c.-207+24A>T (p.=)
c.-536A>T (p.=)
c.-697A>T (p.=)
n.86A>T
c.-510A>T (p.=)
n.517A>T
n.55A>T
n.57+24A>T
gnomAD
17g.58692657C>ACA400336153RAD51Cc.14C>A (p.Thr5Lys)
n.85C>A
c.-235C>A (p.=)
c.-207+25C>A (p.=)
c.-535C>A (p.=)
c.-696C>A (p.=)
n.87C>A
c.-509C>A (p.=)
n.518C>A
n.56C>A
n.57+25C>A
17g.58692657C>GCA8677119RAD51Cc.14C>G (p.Thr5Arg)
n.85C>G
c.-235C>G (p.=)
c.-207+25C>G (p.=)
c.-535C>G (p.=)
c.-696C>G (p.=)
n.87C>G
c.-509C>G (p.=)
n.518C>G
n.56C>G
n.57+25C>G
ClinVar dbSNP ExAC gnomAD
17g.58692657C>TCA288621RAD51Cc.14C>T (p.Thr5Met)
n.85C>T
c.-235C>T (p.=)
c.-207+25C>T (p.=)
c.-535C>T (p.=)
c.-696C>T (p.=)
n.87C>T
c.-509C>T (p.=)
n.518C>T
n.56C>T
n.57+25C>T
ClinVar dbSNP ExAC gnomAD
17g.58692658G>ACA501074326RAD51Cc.15G>A (p.Thr5=)
n.86G>A
c.-234G>A (p.=)
c.-207+26G>A (p.=)
c.-534G>A (p.=)
c.-695G>A (p.=)
n.88G>A
c.-508G>A (p.=)
n.519G>A
n.57G>A
n.57+26G>A
17g.58692658G>CCA8677120RAD51Cc.15G>C (p.Thr5=)
n.86G>C
c.-234G>C (p.=)
c.-207+26G>C (p.=)
c.-534G>C (p.=)
c.-695G>C (p.=)
n.88G>C
c.-508G>C (p.=)
n.519G>C
n.57G>C
n.57+26G>C
dbSNP ExAC gnomAD
17g.58692658G>TCA501074327RAD51Cc.15G>T (p.Thr5=)
n.86G>T
c.-234G>T (p.=)
c.-207+26G>T (p.=)
c.-534G>T (p.=)
c.-695G>T (p.=)
n.88G>T
c.-508G>T (p.=)
n.519G>T
n.57G>T
n.57+26G>T
gnomAD
17g.58692659T>ACA400336197RAD51Cc.16T>A (p.Phe6Ile)
n.87T>A
c.-233T>A (p.=)
c.-207+27T>A (p.=)
c.-533T>A (p.=)
c.-694T>A (p.=)
n.89T>A
c.-507T>A (p.=)
n.520T>A
n.58T>A
n.57+27T>A
17g.58692659T>CCA8677121RAD51Cc.16T>C (p.Phe6Leu)
n.87T>C
c.-233T>C (p.=)
c.-207+27T>C (p.=)
c.-533T>C (p.=)
c.-694T>C (p.=)
n.89T>C
c.-507T>C (p.=)
n.520T>C
n.58T>C
n.57+27T>C
dbSNP ExAC gnomAD
17g.58692659T>GCA400336210RAD51Cc.16T>G (p.Phe6Val)
n.87T>G
c.-233T>G (p.=)
c.-207+27T>G (p.=)
c.-533T>G (p.=)
c.-694T>G (p.=)
n.89T>G
c.-507T>G (p.=)
n.520T>G
n.58T>G
n.57+27T>G
ClinVar
17g.58692660T>ACA8677122RAD51Cc.17T>A (p.Phe6Tyr)
n.88T>A
c.-232T>A (p.=)
c.-207+28T>A (p.=)
c.-532T>A (p.=)
c.-693T>A (p.=)
n.90T>A
c.-506T>A (p.=)
n.521T>A
n.59T>A
n.57+28T>A
ClinVar dbSNP ExAC gnomAD
17g.58692660T>CCA400336219RAD51Cc.17T>C (p.Phe6Ser)
n.88T>C
c.-232T>C (p.=)
c.-207+28T>C (p.=)
c.-532T>C (p.=)
c.-693T>C (p.=)
n.90T>C
c.-506T>C (p.=)
n.521T>C
n.59T>C
n.57+28T>C
17g.58692660T>GCA400336224RAD51Cc.17T>G (p.Phe6Cys)
n.88T>G
c.-232T>G (p.=)
c.-207+28T>G (p.=)
c.-532T>G (p.=)
c.-693T>G (p.=)
n.90T>G
c.-506T>G (p.=)
n.521T>G
n.59T>G
n.57+28T>G
17g.58692661C>ACA400336231RAD51Cc.18C>A (p.Phe6Leu)
n.89C>A
c.-231C>A (p.=)
c.-207+29C>A (p.=)
c.-531C>A (p.=)
c.-692C>A (p.=)
n.91C>A
c.-505C>A (p.=)
n.522C>A
n.60C>A
n.57+29C>A
ClinVar
