Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.58692640T>ACA658684132RAD51Cc.-4T>A (p.=)
n.68T>A
c.-252T>A (p.=)
c.-207+8T>A (p.=)
c.-552T>A (p.=)
c.-713T>A (p.=)
n.70T>A
c.-526T>A (p.=)
n.501T>A
n.39T>A
n.57+8T>A
 ClinVar
17g.58692641G>ACA349014RAD51Cc.-3G>A (p.=)
n.69G>A
c.-251G>A (p.=)
c.-207+9G>A (p.=)
c.-551G>A (p.=)
c.-712G>A (p.=)
n.71G>A
c.-525G>A (p.=)
n.502G>A
n.40G>A
n.57+9G>A
 ClinVar dbSNP
17g.58692641G>TCA915950638RAD51Cc.-3G>T (p.=)
n.69G>T
c.-251G>T (p.=)
c.-207+9G>T (p.=)
c.-551G>T (p.=)
c.-712G>T (p.=)
n.71G>T
c.-525G>T (p.=)
n.502G>T
n.40G>T
n.57+9G>T
 ClinVar
17g.58692642C>ACA292046768RAD51Cc.-2C>A (p.=)
n.70C>A
c.-250C>A (p.=)
c.-207+10C>A (p.=)
c.-550C>A (p.=)
c.-711C>A (p.=)
n.72C>A
c.-524C>A (p.=)
n.503C>A
n.41C>A
n.57+10C>A
 dbSNP
17g.58692642C>TCA10580717RAD51Cc.-2C>T (p.=)
n.70C>T
c.-250C>T (p.=)
c.-207+10C>T (p.=)
c.-550C>T (p.=)
c.-711C>T (p.=)
n.72C>T
c.-524C>T (p.=)
n.503C>T
n.41C>T
n.57+10C>T
 ClinVar dbSNP
17g.58692643G>ACA658684133RAD51Cc.-1G>A (p.=)
n.71G>A
c.-249G>A (p.=)
c.-207+11G>A (p.=)
c.-549G>A (p.=)
c.-710G>A (p.=)
n.73G>A
c.-523G>A (p.=)
n.504G>A
n.42G>A
n.57+11G>A
 ClinVar
17g.58692643G>TCA8677115RAD51Cc.-1G>T (p.=)
n.71G>T
c.-249G>T (p.=)
c.-207+11G>T (p.=)
c.-549G>T (p.=)
c.-710G>T (p.=)
n.73G>T
c.-523G>T (p.=)
n.504G>T
n.42G>T
n.57+11G>T
 dbSNP ExAC gnomAD
17g.58692644A>CCA400336035RAD51Cc.1A>C
n.72A>C
c.-248A>C (p.=)
c.-207+12A>C (p.=)
c.-548A>C (p.=)
c.-709A>C (p.=)
n.74A>C
c.-522A>C (p.=)
n.505A>C
n.43A>C
n.57+12A>C
17g.58692644A>GCA292046776RAD51Cc.1A>G
n.72A>G
c.-248A>G (p.=)
c.-207+12A>G (p.=)
c.-548A>G (p.=)
c.-709A>G (p.=)
n.74A>G
c.-522A>G (p.=)
n.505A>G
n.43A>G
n.57+12A>G
 ClinVar dbSNP
17g.58692644A>TCA400336042RAD51Cc.1A>T
n.72A>T
c.-248A>T (p.=)
c.-207+12A>T (p.=)
c.-548A>T (p.=)
c.-709A>T (p.=)
n.74A>T
c.-522A>T (p.=)
n.505A>T
n.43A>T
n.57+12A>T
 ClinVar
17g.58692645T>ACA400336047RAD51Cc.2T>A
n.73T>A
c.-247T>A (p.=)
c.-207+13T>A (p.=)
c.-547T>A (p.=)
c.-708T>A (p.=)
n.75T>A
c.-521T>A (p.=)
n.506T>A
n.44T>A
n.57+13T>A
17g.58692645T>CCA400336049RAD51Cc.2T>C
n.73T>C
c.-247T>C (p.=)
c.-207+13T>C (p.=)
c.-547T>C (p.=)
c.-708T>C (p.=)
n.75T>C
c.-521T>C (p.=)
n.506T>C
n.44T>C
n.57+13T>C
17g.58692645T>GCA400336057RAD51Cc.2T>G
n.73T>G
c.-247T>G (p.=)
c.-207+13T>G (p.=)
c.-547T>G (p.=)
