| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32338197_32338391del | CA2580618074 | BRCA2 | c.3842_4036del (p.Lys1281_Asp1345del) c.3473_3667del (p.Lys1158_Asp1222del) n.3842_4036del | |
| 13 | g.32338274_32338296delinsGAAGAAATTACTGAAAATTACAA | CA2082822056 | BRCA2 | c.3919_3941delinsGAAGAAATTACTGAAAATTACAA (p.Glu1307=) c.3550_3572delinsGAAGAAATTACTGAAAATTACAA (p.Glu1184=) n.3919_3941delinsGAAGAAATTACTGAAAATTACAA | |
| 13 | g.32338275_32338296del | CA10589231 | BRCA2 | c.3920_3941del (p.Glu1307GlyfsTer21) c.3551_3572del (p.Glu1184GlyfsTer21) n.3920_3941del | ClinVar dbSNP |
| 13 | g.32338292_32338312del | CA2575387802 | BRCA2 | c.3937_3957del (p.Tyr1313_Asn1319del) c.3568_3588del (p.Tyr1190_Asn1196del) n.3937_3957del | |
| 13 | g.32338283A= | CA2082822155 | BRCA2 | c.3928A= (p.Thr1310=) c.3559A= (p.Thr1187=) n.3928A= | |
| 13 | g.32338283A>C | CA387778842 | BRCA2 | c.3928A>C (p.Thr1310Pro) c.3559A>C (p.Thr1187Pro) n.3928A>C | dbSNP |
| 13 | g.32338283A>G | CA387778843 | BRCA2 | c.3928A>G (p.Thr1310Ala) c.3559A>G (p.Thr1187Ala) n.3928A>G | ClinVar |
| 13 | g.32338283A>T | CA387778844 | BRCA2 | c.3928A>T (p.Thr1310Ser) c.3559A>T (p.Thr1187Ser) n.3928A>T | ClinVar dbSNP |
| 13 | g.32338283dup | CA916080547 | BRCA2 | c.3928dup (p.Thr1310AsnfsTer2) c.3559dup (p.Thr1187AsnfsTer2) n.3928dup | ClinVar dbSNP |
| 13 | g.32338283_32338284delinsAC | CA2082822157 | BRCA2 | c.3928_3929delinsAC (p.Thr1310=) c.3559_3560delinsAC (p.Thr1187=) n.3928_3929delinsAC | |
| 13 | g.32338284del | CA019210 | BRCA2 | c.3929del (p.Thr1310MetfsTer25) c.3560del (p.Thr1187MetfsTer25) n.3929del | ClinVar dbSNP |
| 13 | g.32338284C>A | CA387778845 | BRCA2 | c.3929C>A (p.Thr1310Asn) c.3560C>A (p.Thr1187Asn) n.3929C>A | dbSNP gnomAD v4 |
| 13 | g.32338284C= | CA2082822188 | BRCA2 | c.3929C= (p.Thr1310=) c.3560C= (p.Thr1187=) n.3929C= | |
| 13 | g.32338284C>G | CA387778846 | BRCA2 | c.3929C>G (p.Thr1310Ser) c.3560C>G (p.Thr1187Ser) n.3929C>G | dbSNP |
| 13 | g.32338284C>T | CA019205 | BRCA2 | c.3929C>T (p.Thr1310Ile) c.3560C>T (p.Thr1187Ile) n.3929C>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338285T>A | CA483437896 | BRCA2 | c.3930T>A (p.Thr1310=) c.3561T>A (p.Thr1187=) n.3930T>A | dbSNP |
| 13 | g.32338285T>C | CA019217 | BRCA2 | c.3930T>C (p.Thr1310=) c.3561T>C (p.Thr1187=) n.3930T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338285T>G | CA483437898 | BRCA2 | c.3930T>G (p.Thr1310=) c.3561T>G (p.Thr1187=) n.3930T>G | |
| 13 | g.32338285T= | CA2082822200 | BRCA2 | c.3930T= (p.Thr1310=) c.3561T= (p.Thr1187=) n.3930T= | |
| 13 | g.32338285_32338296delinsTGAAAATTACAA | CA2082822209 | BRCA2 | c.3930_3941delinsTGAAAATTACAA (p.Thr1310=) c.3561_3572delinsTGAAAATTACAA (p.Thr1187=) n.3930_3941delinsTGAAAATTACAA | |
| 13 | g.32338286G>A | CA387778847 | BRCA2 | c.3931G>A (p.Glu1311Lys) c.3562G>A (p.Glu1188Lys) n.3931G>A | dbSNP gnomAD v4 |
| 13 | g.32338286G>C | CA387778849 | BRCA2 | c.3931G>C (p.Glu1311Gln) c.3562G>C (p.Glu1188Gln) n.3931G>C | dbSNP |
| 13 | g.32338286G= | CA2082822234 | BRCA2 | c.3931G= (p.Glu1311=) c.3562G= (p.Glu1188=) n.3931G= | |
| 13 | g.32338286G>T | CA387778848 | BRCA2 | c.3931G>T (p.Glu1311Ter) c.3562G>T (p.Glu1188Ter) n.3931G>T | |
| 13 | g.32338288_32338298del | CA658798134 | BRCA2 | c.3933_3943del (p.Asn1312LysfsTer3) c.3564_3574del (p.Asn1189LysfsTer3) n.3933_3943del | ClinVar dbSNP |
| 13 | g.32338287A= | CA2082822241 | BRCA2 | c.3932A= (p.Glu1311=) c.3563A= (p.Glu1188=) n.3932A= | |
| 13 | g.32338287A>C | CA387778850 | BRCA2 | c.3932A>C (p.Glu1311Ala) c.3563A>C (p.Glu1188Ala) n.3932A>C | ClinVar dbSNP |
| 13 | g.32338287A>G | CA387778852 | BRCA2 | c.3932A>G (p.Glu1311Gly) c.3563A>G (p.Glu1188Gly) n.3932A>G | ClinVar dbSNP |
| 13 | g.32338287A>T | CA387778851 | BRCA2 | c.3932A>T (p.Glu1311Val) c.3563A>T (p.Glu1188Val) n.3932A>T | dbSNP |
| 13 | g.32338290dup | CA913190943 | BRCA2 | c.3935dup (p.Asn1312LysfsTer7) c.3566dup (p.Asn1189LysfsTer7) n.3935dup | ClinVar dbSNP |
| 13 | g.32338290del | CA2580087230 | BRCA2 | c.3935del (p.Asn1312IlefsTer23) c.3566del (p.Asn1189IlefsTer23) n.3935del | ClinVar |
| 13 | g.32338289_32338290del | CA2580614670 | BRCA2 | c.3934_3935del (p.Asn1312LeufsTer6) c.3565_3566del (p.Asn1189LeufsTer6) n.3934_3935del | ClinVar |
| 13 | g.32338288A>C | CA387778853 | BRCA2 | c.3933A>C (p.Glu1311Asp) c.3564A>C (p.Glu1188Asp) n.3933A>C | |
| 13 | g.32338288A>G | CA483437903 | BRCA2 | c.3933A>G (p.Glu1311=) c.3564A>G (p.Glu1188=) n.3933A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338288A>T | CA387778854 | BRCA2 | c.3933A>T (p.Glu1311Asp) c.3564A>T (p.Glu1188Asp) n.3933A>T | |
| 13 | g.32338288_32338307delinsAAATTACAAGAGAAATACTG | CA2082822250 | BRCA2 | c.3933_3952delinsAAATTACAAGAGAAATACTG (p.Glu1311=) c.3564_3583delinsAAATTACAAGAGAAATACTG (p.Glu1188=) n.3933_3952delinsAAATTACAAGAGAAATACTG | |
| 13 | g.32338289A>C | CA387778855 | BRCA2 | c.3934A>C (p.Asn1312His) c.3565A>C (p.Asn1189His) n.3934A>C | |
| 13 | g.32338289A>G | CA387778856 | BRCA2 | c.3934A>G (p.Asn1312Asp) c.3565A>G (p.Asn1189Asp) n.3934A>G | gnomAD v4 |
| 13 | g.32338289A>T | CA387778857 | BRCA2 | c.3934A>T (p.Asn1312Tyr) c.3565A>T (p.Asn1189Tyr) n.3934A>T | dbSNP |
| 13 | g.32338291_32338309del | CA019222 | BRCA2 | c.3936_3954del (p.Asn1312LysfsTer17) c.3567_3585del (p.Asn1189LysfsTer17) n.3936_3954del | ClinVar dbSNP |
| 13 | g.32338290A>C | CA387778858 | BRCA2 | c.3935A>C (p.Asn1312Thr) c.3566A>C (p.Asn1189Thr) n.3935A>C | |
| 13 | g.32338290A>G | CA387778859 | BRCA2 | c.3935A>G (p.Asn1312Ser) c.3566A>G (p.Asn1189Ser) n.3935A>G | |
| 13 | g.32338290A>T | CA387778860 | BRCA2 | c.3935A>T (p.Asn1312Ile) c.3566A>T (p.Asn1189Ile) n.3935A>T | |
| 13 | g.32338290_32338291delinsAT | CA2082822257 | BRCA2 | c.3935_3936delinsAT (p.Asn1312=) c.3566_3567delinsAT (p.Asn1189=) n.3935_3936delinsAT | |
| 13 | g.32338291T>A | CA387778861 | BRCA2 | c.3936T>A (p.Asn1312Lys) c.3567T>A (p.Asn1189Lys) n.3936T>A | dbSNP |
| 13 | g.32338291T>C | CA10579596 | BRCA2 | c.3936T>C (p.Asn1312=) c.3567T>C (p.Asn1189=) n.3936T>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338291T>G | CA387778862 | BRCA2 | c.3936T>G (p.Asn1312Lys) c.3567T>G (p.Asn1189Lys) n.3936T>G | ClinVar dbSNP |
| 13 | g.32338291T= | CA2082822271 | BRCA2 | c.3936T= (p.Asn1312=) c.3567T= (p.Asn1189=) n.3936T= | |
| 13 | g.32338292del | CA913190944 | BRCA2 | c.3937del (p.Tyr1313ThrfsTer22) c.3568del (p.Tyr1190ThrfsTer22) n.3937del | ClinVar dbSNP |
| 13 | g.32338292T>A | CA387778863 | BRCA2 | c.3937T>A (p.Tyr1313Asn) c.3568T>A (p.Tyr1190Asn) n.3937T>A | dbSNP |