17g.58692661C>GCA400336227RAD51Cc.18C>G (p.Phe6Leu)
n.89C>G
c.-231C>G (p.=)
c.-207+29C>G (p.=)
c.-531C>G (p.=)
c.-692C>G (p.=)
n.91C>G
c.-505C>G (p.=)
n.522C>G
n.60C>G
n.57+29C>G
17g.58692661C>TCA8677123RAD51Cc.18C>T (p.Phe6=)
n.89C>T
c.-231C>T (p.=)
c.-207+29C>T (p.=)
c.-531C>T (p.=)
c.-692C>T (p.=)
n.91C>T
c.-505C>T (p.=)
n.522C>T
n.60C>T
n.57+29C>T
ClinVar dbSNP ExAC gnomAD
17g.58692662C>ACA400336232RAD51Cc.19C>A (p.Arg7Ser)
n.90C>A
c.-230C>A (p.=)
c.-207+30C>A (p.=)
c.-530C>A (p.=)
c.-691C>A (p.=)
n.92C>A
c.-504C>A (p.=)
n.523C>A
n.61C>A
n.57+30C>A
ClinVar gnomAD
17g.58692662C>GCA8677124RAD51Cc.19C>G (p.Arg7Gly)
n.90C>G
c.-230C>G (p.=)
c.-207+30C>G (p.=)
c.-530C>G (p.=)
c.-691C>G (p.=)
n.92C>G
c.-504C>G (p.=)
n.523C>G
n.61C>G
n.57+30C>G
ClinVar dbSNP ExAC gnomAD
17g.58692662C>TCA400336236RAD51Cc.19C>T (p.Arg7Cys)
n.90C>T
c.-230C>T (p.=)
c.-207+30C>T (p.=)
c.-530C>T (p.=)
c.-691C>T (p.=)
n.92C>T
c.-504C>T (p.=)
n.523C>T
n.61C>T
n.57+30C>T
ClinVar gnomAD
17g.58692663G>ACA292046832RAD51Cc.20G>A (p.Arg7His)
n.91G>A
c.-229G>A (p.=)
c.-207+31G>A (p.=)
c.-529G>A (p.=)
c.-690G>A (p.=)
n.93G>A
c.-503G>A (p.=)
n.524G>A
n.62G>A
n.57+31G>A
n.1G>A
ClinVar dbSNP
17g.58692663G>CCA400336247RAD51Cc.20G>C (p.Arg7Pro)
n.91G>C
c.-229G>C (p.=)
c.-207+31G>C (p.=)
c.-529G>C (p.=)
c.-690G>C (p.=)
n.93G>C
c.-503G>C (p.=)
n.524G>C
n.62G>C
n.57+31G>C
n.1G>C
ClinVar
17g.58692663G>TCA400336251RAD51Cc.20G>T (p.Arg7Leu)
n.91G>T
c.-229G>T (p.=)
c.-207+31G>T (p.=)
c.-529G>T (p.=)
c.-690G>T (p.=)
n.93G>T
c.-503G>T (p.=)
n.524G>T
n.62G>T
n.57+31G>T
n.1G>T
17g.58692664C>ACA501074329RAD51Cc.21C>A (p.Arg7=)
n.92C>A
c.-228C>A (p.=)
c.-207+32C>A (p.=)
c.-528C>A (p.=)
c.-689C>A (p.=)
n.94C>A
c.-502C>A (p.=)
n.525C>A
n.63C>A
n.57+32C>A
n.2C>A
ClinVar
17g.58692664C>GCA501074330RAD51Cc.21C>G (p.Arg7=)
n.92C>G
c.-228C>G (p.=)
c.-207+32C>G (p.=)
c.-528C>G (p.=)
c.-689C>G (p.=)
n.94C>G
c.-502C>G (p.=)
n.525C>G
n.63C>G
n.57+32C>G
n.2C>G
17g.58692664C>TCA501074331RAD51Cc.21C>T (p.Arg7=)
n.92C>T
c.-228C>T (p.=)
c.-207+32C>T (p.=)
c.-528C>T (p.=)
c.-689C>T (p.=)
n.94C>T
c.-502C>T (p.=)
n.525C>T
n.63C>T
n.57+32C>T
n.2C>T
ClinVar
17g.58692665T>ACA400336256RAD51Cc.22T>A (p.Phe8Ile)
n.93T>A
c.-227T>A (p.=)
c.-207+33T>A (p.=)
c.-527T>A (p.=)
c.-688T>A (p.=)
n.95T>A
c.-501T>A (p.=)
n.526T>A
n.64T>A
n.57+33T>A
n.3T>A
gnomAD
17g.58692665T>CCA400336259RAD51Cc.22T>C (p.Phe8Leu)
n.93T>C
c.-227T>C (p.=)
c.-207+33T>C (p.=)
c.-527T>C (p.=)
c.-688T>C (p.=)
n.95T>C
c.-501T>C (p.=)
n.526T>C
n.64T>C
n.57+33T>C
n.3T>C
17g.58692665T>GCA400336267RAD51Cc.22T>G (p.Phe8Val)
n.93T>G
c.-227T>G (p.=)
c.-207+33T>G (p.=)