c.-708T>G (p.=)
n.75T>G
c.-521T>G (p.=)
n.506T>G
n.44T>G
n.57+13T>G
17g.58692646G>ACA10580718RAD51Cc.3G>A
n.74G>A
c.-246G>A (p.=)
c.-207+14G>A (p.=)
c.-546G>A (p.=)
c.-707G>A (p.=)
n.76G>A
c.-520G>A (p.=)
n.507G>A
n.45G>A
n.57+14G>A
 ClinVar dbSNP gnomAD
17g.58692646G>CCA400336063RAD51Cc.3G>C
n.74G>C
c.-246G>C (p.=)
c.-207+14G>C (p.=)
c.-546G>C (p.=)
c.-707G>C (p.=)
n.76G>C
c.-520G>C (p.=)
n.507G>C
n.45G>C
n.57+14G>C
17g.58692646G>TCA337230RAD51Cc.3G>T
n.74G>T
c.-246G>T (p.=)
c.-207+14G>T (p.=)
c.-546G>T (p.=)
c.-707G>T (p.=)
n.76G>T
c.-520G>T (p.=)
n.507G>T
n.45G>T
n.57+14G>T
 ClinVar dbSNP
17g.58692647C>ACA400336068RAD51Cc.4C>A (p.Arg2Ser)
n.75C>A
c.-245C>A (p.=)
c.-207+15C>A (p.=)
c.-545C>A (p.=)
c.-706C>A (p.=)
n.77C>A
c.-519C>A (p.=)
n.508C>A
n.46C>A
n.57+15C>A
 gnomAD
17g.58692647C>GCA400336071RAD51Cc.4C>G (p.Arg2Gly)
n.75C>G
c.-245C>G (p.=)
c.-207+15C>G (p.=)
c.-545C>G (p.=)
c.-706C>G (p.=)
n.77C>G
c.-519C>G (p.=)
n.508C>G
n.46C>G
n.57+15C>G
 ClinVar gnomAD
17g.58692647C>TCA8677116RAD51Cc.4C>T (p.Arg2Cys)
n.75C>T
c.-245C>T (p.=)
c.-207+15C>T (p.=)
c.-545C>T (p.=)
c.-706C>T (p.=)
n.77C>T
c.-519C>T (p.=)
n.508C>T
n.46C>T
n.57+15C>T
 dbSNP ExAC gnomAD
17g.58692648G>ACA400336079RAD51Cc.5G>A (p.Arg2His)
n.76G>A
c.-244G>A (p.=)
c.-207+16G>A (p.=)
c.-544G>A (p.=)
c.-705G>A (p.=)
n.78G>A
c.-518G>A (p.=)
n.509G>A
n.47G>A
n.57+16G>A
17g.58692648G>CCA400336084RAD51Cc.5G>C (p.Arg2Pro)
n.76G>C
c.-244G>C (p.=)
c.-207+16G>C (p.=)
c.-544G>C (p.=)
c.-705G>C (p.=)
n.78G>C
c.-518G>C (p.=)
n.509G>C
n.47G>C
n.57+16G>C
17g.58692648G>TCA400336090RAD51Cc.5G>T (p.Arg2Leu)
n.76G>T
c.-244G>T (p.=)
c.-207+16G>T (p.=)
c.-544G>T (p.=)
c.-705G>T (p.=)
n.78G>T
c.-518G>T (p.=)
n.509G>T
n.47G>T
n.57+16G>T
17g.58692649C>ACA501074322RAD51Cc.6C>A (p.Arg2=)
n.77C>A
c.-243C>A (p.=)
c.-207+17C>A (p.=)
c.-543C>A (p.=)
c.-704C>A (p.=)
n.79C>A
c.-517C>A (p.=)
n.510C>A
n.48C>A
n.57+17C>A
17g.58692649C>GCA501074324RAD51Cc.6C>G (p.Arg2=)
n.77C>G
c.-243C>G (p.=)
c.-207+17C>G (p.=)
c.-543C>G (p.=)
c.-704C>G (p.=)
n.79C>G
c.-517C>G (p.=)
n.510C>G
n.48C>G
n.57+17C>G
 ClinVar
17g.58692649C>TCA501074323RAD51Cc.6C>T (p.Arg2=)
n.77C>T
c.-243C>T (p.=)
c.-207+17C>T (p.=)
c.-543C>T (p.=)
c.-704C>T (p.=)
n.79C>T
c.-517C>T (p.=)
n.510C>T
n.48C>T
n.57+17C>T
 ClinVar gnomAD