| 13 | g.32338292T>C | CA387778865 | BRCA2 | c.3937T>C (p.Tyr1313His) c.3568T>C (p.Tyr1190His) n.3937T>C | |
| 13 | g.32338292T>G | CA387778864 | BRCA2 | c.3937T>G (p.Tyr1313Asp) c.3568T>G (p.Tyr1190Asp) n.3937T>G | ClinVar |
| 13 | g.32338293A= | CA2082822283 | BRCA2 | c.3938A= (p.Tyr1313=) c.3569A= (p.Tyr1190=) n.3938A= | |
| 13 | g.32338293A>C | CA019228 | BRCA2 | c.3938A>C (p.Tyr1313Ser) c.3569A>C (p.Tyr1190Ser) n.3938A>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338293A>G | CA019236 | BRCA2 | c.3938A>G (p.Tyr1313Cys) c.3569A>G (p.Tyr1190Cys) n.3938A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338293A>T | CA387778866 | BRCA2 | c.3938A>T (p.Tyr1313Phe) c.3569A>T (p.Tyr1190Phe) n.3938A>T | dbSNP |
| 13 | g.32338293dup | CA2573149353 | BRCA2 | c.3938dup (p.Tyr1313Ter) c.3569dup (p.Tyr1190Ter) n.3938dup | ClinVar dbSNP |
| 13 | g.32338293_32338294delinsAC | CA2082822284 | BRCA2 | c.3938_3939delinsAC (p.Tyr1313=) c.3569_3570delinsAC (p.Tyr1190=) n.3938_3939delinsAC | |
| 13 | g.32338294_32338298del | CA2573053808 | BRCA2 | c.3939_3943del (p.Tyr1313Ter) c.3570_3574del (p.Tyr1190Ter) n.3939_3943del | ClinVar dbSNP |
| 13 | g.32338294del | CA019249 | BRCA2 | c.3939del (p.Tyr1313Ter) c.3570del (p.Tyr1190Ter) n.3939del | ClinVar dbSNP |
| 13 | g.32338294C>A | CA019241 | BRCA2 | c.3939C>A (p.Tyr1313Ter) c.3570C>A (p.Tyr1190Ter) n.3939C>A | ClinVar dbSNP |
| 13 | g.32338294C= | CA2082822300 | BRCA2 | c.3939C= (p.Tyr1313=) c.3570C= (p.Tyr1190=) n.3939C= | |
| 13 | g.32338294C>G | CA019246 | BRCA2 | c.3939C>G (p.Tyr1313Ter) c.3570C>G (p.Tyr1190Ter) n.3939C>G | ClinVar dbSNP |
| 13 | g.32338294C>T | CA483437911 | BRCA2 | c.3939C>T (p.Tyr1313=) c.3570C>T (p.Tyr1190=) n.3939C>T | dbSNP gnomAD v4 |
| 13 | g.32338294_32338296delinsCAA | CA2082822307 | BRCA2 | c.3939_3941delinsCAA (p.Tyr1313=) c.3570_3572delinsCAA (p.Tyr1190=) n.3939_3941delinsCAA | |
| 13 | g.32338295A>C | CA387778867 | BRCA2 | c.3940A>C (p.Lys1314Gln) c.3571A>C (p.Lys1191Gln) n.3940A>C | gnomAD v4 |
| 13 | g.32338295A>G | CA387778868 | BRCA2 | c.3940A>G (p.Lys1314Glu) c.3571A>G (p.Lys1191Glu) n.3940A>G | dbSNP |
| 13 | g.32338295A>T | CA387778869 | BRCA2 | c.3940A>T (p.Lys1314Ter) c.3571A>T (p.Lys1191Ter) n.3940A>T | ClinVar |
| 13 | g.32338295_32338296del | CA658683802 | BRCA2 | c.3940_3941del (p.Lys1314GlufsTer4) c.3571_3572del (p.Lys1191GlufsTer4) n.3940_3941del | ClinVar dbSNP |
| 13 | g.32338296A= | CA2082822326 | BRCA2 | c.3941A= (p.Lys1314=) c.3572A= (p.Lys1191=) n.3941A= | |
| 13 | g.32338296A>C | CA387778871 | BRCA2 | c.3941A>C (p.Lys1314Thr) c.3572A>C (p.Lys1191Thr) n.3941A>C | |
| 13 | g.32338296A>G | CA387778872 | BRCA2 | c.3941A>G (p.Lys1314Arg) c.3572A>G (p.Lys1191Arg) n.3941A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338296A>T | CA387778870 | BRCA2 | c.3941A>T (p.Lys1314Met) c.3572A>T (p.Lys1191Met) n.3941A>T | dbSNP |
| 13 | g.32338297G>A | CA16607463 | BRCA2 | c.3942G>A (p.Lys1314=) c.3573G>A (p.Lys1191=) n.3942G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338297G>C | CA247506205 | BRCA2 | c.3942G>C (p.Lys1314Asn) c.3573G>C (p.Lys1191Asn) n.3942G>C | dbSNP |
| 13 | g.32338297G= | CA2082822342 | BRCA2 | c.3942G= (p.Lys1314=) c.3573G= (p.Lys1191=) n.3942G= | |
| 13 | g.32338297G>T | CA387778873 | BRCA2 | c.3942G>T (p.Lys1314Asn) c.3573G>T (p.Lys1191Asn) n.3942G>T | gnomAD v4 |
| 13 | g.32338298A>C | CA483437919 | BRCA2 | c.3943A>C (p.Arg1315=) c.3574A>C (p.Arg1192=) n.3943A>C | |
| 13 | g.32338298A>G | CA387778874 | BRCA2 | c.3943A>G (p.Arg1315Gly) c.3574A>G (p.Arg1192Gly) n.3943A>G | |
| 13 | g.32338298A>T | CA387778875 | BRCA2 | c.3943A>T (p.Arg1315Ter) c.3574A>T (p.Arg1192Ter) n.3943A>T | |
| 13 | g.32338299G>A | CA019254 | BRCA2 | c.3944G>A (p.Arg1315Lys) c.3575G>A (p.Arg1192Lys) n.3944G>A | ClinVar dbSNP |
| 13 | g.32338299G>C | CA387778876 | BRCA2 | c.3944G>C (p.Arg1315Thr) c.3575G>C (p.Arg1192Thr) n.3944G>C | ClinVar dbSNP |
| 13 | g.32338299G= | CA2082822345 | BRCA2 | c.3944G= (p.Arg1315=) c.3575G= (p.Arg1192=) n.3944G= | |
| 13 | g.32338299G>T | CA387778877 | BRCA2 | c.3944G>T (p.Arg1315Ile) c.3575G>T (p.Arg1192Ile) n.3944G>T | gnomAD v4 |
| 13 | g.32338300A>C | CA387778878 | BRCA2 | c.3945A>C (p.Arg1315Ser) c.3576A>C (p.Arg1192Ser) n.3945A>C | |
| 13 | g.32338300A>G | CA483437921 | BRCA2 | c.3945A>G (p.Arg1315=) c.3576A>G (p.Arg1192=) n.3945A>G | gnomAD v4 |
| 13 | g.32338300A>T | CA387778879 | BRCA2 | c.3945A>T (p.Arg1315Ser) c.3576A>T (p.Arg1192Ser) n.3945A>T | ClinVar dbSNP |
| 13 | g.32338301_32338302del | CA2580087231 | BRCA2 | c.3946_3947del (p.Asn1316TyrfsTer2) c.3577_3578del (p.Asn1193TyrfsTer2) n.3946_3947del | ClinVar |
| 13 | g.32338301A>C | CA387778880 | BRCA2 | c.3946A>C (p.Asn1316His) c.3577A>C (p.Asn1193His) n.3946A>C | |
| 13 | g.32338301A>G | CA387778881 | BRCA2 | c.3946A>G (p.Asn1316Asp) c.3577A>G (p.Asn1193Asp) n.3946A>G | gnomAD v4 |
| 13 | g.32338301A>T | CA387778882 | BRCA2 | c.3946A>T (p.Asn1316Tyr) c.3577A>T (p.Asn1193Tyr) n.3946A>T | |
| 13 | g.32338302A= | CA2082822351 | BRCA2 | c.3947A= (p.Asn1316=) c.3578A= (p.Asn1193=) n.3947A= | |
| 13 | g.32338302A>C | CA387778885 | BRCA2 | c.3947A>C (p.Asn1316Thr) c.3578A>C (p.Asn1193Thr) n.3947A>C | |
| 13 | g.32338302A>G | CA387778883 | BRCA2 | c.3947A>G (p.Asn1316Ser) c.3578A>G (p.Asn1193Ser) n.3947A>G | ClinVar dbSNP |
| 13 | g.32338302A>T | CA387778884 | BRCA2 | c.3947A>T (p.Asn1316Ile) c.3578A>T (p.Asn1193Ile) n.3947A>T | dbSNP |
| 13 | g.32338303T>A | CA387778886 | BRCA2 | c.3948T>A (p.Asn1316Lys) c.3579T>A (p.Asn1193Lys) n.3948T>A | dbSNP |
| 13 | g.32338303T>C | CA483437928 | BRCA2 | c.3948T>C (p.Asn1316=) c.3579T>C (p.Asn1193=) n.3948T>C | ClinVar |
| 13 | g.32338303T>G | CA387778887 | BRCA2 | c.3948T>G (p.Asn1316Lys) c.3579T>G (p.Asn1193Lys) n.3948T>G | dbSNP |
| 13 | g.32338304A= | CA2082822360 | BRCA2 | c.3949A= (p.Thr1317=) c.3580A= (p.Thr1194=) n.3949A= | |
| 13 | g.32338304A>C | CA387778888 | BRCA2 | c.3949A>C (p.Thr1317Pro) c.3580A>C (p.Thr1194Pro) n.3949A>C | dbSNP |
| 13 | g.32338304A>G | CA387778889 | BRCA2 | c.3949A>G (p.Thr1317Ala) c.3580A>G (p.Thr1194Ala) n.3949A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338304A>T | CA019259 | BRCA2 | c.3949A>T (p.Thr1317Ser) c.3580A>T (p.Thr1194Ser) n.3949A>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338305del | CA2499222148 | BRCA2 | c.3950del (p.Thr1317MetfsTer18) c.3581del (p.Thr1194MetfsTer18) n.3950del | |
| 13 | g.32338305C>A | CA387778890 | BRCA2 | c.3950C>A (p.Thr1317Asn) c.3581C>A (p.Thr1194Asn) n.3950C>A | dbSNP gnomAD v4 |
| 13 | g.32338305C= | CA2082822380 | BRCA2 | c.3950C= (p.Thr1317=) c.3581C= (p.Thr1194=) n.3950C= | |
