Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.58692653del | CA913013104 | RAD51C | c.10del (p.Lys4ArgfsTer12) n.81del c.-239del (p.=) c.-207+21del (p.=) c.-539del (p.=) c.-700del (p.=) n.83del c.-513del (p.=) n.514del n.52del n.57+21del | |
17 | g.58692654A>C | CA400336133 | RAD51C | c.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 | |
17 | g.58692654A>G | CA400336138 | RAD51C | c.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 | |
17 | g.58692654A>T | CA400336141 | RAD51C | c.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 | |
17 | g.58692655G>A | CA8677118 | RAD51C | c.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 |
17 | g.58692655G>C | CA400336144 | RAD51C | c.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 | |
17 | g.58692655G>T | CA400336142 | RAD51C | c.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 | |
17 | g.58692656A>C | CA400336150 | RAD51C | c.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 |
17 | g.58692656A>G | CA400336151 | RAD51C | c.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 | |
17 | g.58692656A>T | CA400336152 | RAD51C | c.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 |
17 | g.58692657C>A | CA400336153 | RAD51C | c.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 | |
17 | g.58692657C>G | CA8677119 | RAD51C | c.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 |
17 | g.58692657C>T | CA288621 | RAD51C | c.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 |
17 | g.58692658G>A | CA501074326 | RAD51C | c.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 | |
17 | g.58692658G>C | CA8677120 | RAD51C | c.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 |
17 | g.58692658G>T | CA501074327 | RAD51C | c.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 |
17 | g.58692659T>A | CA400336197 | RAD51C | c.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 | |
17 | g.58692659T>C | CA8677121 | RAD51C | c.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 |
17 | g.58692659T>G | CA400336210 | RAD51C | c.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 |
17 | g.58692660T>A | CA8677122 | RAD51C | c.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 |
17 | g.58692660T>C | CA400336219 | RAD51C | c.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 | |
17 | g.58692660T>G | CA400336224 | RAD51C | c.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 | |
17 | g.58692661C>A | CA400336231 | RAD51C | c.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 |
17 | g.58692661C>G | CA400336227 | RAD51C | c.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 | |
17 | g.58692661C>T | CA8677123 | RAD51C | c.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 |
17 | g.58692662C>A | CA400336232 | RAD51C | c.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 |
17 | g.58692662C>G | CA8677124 | RAD51C | c.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 |
17 | g.58692662C>T | CA400336236 | RAD51C | c.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 |
17 | g.58692663G>A | CA292046832 | RAD51C | c.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 |
17 | g.58692663G>C | CA400336247 | RAD51C | c.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 |
17 | g.58692663G>T | CA400336251 | RAD51C | c.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 | |
17 | g.58692664C>A | CA501074329 | RAD51C | c.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 |
17 | g.58692664C>G | CA501074330 | RAD51C | c.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 | |
17 | g.58692664C>T | CA501074331 | RAD51C | c.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 |
17 | g.58692665T>A | CA400336256 | RAD51C | c.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 |
17 | g.58692665T>C | CA400336259 | RAD51C | c.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 | |
17 | g.58692665T>G | CA400336267 | RAD51C | c.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 | |
17 | g.58692666T>A | CA400336272 | RAD51C | c.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 | |
17 | g.58692666T>C | CA400336278 | RAD51C | c.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 | |
17 | g.58692666T>G | CA400336282 | RAD51C | c.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 | |
17 | g.58692667T>A | CA169336 | RAD51C | c.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 |
17 | g.58692667T>C | CA501074332 | RAD51C | c.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 | |
17 | g.58692667T>G | CA400336297 | RAD51C | c.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 | |
17 | g.58692668G>A | CA400336327 | RAD51C | c.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 | |
17 | g.58692668G>C | CA400336329 | RAD51C | c.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 |
17 | g.58692668G>T | CA400336331 | RAD51C | c.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 | |
17 | g.58692669A>C | CA400336335 | RAD51C | c.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 | |
17 | g.58692669A>G | CA400336344 | RAD51C | c.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 | |
17 | g.58692669A>T | CA400336345 | RAD51C | c.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 | |
17 | g.58692669del | CA915950639 | RAD51C | c.26del (p.Met10CysfsTer6) n.97del c.-223del (p.=) c.-207+37del (p.=) c.-523del (p.=) c.-684del (p.=) n.99del c.-497del (p.=) n.530del n.68del n.57+37del n.7del | ClinVar dbSNP |