17g.58692650G>ACA188884RAD51Cc.7G>A (p.Gly3Arg)
n.78G>A
c.-242G>A (p.=)
c.-207+18G>A (p.=)
c.-542G>A (p.=)
c.-703G>A (p.=)
n.80G>A
c.-516G>A (p.=)
n.511G>A
n.49G>A
n.57+18G>A
 ClinVar dbSNP ExAC gnomAD
17g.58692650G>CCA400336093RAD51Cc.7G>C (p.Gly3Arg)
n.78G>C
c.-242G>C (p.=)
c.-207+18G>C (p.=)
c.-542G>C (p.=)
c.-703G>C (p.=)
n.80G>C
c.-516G>C (p.=)
n.511G>C
n.49G>C
n.57+18G>C
17g.58692650G>TCA400336094RAD51Cc.7G>T (p.Gly3Trp)
n.78G>T
c.-242G>T (p.=)
c.-207+18G>T (p.=)
c.-542G>T (p.=)
c.-703G>T (p.=)
n.80G>T
c.-516G>T (p.=)
n.511G>T
n.49G>T
n.57+18G>T
17g.58692651G>ACA400336095RAD51Cc.8G>A (p.Gly3Glu)
n.79G>A
c.-241G>A (p.=)
c.-207+19G>A (p.=)
c.-541G>A (p.=)
c.-702G>A (p.=)
n.81G>A
c.-515G>A (p.=)
n.512G>A
n.50G>A
n.57+19G>A
 ClinVar
17g.58692651G>CCA400336097RAD51Cc.8G>C (p.Gly3Ala)
n.79G>C
c.-241G>C (p.=)
c.-207+19G>C (p.=)
c.-541G>C (p.=)
c.-702G>C (p.=)
n.81G>C
c.-515G>C (p.=)
n.512G>C
n.50G>C
n.57+19G>C
 ClinVar
17g.58692651G>TCA400336104RAD51Cc.8G>T (p.Gly3Val)
n.79G>T
c.-241G>T (p.=)
c.-207+19G>T (p.=)
c.-541G>T (p.=)
c.-702G>T (p.=)
n.81G>T
c.-515G>T (p.=)
n.512G>T
n.50G>T
n.57+19G>T
17g.58692652G>ACA501074325RAD51Cc.9G>A (p.Gly3=)
n.80G>A
c.-240G>A (p.=)
c.-207+20G>A (p.=)
c.-540G>A (p.=)
c.-701G>A (p.=)
n.82G>A
c.-514G>A (p.=)
n.513G>A
n.51G>A
n.57+20G>A
17g.58692652G>CCA333900RAD51Cc.9G>C (p.Gly3=)
n.80G>C
c.-240G>C (p.=)
c.-207+20G>C (p.=)
c.-540G>C (p.=)
c.-701G>C (p.=)
n.82G>C
c.-514G>C (p.=)
n.513G>C
n.51G>C
n.57+20G>C
 ClinVar dbSNP ExAC gnomAD
17g.58692652G>TCA8677117RAD51Cc.9G>T (p.Gly3=)
n.80G>T
c.-240G>T (p.=)
c.-207+20G>T (p.=)
c.-540G>T (p.=)
c.-701G>T (p.=)
n.82G>T
c.-514G>T (p.=)
n.513G>T
n.51G>T
n.57+20G>T
 dbSNP ExAC gnomAD
17g.58692653A>CCA400336117RAD51Cc.10A>C (p.Lys4Gln)
n.81A>C
c.-239A>C (p.=)
c.-207+21A>C (p.=)
c.-539A>C (p.=)
c.-700A>C (p.=)
n.83A>C
c.-513A>C (p.=)
n.514A>C
n.52A>C
n.57+21A>C
17g.58692653A>GCA400336124RAD51Cc.10A>G (p.Lys4Glu)
n.81A>G
c.-239A>G (p.=)
c.-207+21A>G (p.=)
c.-539A>G (p.=)
c.-700A>G (p.=)
n.83A>G
c.-513A>G (p.=)
n.514A>G
n.52A>G
n.57+21A>G
17g.58692653A>TCA400336128RAD51Cc.10A>T (p.Lys4Ter)
n.81A>T
c.-239A>T (p.=)
c.-207+21A>T (p.=)
c.-539A>T (p.=)
c.-700A>T (p.=)
n.83A>T
c.-513A>T (p.=)
n.514A>T
n.52A>T
n.57+21A>T
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

Number of alleles fetched