| 13 | g.32338305C>G | CA387778891 | BRCA2 | c.3950C>G (p.Thr1317Ser) c.3581C>G (p.Thr1194Ser) n.3950C>G | ClinVar dbSNP |
| 13 | g.32338305C>T | CA387778892 | BRCA2 | c.3950C>T (p.Thr1317Ile) c.3581C>T (p.Thr1194Ile) n.3950C>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338306T>A | CA483437931 | BRCA2 | c.3951T>A (p.Thr1317=) c.3582T>A (p.Thr1194=) n.3951T>A | |
| 13 | g.32338306T>C | CA6940734 | BRCA2 | c.3951T>C (p.Thr1317=) c.3582T>C (p.Thr1194=) n.3951T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338306T>G | CA483437932 | BRCA2 | c.3951T>G (p.Thr1317=) c.3582T>G (p.Thr1194=) n.3951T>G | |
| 13 | g.32338306T= | CA2082822388 | BRCA2 | c.3951T= (p.Thr1317=) c.3582T= (p.Thr1194=) n.3951T= | |
| 13 | g.32338307G>A | CA387778893 | BRCA2 | c.3952G>A (p.Glu1318Lys) c.3583G>A (p.Glu1195Lys) n.3952G>A | ClinVar gnomAD v4 |
| 13 | g.32338307G>C | CA387778894 | BRCA2 | c.3952G>C (p.Glu1318Gln) c.3583G>C (p.Glu1195Gln) n.3952G>C | dbSNP |
| 13 | g.32338307G>T | CA387778895 | BRCA2 | c.3952G>T (p.Glu1318Ter) c.3583G>T (p.Glu1195Ter) n.3952G>T | |
| 13 | g.32338308A>C | CA387778898 | BRCA2 | c.3953A>C (p.Glu1318Ala) c.3584A>C (p.Glu1195Ala) n.3953A>C | |
| 13 | g.32338308A>G | CA387778897 | BRCA2 | c.3953A>G (p.Glu1318Gly) c.3584A>G (p.Glu1195Gly) n.3953A>G | gnomAD v4 |
| 13 | g.32338308A>T | CA387778896 | BRCA2 | c.3953A>T (p.Glu1318Val) c.3584A>T (p.Glu1195Val) n.3953A>T | dbSNP |
| 13 | g.32338311del | CA2580087232 | BRCA2 | c.3956del (p.Asn1319MetfsTer16) c.3587del (p.Asn1196MetfsTer16) n.3956del | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338309A>C | CA387778899 | BRCA2 | c.3954A>C (p.Glu1318Asp) c.3585A>C (p.Glu1195Asp) n.3954A>C | |
| 13 | g.32338309A>G | CA483437939 | BRCA2 | c.3954A>G (p.Glu1318=) c.3585A>G (p.Glu1195=) n.3954A>G | dbSNP |
| 13 | g.32338309A>T | CA387778900 | BRCA2 | c.3954A>T (p.Glu1318Asp) c.3585A>T (p.Glu1195Asp) n.3954A>T | dbSNP |
| 13 | g.32338309_32338313delinsAAATG | CA2082822395 | BRCA2 | c.3954_3958delinsAAATG (p.Glu1318=) c.3585_3589delinsAAATG (p.Glu1195=) n.3954_3958delinsAAATG | |
| 13 | g.32338310A>C | CA387778901 | BRCA2 | c.3955A>C (p.Asn1319His) c.3586A>C (p.Asn1196His) n.3955A>C | |
| 13 | g.32338310A>G | CA387778902 | BRCA2 | c.3955A>G (p.Asn1319Asp) c.3586A>G (p.Asn1196Asp) n.3955A>G | dbSNP |
| 13 | g.32338310A>T | CA387778903 | BRCA2 | c.3955A>T (p.Asn1319Tyr) c.3586A>T (p.Asn1196Tyr) n.3955A>T | dbSNP |
| 13 | g.32338312_32338315del | CA019261 | BRCA2 | c.3957_3960del (p.Asn1319LysfsTer15) c.3588_3591del (p.Asn1196LysfsTer15) n.3957_3960del | ClinVar dbSNP |
| 13 | g.32338311A>C | CA387778904 | BRCA2 | c.3956A>C (p.Asn1319Thr) c.3587A>C (p.Asn1196Thr) n.3956A>C | |
| 13 | g.32338311A>G | CA387778905 | BRCA2 | c.3956A>G (p.Asn1319Ser) c.3587A>G (p.Asn1196Ser) n.3956A>G | dbSNP |
| 13 | g.32338311A>T | CA387778906 | BRCA2 | c.3956A>T (p.Asn1319Ile) c.3587A>T (p.Asn1196Ile) n.3956A>T | |
| 13 | g.32338311_32338313delinsATG | CA2082822406 | BRCA2 | c.3956_3958delinsATG (p.Asn1319=) c.3587_3589delinsATG (p.Asn1196=) n.3956_3958delinsATG | |
| 13 | g.32338313_32338318del | CA2580087233 | BRCA2 | c.3958_3963del (p.Glu1320_Asp1321del) c.3589_3594del (p.Glu1197_Asp1198del) n.3958_3963del | ClinVar dbSNP |
| 13 | g.32338312T>A | CA387778907 | BRCA2 | c.3957T>A (p.Asn1319Lys) c.3588T>A (p.Asn1196Lys) n.3957T>A | dbSNP |
| 13 | g.32338312T>C | CA483437945 | BRCA2 | c.3957T>C (p.Asn1319=) c.3588T>C (p.Asn1196=) n.3957T>C | ClinVar dbSNP |
| 13 | g.32338312T>G | CA387778908 | BRCA2 | c.3957T>G (p.Asn1319Lys) c.3588T>G (p.Asn1196Lys) n.3957T>G | dbSNP |
| 13 | g.32338312T= | CA2082822421 | BRCA2 | c.3957T= (p.Asn1319=) c.3588T= (p.Asn1196=) n.3957T= | |
| 13 | g.32338312_32338313del | CA10589232 | BRCA2 | c.3957_3958del (p.Asn1319LysfsTer3) c.3588_3589del (p.Asn1196LysfsTer3) n.3957_3958del | ClinVar dbSNP |
| 13 | g.32338313G>A | CA10583097 | BRCA2 | c.3958G>A (p.Glu1320Lys) c.3589G>A (p.Glu1197Lys) n.3958G>A | ClinVar dbSNP |
| 13 | g.32338313G>C | CA387778909 | BRCA2 | c.3958G>C (p.Glu1320Gln) c.3589G>C (p.Glu1197Gln) n.3958G>C | dbSNP |
| 13 | g.32338313G= | CA2082822445 | BRCA2 | c.3958G= (p.Glu1320=) c.3589G= (p.Glu1197=) n.3958G= | |
| 13 | g.32338313G>T | CA019267 | BRCA2 | c.3958G>T (p.Glu1320Ter) c.3589G>T (p.Glu1197Ter) n.3958G>T | ClinVar dbSNP |
| 13 | g.32338314A>C | CA387778910 | BRCA2 | c.3959A>C (p.Glu1320Ala) c.3590A>C (p.Glu1197Ala) n.3959A>C | ClinVar |
| 13 | g.32338314A>G | CA387778912 | BRCA2 | c.3959A>G (p.Glu1320Gly) c.3590A>G (p.Glu1197Gly) n.3959A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338314A>T | CA387778911 | BRCA2 | c.3959A>T (p.Glu1320Val) c.3590A>T (p.Glu1197Val) n.3959A>T | dbSNP |
| 13 | g.32338315A= | CA2082822458 | BRCA2 | c.3960A= (p.Glu1320=) c.3591A= (p.Glu1197=) n.3960A= | |
| 13 | g.32338315A>C | CA387778913 | BRCA2 | c.3960A>C (p.Glu1320Asp) c.3591A>C (p.Glu1197Asp) n.3960A>C | ClinVar |
| 13 | g.32338315A>G | CA483437949 | BRCA2 | c.3960A>G (p.Glu1320=) c.3591A>G (p.Glu1197=) n.3960A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338315A>T | CA387778914 | BRCA2 | c.3960A>T (p.Glu1320Asp) c.3591A>T (p.Glu1197Asp) n.3960A>T | dbSNP gnomAD v4 |
| 13 | g.32338316_32338326del | CA2697551724 | BRCA2 | c.3961_3971del (p.Asp1321TyrfsTer5) c.3592_3602del (p.Asp1198TyrfsTer5) n.3961_3971del | ClinVar |
| 13 | g.32338316G>A | CA6940736 | BRCA2 | c.3961G>A (p.Asp1321Asn) c.3592G>A (p.Asp1198Asn) n.3961G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338316G>C | CA6940735 | BRCA2 | c.3961G>C (p.Asp1321His) c.3592G>C (p.Asp1198His) n.3961G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338316G= | CA2082822467 | BRCA2 | c.3961G= (p.Asp1321=) c.3592G= (p.Asp1198=) n.3961G= | |
| 13 | g.32338316G>T | CA387778915 | BRCA2 | c.3961G>T (p.Asp1321Tyr) c.3592G>T (p.Asp1198Tyr) n.3961G>T | dbSNP |
| 13 | g.32338317A= | CA2082822469 | BRCA2 | c.3962A= (p.Asp1321=) c.3593A= (p.Asp1198=) n.3962A= | |
| 13 | g.32338317A>C | CA387778916 | BRCA2 | c.3962A>C (p.Asp1321Ala) c.3593A>C (p.Asp1198Ala) n.3962A>C | |
| 13 | g.32338317A>G | CA019277 | BRCA2 | c.3962A>G (p.Asp1321Gly) c.3593A>G (p.Asp1198Gly) n.3962A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338317A>T | CA247506226 | BRCA2 | c.3962A>T (p.Asp1321Val) c.3593A>T (p.Asp1198Val) n.3962A>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338318T>A | CA387778917 | BRCA2 | c.3963T>A (p.Asp1321Glu) c.3594T>A (p.Asp1198Glu) n.3963T>A | dbSNP |
| 13 | g.32338318T>C | CA483437956 | BRCA2 | c.3963T>C (p.Asp1321=) c.3594T>C (p.Asp1198=) n.3963T>C | ClinVar dbSNP |