c.-527T>G (p.=)
c.-688T>G (p.=)
n.95T>G
c.-501T>G (p.=)
n.526T>G
n.64T>G
n.57+33T>G
n.3T>G
17g.58692666T>ACA400336272RAD51Cc.23T>A (p.Phe8Tyr)
n.94T>A
c.-226T>A (p.=)
c.-207+34T>A (p.=)
c.-526T>A (p.=)
c.-687T>A (p.=)
n.96T>A
c.-500T>A (p.=)
n.527T>A
n.65T>A
n.57+34T>A
n.4T>A
17g.58692666T>CCA400336278RAD51Cc.23T>C (p.Phe8Ser)
n.94T>C
c.-226T>C (p.=)
c.-207+34T>C (p.=)
c.-526T>C (p.=)
c.-687T>C (p.=)
n.96T>C
c.-500T>C (p.=)
n.527T>C
n.65T>C
n.57+34T>C
n.4T>C
17g.58692666T>GCA400336282RAD51Cc.23T>G (p.Phe8Cys)
n.94T>G
c.-226T>G (p.=)
c.-207+34T>G (p.=)
c.-526T>G (p.=)
c.-687T>G (p.=)
n.96T>G
c.-500T>G (p.=)
n.527T>G
n.65T>G
n.57+34T>G
n.4T>G
17g.58692667T>ACA169336RAD51Cc.24T>A (p.Phe8Leu)
n.95T>A
c.-225T>A (p.=)
c.-207+35T>A (p.=)
c.-525T>A (p.=)
c.-686T>A (p.=)
n.97T>A
c.-499T>A (p.=)
n.528T>A
n.66T>A
n.57+35T>A
n.5T>A
ClinVar dbSNP
17g.58692667T>CCA501074332RAD51Cc.24T>C (p.Phe8=)
n.95T>C
c.-225T>C (p.=)
c.-207+35T>C (p.=)
c.-525T>C (p.=)
c.-686T>C (p.=)
n.97T>C
c.-499T>C (p.=)
n.528T>C
n.66T>C
n.57+35T>C
n.5T>C
17g.58692667T>GCA400336297RAD51Cc.24T>G (p.Phe8Leu)
n.95T>G
c.-225T>G (p.=)
c.-207+35T>G (p.=)
c.-525T>G (p.=)
c.-686T>G (p.=)
n.97T>G
c.-499T>G (p.=)
n.528T>G
n.66T>G
n.57+35T>G
n.5T>G
17g.58692668G>ACA400336327RAD51Cc.25G>A (p.Glu9Lys)
n.96G>A
c.-224G>A (p.=)
c.-207+36G>A (p.=)
c.-524G>A (p.=)
c.-685G>A (p.=)
n.98G>A
c.-498G>A (p.=)
n.529G>A
n.67G>A
n.57+36G>A
n.6G>A
17g.58692668G>CCA400336329RAD51Cc.25G>C (p.Glu9Gln)
n.96G>C
c.-224G>C (p.=)
c.-207+36G>C (p.=)
c.-524G>C (p.=)
c.-685G>C (p.=)
n.98G>C
c.-498G>C (p.=)
n.529G>C
n.67G>C
n.57+36G>C
n.6G>C
ClinVar
17g.58692668G>TCA400336331RAD51Cc.25G>T (p.Glu9Ter)
n.96G>T
c.-224G>T (p.=)
c.-207+36G>T (p.=)
c.-524G>T (p.=)
c.-685G>T (p.=)
n.98G>T
c.-498G>T (p.=)
n.529G>T
n.67G>T
n.57+36G>T
n.6G>T
17g.58692669A>CCA400336335RAD51Cc.26A>C (p.Glu9Ala)
n.97A>C
c.-223A>C (p.=)
c.-207+37A>C (p.=)
c.-523A>C (p.=)
c.-684A>C (p.=)
n.99A>C
c.-497A>C (p.=)
n.530A>C
n.68A>C
n.57+37A>C
n.7A>C
17g.58692669A>GCA400336344RAD51Cc.26A>G (p.Glu9Gly)
n.97A>G
c.-223A>G (p.=)
c.-207+37A>G (p.=)
c.-523A>G (p.=)
c.-684A>G (p.=)
n.99A>G
c.-497A>G (p.=)
n.530A>G
n.68A>G
n.57+37A>G
n.7A>G
17g.58692669A>TCA400336345RAD51Cc.26A>T (p.Glu9Val)
n.97A>T
c.-223A>T (p.=)
c.-207+37A>T (p.=)
c.-523A>T (p.=)
c.-684A>T (p.=)
n.99A>T
c.-497A>T (p.=)
n.530A>T
n.68A>T
n.57+37A>T
n.7A>T
17g.58692671delCA915950639RAD51Cc.28del (p.Met10CysfsTer6)
n.99del
c.-221del (p.=)
c.-207+39del (p.=)
c.-521del (p.=)
c.-682del (p.=)
n.101del
c.-495del (p.=)
n.532del
n.70del
n.57+39del
n.9del
ClinVar dbSNP

Number of alleles fetched