| 13 | g.32338318T>G | CA387778918 | BRCA2 | c.3963T>G (p.Asp1321Glu) c.3594T>G (p.Asp1198Glu) n.3963T>G | dbSNP |
| 13 | g.32338318_32338321delinsTAAC | CA2082822473 | BRCA2 | c.3963_3966delinsTAAC (p.Asp1321=) c.3594_3597delinsTAAC (p.Asp1198=) n.3963_3966delinsTAAC | |
| 13 | g.32338319A= | CA2082822483 | BRCA2 | c.3964A= (p.Asn1322=) c.3595A= (p.Asn1199=) n.3964A= | |
| 13 | g.32338319A>C | CA387778920 | BRCA2 | c.3964A>C (p.Asn1322His) c.3595A>C (p.Asn1199His) n.3964A>C | ClinVar dbSNP |
| 13 | g.32338319A>G | CA10586065 | BRCA2 | c.3964A>G (p.Asn1322Asp) c.3595A>G (p.Asn1199Asp) n.3964A>G | ClinVar dbSNP |
| 13 | g.32338319A>T | CA387778919 | BRCA2 | c.3964A>T (p.Asn1322Tyr) c.3595A>T (p.Asn1199Tyr) n.3964A>T | dbSNP |
| 13 | g.32338321_32338323del | CA019288 | BRCA2 | c.3966_3968del (p.Asn1322del) c.3597_3599del (p.Asn1199del) n.3966_3968del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338320A= | CA2082822500 | BRCA2 | c.3965A= (p.Asn1322=) c.3596A= (p.Asn1199=) n.3965A= | |
| 13 | g.32338320A>C | CA019283 | BRCA2 | c.3965A>C (p.Asn1322Thr) c.3596A>C (p.Asn1199Thr) n.3965A>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338320A>G | CA387778921 | BRCA2 | c.3965A>G (p.Asn1322Ser) c.3596A>G (p.Asn1199Ser) n.3965A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338320A>T | CA387778922 | BRCA2 | c.3965A>T (p.Asn1322Ile) c.3596A>T (p.Asn1199Ile) n.3965A>T | dbSNP |
| 13 | g.32338321C>A | CA387778923 | BRCA2 | c.3966C>A (p.Asn1322Lys) c.3597C>A (p.Asn1199Lys) n.3966C>A | dbSNP gnomAD v4 |
| 13 | g.32338321C= | CA2082822520 | BRCA2 | c.3966C= (p.Asn1322=) c.3597C= (p.Asn1199=) n.3966C= | |
| 13 | g.32338321C>G | CA019298 | BRCA2 | c.3966C>G (p.Asn1322Lys) c.3597C>G (p.Asn1199Lys) n.3966C>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338321C>T | CA019300 | BRCA2 | c.3966C>T (p.Asn1322=) c.3597C>T (p.Asn1199=) n.3966C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338321_32338325delinsCAAAT | CA2082822513 | BRCA2 | c.3966_3970delinsCAAAT (p.Asn1322=) c.3597_3601delinsCAAAT (p.Asn1199=) n.3966_3970delinsCAAAT | |
| 13 | g.32338322A= | CA2082822530 | BRCA2 | c.3967A= (p.Lys1323=) c.3598A= (p.Lys1200=) n.3967A= | |
| 13 | g.32338322A>C | CA387778924 | BRCA2 | c.3967A>C (p.Lys1323Gln) c.3598A>C (p.Lys1200Gln) n.3967A>C | ClinVar |
| 13 | g.32338322A>G | CA387778925 | BRCA2 | c.3967A>G (p.Lys1323Glu) c.3598A>G (p.Lys1200Glu) n.3967A>G | ClinVar dbSNP |
| 13 | g.32338322A>T | CA019306 | BRCA2 | c.3967A>T (p.Lys1323Ter) c.3598A>T (p.Lys1200Ter) n.3967A>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338323_32338324del | CA2499222149 | BRCA2 | c.3968_3969del (p.Lys1323IlefsTer6) c.3599_3600del (p.Lys1200IlefsTer6) n.3968_3969del | ClinVar dbSNP |
| 13 | g.32338323_32338326del | CA10589233 | BRCA2 | c.3968_3971del (p.Lys1323IlefsTer11) c.3599_3602del (p.Lys1200IlefsTer11) n.3968_3971del | ClinVar dbSNP |
| 13 | g.32338323A= | CA2082822542 | BRCA2 | c.3968A= (p.Lys1323=) c.3599A= (p.Lys1200=) n.3968A= | |
| 13 | g.32338323A>C | CA387778928 | BRCA2 | c.3968A>C (p.Lys1323Thr) c.3599A>C (p.Lys1200Thr) n.3968A>C | |
| 13 | g.32338323A>G | CA387778927 | BRCA2 | c.3968A>G (p.Lys1323Arg) c.3599A>G (p.Lys1200Arg) n.3968A>G | ClinVar dbSNP |
| 13 | g.32338323A>T | CA387778926 | BRCA2 | c.3968A>T (p.Lys1323Ile) c.3599A>T (p.Lys1200Ile) n.3968A>T | dbSNP |
| 13 | g.32338323_32338325delinsAAT | CA2082822541 | BRCA2 | c.3968_3970delinsAAT (p.Lys1323=) c.3599_3601delinsAAT (p.Lys1200=) n.3968_3970delinsAAT | |
| 13 | g.32338324A= | CA2082822557 | BRCA2 | c.3969A= (p.Lys1323=) c.3600A= (p.Lys1200=) n.3969A= | |
| 13 | g.32338324A>C | CA387778929 | BRCA2 | c.3969A>C (p.Lys1323Asn) c.3600A>C (p.Lys1200Asn) n.3969A>C | |
| 13 | g.32338324A>G | CA483437968 | BRCA2 | c.3969A>G (p.Lys1323=) c.3600A>G (p.Lys1200=) n.3969A>G | ClinVar dbSNP |
| 13 | g.32338324A>T | CA387778930 | BRCA2 | c.3969A>T (p.Lys1323Asn) c.3600A>T (p.Lys1200Asn) n.3969A>T | |
| 13 | g.32338327_32338328del | CA10589234 | BRCA2 | c.3972_3973del (p.Thr1325CysfsTer4) c.3603_3604del (p.Thr1202CysfsTer4) n.3972_3973del | ClinVar dbSNP |
| 13 | g.32338324_32338325insCT | CA913188551 | BRCA2 | c.3969_3970insCT (p.Tyr1324LeufsTer12) c.3600_3601insCT (p.Tyr1201LeufsTer12) n.3969_3970insCT | ClinVar |
| 13 | g.32338325T>A | CA387778931 | BRCA2 | c.3970T>A (p.Tyr1324Asn) c.3601T>A (p.Tyr1201Asn) n.3970T>A | dbSNP |
| 13 | g.32338325T>C | CA10584444 | BRCA2 | c.3970T>C (p.Tyr1324His) c.3601T>C (p.Tyr1201His) n.3970T>C | ClinVar dbSNP |
| 13 | g.32338325T>G | CA387778932 | BRCA2 | c.3970T>G (p.Tyr1324Asp) c.3601T>G (p.Tyr1201Asp) n.3970T>G | dbSNP |
| 13 | g.32338325T= | CA2082822565 | BRCA2 | c.3970T= (p.Tyr1324=) c.3601T= (p.Tyr1201=) n.3970T= | |
| 13 | g.32338325_32338326delinsTA | CA2082822562 | BRCA2 | c.3970_3971delinsTA (p.Tyr1324=) c.3601_3602delinsTA (p.Tyr1201=) n.3970_3971delinsTA | |
| 13 | g.32338326del | CA658761227 | BRCA2 | c.3971del (p.Tyr1324LeufsTer11) c.3602del (p.Tyr1201LeufsTer11) n.3971del | ClinVar dbSNP |
| 13 | g.32338326A= | CA2082822588 | BRCA2 | c.3971A= (p.Tyr1324=) c.3602A= (p.Tyr1201=) n.3971A= | |
| 13 | g.32338326A>C | CA387778933 | BRCA2 | c.3971A>C (p.Tyr1324Ser) c.3602A>C (p.Tyr1201Ser) n.3971A>C | ClinVar dbSNP |
| 13 | g.32338326A>G | CA387778934 | BRCA2 | c.3971A>G (p.Tyr1324Cys) c.3602A>G (p.Tyr1201Cys) n.3971A>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338326A>T | CA387778935 | BRCA2 | c.3971A>T (p.Tyr1324Phe) c.3602A>T (p.Tyr1201Phe) n.3971A>T | |
| 13 | g.32338326_32338330delinsATACT | CA2082822578 | BRCA2 | c.3971_3975delinsATACT (p.Tyr1324=) c.3602_3606delinsATACT (p.Tyr1201=) n.3971_3975delinsATACT | |
| 13 | g.32338327T>A | CA387778936 | BRCA2 | c.3972T>A (p.Tyr1324Ter) c.3603T>A (p.Tyr1201Ter) n.3972T>A | dbSNP gnomAD v4 |
| 13 | g.32338327T>C | CA483437973 | BRCA2 | c.3972T>C (p.Tyr1324=) c.3603T>C (p.Tyr1201=) n.3972T>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338327T>G | CA387778937 | BRCA2 | c.3972T>G (p.Tyr1324Ter) c.3603T>G (p.Tyr1201Ter) n.3972T>G | ClinVar dbSNP |
| 13 | g.32338327T= | CA2082822600 | BRCA2 | c.3972T= (p.Tyr1324=) c.3603T= (p.Tyr1201=) n.3972T= | |
| 13 | g.32338327_32338330del | CA10589235 | BRCA2 | c.3972_3975del (p.Tyr1324Ter) c.3603_3606del (p.Tyr1201Ter) n.3972_3975del | ClinVar dbSNP |
| 13 | g.32338328A>C | CA387778939 | BRCA2 | c.3973A>C (p.Thr1325Pro) c.3604A>C (p.Thr1202Pro) n.3973A>C | dbSNP |
| 13 | g.32338328A>G | CA387778940 | BRCA2 | c.3973A>G (p.Thr1325Ala) c.3604A>G (p.Thr1202Ala) n.3973A>G | ClinVar |
| 13 | g.32338328A>T | CA387778938 | BRCA2 | c.3973A>T (p.Thr1325Ser) c.3604A>T (p.Thr1202Ser) n.3973A>T | dbSNP |
| 13 | g.32338329C>A | CA387778942 | BRCA2 | c.3974C>A (p.Thr1325Asn) c.3605C>A (p.Thr1202Asn) n.3974C>A | |
| 13 | g.32338329C= | CA2082822617 | BRCA2 | c.3974C= (p.Thr1325=) c.3605C= (p.Thr1202=) n.3974C= | |
| 13 | g.32338329C>G | CA387778941 | BRCA2 | c.3974C>G (p.Thr1325Ser) c.3605C>G (p.Thr1202Ser) n.3974C>G | ClinVar dbSNP |
| 13 | g.32338329C>T | CA387778943 | BRCA2 | c.3974C>T (p.Thr1325Ile) c.3605C>T (p.Thr1202Ile) n.3974C>T | ClinVar dbSNP |
| 13 | g.32338330T>A | CA483437978 | BRCA2 | c.3975T>A (p.Thr1325=) c.3606T>A (p.Thr1202=) n.3975T>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338330T>C | CA16606681 | BRCA2 | c.3975T>C (p.Thr1325=) c.3606T>C (p.Thr1202=) n.3975T>C | ClinVar dbSNP |
| 13 | g.32338330T>G | CA483437977 | BRCA2 | c.3975T>G (p.Thr1325=) c.3606T>G (p.Thr1202=) n.3975T>G | |
| 13 | g.32338330T= | CA2082822624 | BRCA2 | c.3975T= (p.Thr1325=) c.3606T= (p.Thr1202=) n.3975T= | |
| 13 | g.32338330_32338333dup | CA019317 | BRCA2 | c.3975_3978dup (p.Ala1327CysfsTer4) c.3606_3609dup (p.Ala1204CysfsTer4) n.3975_3978dup | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338331G>A | CA387778944 | BRCA2 | c.3976G>A (p.Ala1326Thr) c.3607G>A (p.Ala1203Thr) n.3976G>A | dbSNP |
| 13 | g.32338331G>C | CA387778945 | BRCA2 | c.3976G>C (p.Ala1326Pro) c.3607G>C (p.Ala1203Pro) n.3976G>C | dbSNP |
| 13 | g.32338331G>T | CA387778946 | BRCA2 | c.3976G>T (p.Ala1326Ser) c.3607G>T (p.Ala1203Ser) n.3976G>T | dbSNP |
| 13 | g.32338332C>A | CA387778947 | BRCA2 | c.3977C>A (p.Ala1326Asp) c.3608C>A (p.Ala1203Asp) n.3977C>A | dbSNP |
| 13 | g.32338332C>G | CA387778948 | BRCA2 | c.3977C>G (p.Ala1326Gly) c.3608C>G (p.Ala1203Gly) n.3977C>G | dbSNP |
| 13 | g.32338332C>T | CA387778949 | BRCA2 | c.3977C>T (p.Ala1326Val) c.3608C>T (p.Ala1203Val) n.3977C>T | dbSNP |
| 13 | g.32338333T>A | CA483437981 | BRCA2 | c.3978T>A (p.Ala1326=) c.3609T>A (p.Ala1203=) n.3978T>A | dbSNP |
| 13 | g.32338333T>C | CA483437982 | BRCA2 | c.3978T>C (p.Ala1326=) c.3609T>C (p.Ala1203=) n.3978T>C | ClinVar gnomAD v4 |
| 13 | g.32338333T>G | CA483437983 | BRCA2 | c.3978T>G (p.Ala1326=) c.3609T>G (p.Ala1203=) n.3978T>G | dbSNP |
| 13 | g.32338333T= | CA2082822638 | BRCA2 | c.3978T= (p.Ala1326=) c.3609T= (p.Ala1203=) n.3978T= | |
| 13 | g.32338333_32338334insTTGC | CA10589236 | BRCA2 | c.3978_3979insTTGC (p.Ala1327LeufsTer4) c.3609_3610insTTGC (p.Ala1204LeufsTer4) n.3978_3979insTTGC | ClinVar dbSNP |
| 13 | g.32338334G>A | CA387778950 | BRCA2 | c.3979G>A (p.Ala1327Thr) c.3610G>A (p.Ala1204Thr) n.3979G>A | |
| 13 | g.32338334G>C | CA387778951 | BRCA2 | c.3979G>C (p.Ala1327Pro) c.3610G>C (p.Ala1204Pro) n.3979G>C | |
| 13 | g.32338334G= | CA2082822643 | BRCA2 | c.3979G= (p.Ala1327=) c.3610G= (p.Ala1204=) n.3979G= | |
| 13 | g.32338334G>T | CA387778952 | BRCA2 | c.3979G>T (p.Ala1327Ser) c.3610G>T (p.Ala1204Ser) n.3979G>T | ClinVar dbSNP |
| 13 | g.32338335C>A | CA387778955 | BRCA2 | c.3980C>A (p.Ala1327Asp) c.3611C>A (p.Ala1204Asp) n.3980C>A | dbSNP |
| 13 | g.32338335C>G | CA387778953 | BRCA2 | c.3980C>G (p.Ala1327Gly) c.3611C>G (p.Ala1204Gly) n.3980C>G | dbSNP |
| 13 | g.32338335C>T | CA387778954 | BRCA2 | c.3980C>T (p.Ala1327Val) c.3611C>T (p.Ala1204Val) n.3980C>T | dbSNP |
| 13 | g.32338336C>A | CA483437985 | BRCA2 | c.3981C>A (p.Ala1327=) c.3612C>A (p.Ala1204=) n.3981C>A | ClinVar dbSNP |
| 13 | g.32338336C= | CA2082822647 | BRCA2 | c.3981C= (p.Ala1327=) c.3612C= (p.Ala1204=) n.3981C= | |
| 13 | g.32338336C>G | CA483437986 | BRCA2 | c.3981C>G (p.Ala1327=) c.3612C>G (p.Ala1204=) n.3981C>G | dbSNP |
| 13 | g.32338336C>T | CA483437987 | BRCA2 | c.3981C>T (p.Ala1327=) c.3612C>T (p.Ala1204=) n.3981C>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338337A= | CA2082822656 | BRCA2 | c.3982A= (p.Ser1328=) c.3613A= (p.Ser1205=) n.3982A= | |
| 13 | g.32338337A>C | CA387778956 | BRCA2 | c.3982A>C (p.Ser1328Arg) c.3613A>C (p.Ser1205Arg) n.3982A>C | |
| 13 | g.32338337A>G | CA387778957 | BRCA2 | c.3982A>G (p.Ser1328Gly) c.3613A>G (p.Ser1205Gly) n.3982A>G | ClinVar dbSNP |
| 13 | g.32338337A>T | CA387778958 | BRCA2 | c.3982A>T (p.Ser1328Cys) c.3613A>T (p.Ser1205Cys) n.3982A>T | ClinVar dbSNP |
| 13 | g.32338338G>A | CA6940737 | BRCA2 | c.3983G>A (p.Ser1328Asn) c.3614G>A (p.Ser1205Asn) n.3983G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338338G>C | CA10579597 | BRCA2 | c.3983G>C (p.Ser1328Thr) c.3614G>C (p.Ser1205Thr) n.3983G>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338338G= | CA2082822663 | BRCA2 | c.3983G= (p.Ser1328=) c.3614G= (p.Ser1205=) n.3983G= | |
| 13 | g.32338338G>T | CA387778959 | BRCA2 | c.3983G>T (p.Ser1328Ile) c.3614G>T (p.Ser1205Ile) n.3983G>T | |
| 13 | g.32338339T>A | CA387778960 | BRCA2 | c.3984T>A (p.Ser1328Arg) c.3615T>A (p.Ser1205Arg) n.3984T>A | dbSNP |
| 13 | g.32338339T>C | CA10579598 | BRCA2 | c.3984T>C (p.Ser1328=) c.3615T>C (p.Ser1205=) n.3984T>C | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338339T>G | CA387778961 | BRCA2 | c.3984T>G (p.Ser1328Arg) c.3615T>G (p.Ser1205Arg) n.3984T>G | dbSNP |
| 13 | g.32338339T= | CA2082822681 | BRCA2 | c.3984T= (p.Ser1328=) c.3615T= (p.Ser1205=) n.3984T= | |
| 13 | g.32338340A= | CA2082822686 | BRCA2 | c.3985A= (p.Arg1329=) c.3616A= (p.Arg1206=) n.3985A= | |
| 13 | g.32338340A>C | CA483437994 | BRCA2 | c.3985A>C (p.Arg1329=) c.3616A>C (p.Arg1206=) n.3985A>C | |
| 13 | g.32338340A>G | CA019330 | BRCA2 | c.3985A>G (p.Arg1329Gly) c.3616A>G (p.Arg1206Gly) n.3985A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338340A>T | CA387778962 | BRCA2 | c.3985A>T (p.Arg1329Ter) c.3616A>T (p.Arg1206Ter) n.3985A>T | dbSNP |
| 13 | g.32338341G>A | CA387778965 | BRCA2 | c.3986G>A (p.Arg1329Lys) c.3617G>A (p.Arg1206Lys) n.3986G>A | ClinVar dbSNP |
| 13 | g.32338341G>C | CA387778964 | BRCA2 | c.3986G>C (p.Arg1329Thr) c.3617G>C (p.Arg1206Thr) n.3986G>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338341G= | CA2082822692 | BRCA2 | c.3986G= (p.Arg1329=) c.3617G= (p.Arg1206=) n.3986G= | |
| 13 | g.32338341G>T | CA387778963 | BRCA2 | c.3986G>T (p.Arg1329Ile) c.3617G>T (p.Arg1206Ile) n.3986G>T | ClinVar dbSNP |
| 13 | g.32338342A= | CA2082822698 | BRCA2 | c.3987A= (p.Arg1329=) c.3618A= (p.Arg1206=) n.3987A= | |
| 13 | g.32338342A>C | CA387778966 | BRCA2 | c.3987A>C (p.Arg1329Ser) c.3618A>C (p.Arg1206Ser) n.3987A>C | |
| 13 | g.32338342A>G | CA483437997 | BRCA2 | c.3987A>G (p.Arg1329=) c.3618A>G (p.Arg1206=) n.3987A>G | ClinVar |
| 13 | g.32338342A>T | CA019337 | BRCA2 | c.3987A>T (p.Arg1329Ser) c.3618A>T (p.Arg1206Ser) n.3987A>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338343A>C | CA387778967 | BRCA2 | c.3988A>C (p.Asn1330His) c.3619A>C (p.Asn1207His) n.3988A>C | ClinVar |
| 13 | g.32338343A>G | CA387778968 | BRCA2 | c.3988A>G (p.Asn1330Asp) c.3619A>G (p.Asn1207Asp) n.3988A>G | |
| 13 | g.32338343A>T | CA387778969 | BRCA2 | c.3988A>T (p.Asn1330Tyr) c.3619A>T (p.Asn1207Tyr) n.3988A>T | |
| 13 | g.32338344A= | CA2082822711 | BRCA2 | c.3989A= (p.Asn1330=) c.3620A= (p.Asn1207=) n.3989A= | |
| 13 | g.32338344A>C | CA387778970 | BRCA2 | c.3989A>C (p.Asn1330Thr) c.3620A>C (p.Asn1207Thr) n.3989A>C | |
| 13 | g.32338344A>G | CA16607464 | BRCA2 | c.3989A>G (p.Asn1330Ser) c.3620A>G (p.Asn1207Ser) n.3989A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338344A>T | CA387778971 | BRCA2 | c.3989A>T (p.Asn1330Ile) c.3620A>T (p.Asn1207Ile) n.3989A>T | ClinVar dbSNP |
| 13 | g.32338345T>A | CA387778972 | BRCA2 | c.3990T>A (p.Asn1330Lys) c.3621T>A (p.Asn1207Lys) n.3990T>A | |
| 13 | g.32338345T>C | CA483438001 | BRCA2 | c.3990T>C (p.Asn1330=) c.3621T>C (p.Asn1207=) n.3990T>C | |
| 13 | g.32338345T>G | CA387778973 | BRCA2 | c.3990T>G (p.Asn1330Lys) c.3621T>G (p.Asn1207Lys) n.3990T>G | dbSNP |
| 13 | g.32338346dup | CA2499222150 | BRCA2 | c.3991dup (p.Ser1331PhefsTer3) c.3622dup (p.Ser1208PhefsTer3) n.3991dup | ClinVar dbSNP |
| 13 | g.32338346T>A | CA387778974 | BRCA2 | c.3991T>A (p.Ser1331Thr) c.3622T>A (p.Ser1208Thr) n.3991T>A | ClinVar dbSNP |
| 13 | g.32338346T>C | CA387778975 | BRCA2 | c.3991T>C (p.Ser1331Pro) c.3622T>C (p.Ser1208Pro) n.3991T>C | dbSNP |
| 13 | g.32338346T>G | CA387778976 | BRCA2 | c.3991T>G (p.Ser1331Ala) c.3622T>G (p.Ser1208Ala) n.3991T>G | |
| 13 | g.32338347C>A | CA387778979 | BRCA2 | c.3992C>A (p.Ser1331Tyr) c.3623C>A (p.Ser1208Tyr) n.3992C>A | dbSNP |
| 13 | g.32338347C>G | CA387778977 | BRCA2 | c.3992C>G (p.Ser1331Cys) c.3623C>G (p.Ser1208Cys) n.3992C>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338347C>T | CA387778978 | BRCA2 | c.3992C>T (p.Ser1331Phe) c.3623C>T (p.Ser1208Phe) n.3992C>T | dbSNP |
| 13 | g.32338348T>A | CA483438006 | BRCA2 | c.3993T>A (p.Ser1331=) c.3624T>A (p.Ser1208=) n.3993T>A | dbSNP |
| 13 | g.32338348T>C | CA6940738 | BRCA2 | c.3993T>C (p.Ser1331=) c.3624T>C (p.Ser1208=) n.3993T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338348T>G | CA483438005 | BRCA2 | c.3993T>G (p.Ser1331=) c.3624T>G (p.Ser1208=) n.3993T>G | |
| 13 | g.32338348T= | CA2082822722 | BRCA2 | c.3993T= (p.Ser1331=) c.3624T= (p.Ser1208=) n.3993T= | |
| 13 | g.32338349C>A | CA387778980 | BRCA2 | c.3994C>A (p.His1332Asn) c.3625C>A (p.His1209Asn) n.3994C>A | dbSNP |
| 13 | g.32338349C= | CA2082822734 | BRCA2 | c.3994C= (p.His1332=) c.3625C= (p.His1209=) n.3994C= | |
| 13 | g.32338349C>G | CA16619701 | BRCA2 | c.3994C>G (p.His1332Asp) c.3625C>G (p.His1209Asp) n.3994C>G | ClinVar dbSNP |
| 13 | g.32338349C>T | CA336760 | BRCA2 | c.3994C>T (p.His1332Tyr) c.3625C>T (p.His1209Tyr) n.3994C>T | ClinVar dbSNP COSMIC COSMIC |
| 13 | g.32338350A= | CA2082822743 | BRCA2 | c.3995A= (p.His1332=) c.3626A= (p.His1209=) n.3995A= | |
| 13 | g.32338350A>C | CA387778981 | BRCA2 | c.3995A>C (p.His1332Pro) c.3626A>C (p.His1209Pro) n.3995A>C | |
| 13 | g.32338350A>G | CA019343 | BRCA2 | c.3995A>G (p.His1332Arg) c.3626A>G (p.His1209Arg) n.3995A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338350A>T | CA387778982 | BRCA2 | c.3995A>T (p.His1332Leu) c.3626A>T (p.His1209Leu) n.3995A>T | dbSNP |
| 13 | g.32338351T>A | CA387778983 | BRCA2 | c.3996T>A (p.His1332Gln) c.3627T>A (p.His1209Gln) n.3996T>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338351T>C | CA483438010 | BRCA2 | c.3996T>C (p.His1332=) c.3627T>C (p.His1209=) n.3996T>C | ClinVar dbSNP |
| 13 | g.32338351T>G | CA387778984 | BRCA2 | c.3996T>G (p.His1332Gln) c.3627T>G (p.His1209Gln) n.3996T>G | ClinVar dbSNP |
| 13 | g.32338351T= | CA2082822748 | BRCA2 | c.3996T= (p.His1332=) c.3627T= (p.His1209=) n.3996T= | |
| 13 | g.32338353_32338357del | CA2573149358 | BRCA2 | c.3998_4002del (p.Asn1333ArgfsTer3) c.3629_3633del (p.Asn1210ArgfsTer3) n.3998_4002del | ClinVar dbSNP |
| 13 | g.32338352A= | CA2082822758 | BRCA2 | c.3997A= (p.Asn1333=) c.3628A= (p.Asn1210=) n.3997A= | |
| 13 | g.32338352A>C | CA387778985 | BRCA2 | c.3997A>C (p.Asn1333His) c.3628A>C (p.Asn1210His) n.3997A>C | |
| 13 | g.32338352A>G | CA387778986 | BRCA2 | c.3997A>G (p.Asn1333Asp) c.3628A>G (p.Asn1210Asp) n.3997A>G | |
| 13 | g.32338352A>T | CA387778987 | BRCA2 | c.3997A>T (p.Asn1333Tyr) c.3628A>T (p.Asn1210Tyr) n.3997A>T | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338354_32338360del | CA2580087234 | BRCA2 | c.3999_4005del (p.Glu1335MetfsTer?) c.3630_3636del (p.Glu1212MetfsTer?) n.3999_4005del | ClinVar |
| 13 | g.32338353A>C | CA387778990 | BRCA2 | c.3998A>C (p.Asn1333Thr) c.3629A>C (p.Asn1210Thr) n.3998A>C | |
| 13 | g.32338353A>G | CA387778989 | BRCA2 | c.3998A>G (p.Asn1333Ser) c.3629A>G (p.Asn1210Ser) n.3998A>G | dbSNP |
| 13 | g.32338353A>T | CA387778988 | BRCA2 | c.3998A>T (p.Asn1333Ile) c.3629A>T (p.Asn1210Ile) n.3998A>T | dbSNP |
| 13 | g.32338354C>A | CA387778991 | BRCA2 | c.3999C>A (p.Asn1333Lys) c.3630C>A (p.Asn1210Lys) n.3999C>A | |
| 13 | g.32338354C= | CA2082822765 | BRCA2 | c.3999C= (p.Asn1333=) c.3630C= (p.Asn1210=) n.3999C= | |
| 13 | g.32338354C>G | CA019346 | BRCA2 | c.3999C>G (p.Asn1333Lys) c.3630C>G (p.Asn1210Lys) n.3999C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338354C>T | CA483438014 | BRCA2 | c.3999C>T (p.Asn1333=) c.3630C>T (p.Asn1210=) n.3999C>T | ClinVar gnomAD v4 |
| 13 | g.32338354_32338356delinsCTT | CA2082822773 | BRCA2 | c.3999_4001delinsCTT (p.Asn1333=) c.3630_3632delinsCTT (p.Asn1210=) n.3999_4001delinsCTT | |
| 13 | g.32338355T>A | CA387778992 | BRCA2 | c.4000T>A (p.Leu1334Ile) c.3631T>A (p.Leu1211Ile) n.4000T>A | dbSNP |
| 13 | g.32338355T>C | CA483438017 | BRCA2 | c.4000T>C (p.Leu1334=) c.3631T>C (p.Leu1211=) n.4000T>C | ClinVar dbSNP |
| 13 | g.32338355T>G | CA387778993 | BRCA2 | c.4000T>G (p.Leu1334Val) c.3631T>G (p.Leu1211Val) n.4000T>G | COSMIC COSMIC |
| 13 | g.32338355_32338356del | CA019371 | BRCA2 | c.4000_4001del (p.Leu1334ArgfsTer3) c.3631_3632del (p.Leu1211ArgfsTer3) n.4000_4001del | ClinVar dbSNP |
| 13 | g.32338357_32338362del | CA2825002134 | BRCA2 | c.4002_4007del (p.Leu1334_Glu1335del) c.3633_3638del (p.Leu1211_Glu1212del) n.4002_4007del | ClinVar |
| 13 | g.32338356T>A | CA019375 | BRCA2 | c.4001T>A (p.Leu1334Ter) c.3632T>A (p.Leu1211Ter) n.4001T>A | ClinVar dbSNP |
| 13 | g.32338356T>C | CA387778994 | BRCA2 | c.4001T>C (p.Leu1334Ser) c.3632T>C (p.Leu1211Ser) n.4001T>C | |
| 13 | g.32338356T>G | CA387778995 | BRCA2 | c.4001T>G (p.Leu1334Ter) c.3632T>G (p.Leu1211Ter) n.4001T>G | |
| 13 | g.32338356T= | CA2082822789 | BRCA2 | c.4001T= (p.Leu1334=) c.3632T= (p.Leu1211=) n.4001T= | |
| 13 | g.32338357A>C | CA387778996 | BRCA2 | c.4002A>C (p.Leu1334Phe) c.3633A>C (p.Leu1211Phe) n.4002A>C | |
| 13 | g.32338357A>G | CA483438018 | BRCA2 | c.4002A>G (p.Leu1334=) c.3633A>G (p.Leu1211=) n.4002A>G | dbSNP |
| 13 | g.32338357A>T | CA387778997 | BRCA2 | c.4002A>T (p.Leu1334Phe) c.3633A>T (p.Leu1211Phe) n.4002A>T | dbSNP |
| 13 | g.32338358G>A | CA387778998 | BRCA2 | c.4003G>A (p.Glu1335Lys) c.3634G>A (p.Glu1212Lys) n.4003G>A | |
| 13 | g.32338358G>C | CA387778999 | BRCA2 | c.4003G>C (p.Glu1335Gln) c.3634G>C (p.Glu1212Gln) n.4003G>C | |
| 13 | g.32338358G= | CA2082822803 | BRCA2 | c.4003G= (p.Glu1335=) c.3634G= (p.Glu1212=) n.4003G= | |
| 13 | g.32338358G>T | CA6940739 | BRCA2 | c.4003G>T (p.Glu1335Ter) c.3634G>T (p.Glu1212Ter) n.4003G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338359A= | CA2082822831 | BRCA2 | c.4004A= (p.Glu1335=) c.3635A= (p.Glu1212=) n.4004A= | |
| 13 | g.32338359A>C | CA387779002 | BRCA2 | c.4004A>C (p.Glu1335Ala) c.3635A>C (p.Glu1212Ala) n.4004A>C | |
| 13 | g.32338359A>G | CA387779000 | BRCA2 | c.4004A>G (p.Glu1335Gly) c.3635A>G (p.Glu1212Gly) n.4004A>G | ClinVar dbSNP |
| 13 | g.32338359A>T | CA387779001 | BRCA2 | c.4004A>T (p.Glu1335Val) c.3635A>T (p.Glu1212Val) n.4004A>T | dbSNP |
| 13 | g.32338360dup | CA019378 | BRCA2 | c.4005dup (p.Phe1336IlefsTer2) c.3636dup (p.Phe1213IlefsTer2) n.4005dup | ClinVar dbSNP |
| 13 | g.32338360A= | CA2082822841 | BRCA2 | c.4005A= (p.Glu1335=) c.3636A= (p.Glu1212=) n.4005A= | |
| 13 | g.32338360A>C | CA387779003 | BRCA2 | c.4005A>C (p.Glu1335Asp) c.3636A>C (p.Glu1212Asp) n.4005A>C | |
| 13 | g.32338360A>G | CA483438021 | BRCA2 | c.4005A>G (p.Glu1335=) c.3636A>G (p.Glu1212=) n.4005A>G | |
| 13 | g.32338360A>T | CA387779004 | BRCA2 | c.4005A>T (p.Glu1335Asp) c.3636A>T (p.Glu1212Asp) n.4005A>T | |
| 13 | g.32338361T>A | CA387779005 | BRCA2 | c.4006T>A (p.Phe1336Ile) c.3637T>A (p.Phe1213Ile) n.4006T>A | dbSNP |
| 13 | g.32338361T>C | CA387779006 | BRCA2 | c.4006T>C (p.Phe1336Leu) c.3637T>C (p.Phe1213Leu) n.4006T>C | dbSNP |
| 13 | g.32338361T>G | CA387779007 | BRCA2 | c.4006T>G (p.Phe1336Val) c.3637T>G (p.Phe1213Val) n.4006T>G | |
| 13 | g.32338361T= | CA2082822847 | BRCA2 | c.4006T= (p.Phe1336=) c.3637T= (p.Phe1213=) n.4006T= | |
| 13 | g.32338361_32338405dup | CA913188559 | BRCA2 | c.4006_4050dup (p.His1350_Lys1351insPheAspGlySerAspSerSerLysAsnAspThrValCysIleHis) c.3637_3681dup (p.His1227_Lys1228insPheAspGlySerAspSerSerLysAsnAspThrValCysIleHis) n.4006_4050dup | ClinVar dbSNP |
| 13 | g.32338361_32338362insA | CA019385 | BRCA2 | c.4006_4007insA (p.Phe1336TyrfsTer2) c.3637_3638insA (p.Phe1213TyrfsTer2) n.4006_4007insA | ClinVar dbSNP |
| 13 | g.32338361_32338362insCATC | CA658823560 | BRCA2 | c.4006_4007insCATC (p.Phe1336SerfsTer3) c.3637_3638insCATC (p.Phe1213SerfsTer3) n.4006_4007insCATC | ClinVar dbSNP |
| 13 | g.32338362T>A | CA387779008 | BRCA2 | c.4007T>A (p.Phe1336Tyr) c.3638T>A (p.Phe1213Tyr) n.4007T>A | ClinVar dbSNP |
| 13 | g.32338362T>C | CA6940740 | BRCA2 | c.4007T>C (p.Phe1336Ser) c.3638T>C (p.Phe1213Ser) n.4007T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338362T>G | CA387779009 | BRCA2 | c.4007T>G (p.Phe1336Cys) c.3638T>G (p.Phe1213Cys) n.4007T>G | |
| 13 | g.32338362T= | CA2082822872 | BRCA2 | c.4007T= (p.Phe1336=) c.3638T= (p.Phe1213=) n.4007T= | |
| 13 | g.32338362_32338363insCATC | CA10583098 | BRCA2 | c.4007_4008insCATC (p.Asp1337IlefsTer2) c.3638_3639insCATC (p.Asp1214IlefsTer2) n.4007_4008insCATC | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338363T>A | CA387779010 | BRCA2 | c.4008T>A (p.Phe1336Leu) c.3639T>A (p.Phe1213Leu) n.4008T>A | |
| 13 | g.32338363T>C | CA483438025 | BRCA2 | c.4008T>C (p.Phe1336=) c.3639T>C (p.Phe1213=) n.4008T>C | ClinVar dbSNP |
| 13 | g.32338363T>G | CA387779011 | BRCA2 | c.4008T>G (p.Phe1336Leu) c.3639T>G (p.Phe1213Leu) n.4008T>G | |
| 13 | g.32338363T= | CA2082822884 | BRCA2 | c.4008T= (p.Phe1336=) c.3639T= (p.Phe1213=) n.4008T= | |
| 13 | g.32338363_32338364insCATC | CA019388 | BRCA2 | c.4008_4009insCATC (p.Asp1337HisfsTer5) c.3639_3640insCATC (p.Asp1214HisfsTer5) n.4008_4009insCATC | ClinVar dbSNP |
| 13 | g.32338364G>A | CA387779014 | BRCA2 | c.4009G>A (p.Asp1337Asn) c.3640G>A (p.Asp1214Asn) n.4009G>A | dbSNP |
| 13 | g.32338364G>C | CA387779013 | BRCA2 | c.4009G>C (p.Asp1337His) c.3640G>C (p.Asp1214His) n.4009G>C | dbSNP |
| 13 | g.32338364G>T | CA387779012 | BRCA2 | c.4009G>T (p.Asp1337Tyr) c.3640G>T (p.Asp1214Tyr) n.4009G>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338365A= | CA2082822905 | BRCA2 | c.4010A= (p.Asp1337=) c.3641A= (p.Asp1214=) n.4010A= | |
| 13 | g.32338365A>C | CA387779015 | BRCA2 | c.4010A>C (p.Asp1337Ala) c.3641A>C (p.Asp1214Ala) n.4010A>C | ClinVar |
| 13 | g.32338365A>G | CA387779016 | BRCA2 | c.4010A>G (p.Asp1337Gly) c.3641A>G (p.Asp1214Gly) n.4010A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338365A>T | CA387779017 | BRCA2 | c.4010A>T (p.Asp1337Val) c.3641A>T (p.Asp1214Val) n.4010A>T | ClinVar dbSNP |
| 13 | g.32338366T>A | CA387779018 | BRCA2 | c.4011T>A (p.Asp1337Glu) c.3642T>A (p.Asp1214Glu) n.4011T>A | |
| 13 | g.32338366T>C | CA483438028 | BRCA2 | c.4011T>C (p.Asp1337=) c.3642T>C (p.Asp1214=) n.4011T>C | gnomAD v4 |
| 13 | g.32338366T>G | CA387779019 | BRCA2 | c.4011T>G (p.Asp1337Glu) c.3642T>G (p.Asp1214Glu) n.4011T>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338366T= | CA2082822918 | BRCA2 | c.4011T= (p.Asp1337=) c.3642T= (p.Asp1214=) n.4011T= | |
| 13 | g.32338366_32338367delinsTG | CA2082822911 | BRCA2 | c.4011_4012delinsTG (p.Asp1337=) c.3642_3643delinsTG (p.Asp1214=) n.4011_4012delinsTG | |
| 13 | g.32338367G>A | CA387779020 | BRCA2 | c.4012G>A (p.Gly1338Ser) c.3643G>A (p.Gly1215Ser) n.4012G>A | ClinVar dbSNP |
| 13 | g.32338367G>C | CA387779021 | BRCA2 | c.4012G>C (p.Gly1338Arg) c.3643G>C (p.Gly1215Arg) n.4012G>C | dbSNP |
| 13 | g.32338367G= | CA2082822933 | BRCA2 | c.4012G= (p.Gly1338=) c.3643G= (p.Gly1215=) n.4012G= | |
| 13 | g.32338367G>T | CA387779022 | BRCA2 | c.4012G>T (p.Gly1338Cys) c.3643G>T (p.Gly1215Cys) n.4012G>T | dbSNP gnomAD v4 |
| 13 | g.32338367_32338368dup | CA658823561 | BRCA2 | c.4012_4013dup (p.Ser1339AlafsTer?) c.3643_3644dup (p.Ser1216AlafsTer?) n.4012_4013dup | ClinVar dbSNP |
| 13 | g.32338368del | CA019392 | BRCA2 | c.4013del (p.Gly1338AlafsTer?) c.3644del (p.Gly1215AlafsTer?) n.4013del | ClinVar dbSNP |
| 13 | g.32338367_32338369delinsGGC | CA2082822942 | BRCA2 | c.4012_4014delinsGGC (p.Gly1338=) c.3643_3645delinsGGC (p.Gly1215=) n.4012_4014delinsGGC | |
| 13 | g.32338368G>A | CA387779023 | BRCA2 | c.4013G>A (p.Gly1338Asp) c.3644G>A (p.Gly1215Asp) n.4013G>A | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
| 13 | g.32338368G>C | CA387779024 | BRCA2 | c.4013G>C (p.Gly1338Ala) c.3644G>C (p.Gly1215Ala) n.4013G>C | dbSNP |
| 13 | g.32338368G>T | CA387779025 | BRCA2 | c.4013G>T (p.Gly1338Val) c.3644G>T (p.Gly1215Val) n.4013G>T | ClinVar dbSNP |
| 13 | g.32338368_32338369del | CA658656332 | BRCA2 | c.4013_4014del (p.Gly1338GlufsTer2) c.3644_3645del (p.Gly1215GlufsTer2) n.4013_4014del | ClinVar dbSNP |
| 13 | g.32338369C>A | CA483438036 | BRCA2 | c.4014C>A (p.Gly1338=) c.3645C>A (p.Gly1215=) n.4014C>A | dbSNP gnomAD v4 |
| 13 | g.32338369C= | CA2082822955 | BRCA2 | c.4014C= (p.Gly1338=) c.3645C= (p.Gly1215=) n.4014C= | |
| 13 | g.32338369C>G | CA483438033 | BRCA2 | c.4014C>G (p.Gly1338=) c.3645C>G (p.Gly1215=) n.4014C>G | dbSNP |
| 13 | g.32338369C>T | CA483438035 | BRCA2 | c.4014C>T (p.Gly1338=) c.3645C>T (p.Gly1215=) n.4014C>T | ClinVar dbSNP gnomAD v4 COSMIC |
| 13 | g.32338369_32338370insGG | CA019398 | BRCA2 | c.4014_4015insGG (p.Ser1339GlyfsTer?) c.3645_3646insGG (p.Ser1216GlyfsTer?) n.4014_4015insGG | ClinVar dbSNP |
| 13 | g.32338370A>C | CA387779028 | BRCA2 | c.4015A>C (p.Ser1339Arg) c.3646A>C (p.Ser1216Arg) n.4015A>C | ClinVar |
| 13 | g.32338370A>G | CA387779026 | BRCA2 | c.4015A>G (p.Ser1339Gly) c.3646A>G (p.Ser1216Gly) n.4015A>G | |
| 13 | g.32338370A>T | CA387779027 | BRCA2 | c.4015A>T (p.Ser1339Cys) c.3646A>T (p.Ser1216Cys) n.4015A>T | dbSNP |
| 13 | g.32338371G>A | CA387779029 | BRCA2 | c.4016G>A (p.Ser1339Asn) c.3647G>A (p.Ser1216Asn) n.4016G>A | dbSNP gnomAD v4 |
| 13 | g.32338371G>C | CA387779030 | BRCA2 | c.4016G>C (p.Ser1339Thr) c.3647G>C (p.Ser1216Thr) n.4016G>C | dbSNP |
| 13 | g.32338371G>T | CA387779031 | BRCA2 | c.4016G>T (p.Ser1339Ile) c.3647G>T (p.Ser1216Ile) n.4016G>T | ClinVar dbSNP |
| 13 | g.32338372T>A | CA387779032 | BRCA2 | c.4017T>A (p.Ser1339Arg) c.3648T>A (p.Ser1216Arg) n.4017T>A | dbSNP |
| 13 | g.32338372T>C | CA483438102 | BRCA2 | c.4017T>C (p.Ser1339=) c.3648T>C (p.Ser1216=) n.4017T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338372T>G | CA387779033 | BRCA2 | c.4017T>G (p.Ser1339Arg) c.3648T>G (p.Ser1216Arg) n.4017T>G | ClinVar dbSNP |
| 13 | g.32338372T= | CA2082822966 | BRCA2 | c.4017T= (p.Ser1339=) c.3648T= (p.Ser1216=) n.4017T= | |
| 13 | g.32338373G>A | CA387779036 | BRCA2 | c.4018G>A (p.Asp1340Asn) c.3649G>A (p.Asp1217Asn) n.4018G>A | dbSNP |
| 13 | g.32338373G>C | CA387779034 | BRCA2 | c.4018G>C (p.Asp1340His) c.3649G>C (p.Asp1217His) n.4018G>C | dbSNP |
| 13 | g.32338373G>T | CA387779035 | BRCA2 | c.4018G>T (p.Asp1340Tyr) c.3649G>T (p.Asp1217Tyr) n.4018G>T | gnomAD v4 |
| 13 | g.32338374A= | CA2082822988 | BRCA2 | c.4019A= (p.Asp1340=) c.3650A= (p.Asp1217=) n.4019A= | |
| 13 | g.32338374A>C | CA387779037 | BRCA2 | c.4019A>C (p.Asp1340Ala) c.3650A>C (p.Asp1217Ala) n.4019A>C | ClinVar dbSNP |
| 13 | g.32338374A>G | CA387779038 | BRCA2 | c.4019A>G (p.Asp1340Gly) c.3650A>G (p.Asp1217Gly) n.4019A>G | ClinVar dbSNP |
| 13 | g.32338374A>T | CA387779039 | BRCA2 | c.4019A>T (p.Asp1340Val) c.3650A>T (p.Asp1217Val) n.4019A>T | ClinVar dbSNP |
| 13 | g.32338374_32338375delinsAT | CA2082822977 | BRCA2 | c.4019_4020delinsAT (p.Asp1340=) c.3650_3651delinsAT (p.Asp1217=) n.4019_4020delinsAT | |
| 13 | g.32338375T>A | CA387779040 | BRCA2 | c.4020T>A (p.Asp1340Glu) c.3651T>A (p.Asp1217Glu) n.4020T>A | dbSNP |
| 13 | g.32338375T>C | CA483438104 | BRCA2 | c.4020T>C (p.Asp1340=) c.3651T>C (p.Asp1217=) n.4020T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338375T>G | CA387779041 | BRCA2 | c.4020T>G (p.Asp1340Glu) c.3651T>G (p.Asp1217Glu) n.4020T>G | dbSNP gnomAD v4 |
| 13 | g.32338375T= | CA2082823004 | BRCA2 | c.4020T= (p.Asp1340=) c.3651T= (p.Asp1217=) n.4020T= | |
| 13 | g.32338376dup | CA10589237 | BRCA2 | c.4021dup (p.Ser1341PhefsTer3) c.3652dup (p.Ser1218PhefsTer3) n.4021dup | ClinVar dbSNP |
| 13 | g.32338376del | CA019401 | BRCA2 | c.4021del (p.Ser1341GlnfsTer?) c.3652del (p.Ser1218GlnfsTer?) n.4021del | ClinVar dbSNP |
| 13 | g.32338376T>A | CA387779042 | BRCA2 | c.4021T>A (p.Ser1341Thr) c.3652T>A (p.Ser1218Thr) n.4021T>A | dbSNP |
| 13 | g.32338376T>C | CA387779043 | BRCA2 | c.4021T>C (p.Ser1341Pro) c.3652T>C (p.Ser1218Pro) n.4021T>C | ClinVar dbSNP |
| 13 | g.32338376T>G | CA387779044 | BRCA2 | c.4021T>G (p.Ser1341Ala) c.3652T>G (p.Ser1218Ala) n.4021T>G | |
| 13 | g.32338377del | CA2580087236 | BRCA2 | c.4022del (p.Ser1341Ter) c.3653del (p.Ser1218Ter) n.4022del | ClinVar |
| 13 | g.32338377C>A | CA387779046 | BRCA2 | c.4022C>A (p.Ser1341Ter) c.3653C>A (p.Ser1218Ter) n.4022C>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338377C= | CA2082823011 | BRCA2 | c.4022C= (p.Ser1341=) c.3653C= (p.Ser1218=) n.4022C= | |
| 13 | g.32338377C>G | CA387779045 | BRCA2 | c.4022C>G (p.Ser1341Ter) c.3653C>G (p.Ser1218Ter) n.4022C>G | ClinVar dbSNP COSMIC COSMIC |
| 13 | g.32338377C>T | CA387779047 | BRCA2 | c.4022C>T (p.Ser1341Leu) c.3653C>T (p.Ser1218Leu) n.4022C>T | dbSNP |
| 13 | g.32338378A= | CA2082823021 | BRCA2 | c.4023A= (p.Ser1341=) c.3654A= (p.Ser1218=) n.4023A= | |
| 13 | g.32338378A>C | CA019406 | BRCA2 | c.4023A>C (p.Ser1341=) c.3654A>C (p.Ser1218=) n.4023A>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338378A>G | CA483438106 | BRCA2 | c.4023A>G (p.Ser1341=) c.3654A>G (p.Ser1218=) n.4023A>G | dbSNP |
| 13 | g.32338378A>T | CA483438105 | BRCA2 | c.4023A>T (p.Ser1341=) c.3654A>T (p.Ser1218=) n.4023A>T | dbSNP |
| 13 | g.32338379A= | CA2082823030 | BRCA2 | c.4024A= (p.Ser1342=) c.3655A= (p.Ser1219=) n.4024A= | |
| 13 | g.32338379A>C | CA387779049 | BRCA2 | c.4024A>C (p.Ser1342Arg) c.3655A>C (p.Ser1219Arg) n.4024A>C | |
| 13 | g.32338379A>G | CA16614147 | BRCA2 | c.4024A>G (p.Ser1342Gly) c.3655A>G (p.Ser1219Gly) n.4024A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338379A>T | CA387779048 | BRCA2 | c.4024A>T (p.Ser1342Cys) c.3655A>T (p.Ser1219Cys) n.4024A>T | dbSNP |
| 13 | g.32338380G>A | CA387779050 | BRCA2 | c.4025G>A (p.Ser1342Asn) c.3656G>A (p.Ser1219Asn) n.4025G>A | ClinVar dbSNP |
| 13 | g.32338380G>C | CA387779051 | BRCA2 | c.4025G>C (p.Ser1342Thr) c.3656G>C (p.Ser1219Thr) n.4025G>C | dbSNP |
| 13 | g.32338380G= | CA2082823042 | BRCA2 | c.4025G= (p.Ser1342=) c.3656G= (p.Ser1219=) n.4025G= | |
| 13 | g.32338380G>T | CA387779052 | BRCA2 | c.4025G>T (p.Ser1342Ile) c.3656G>T (p.Ser1219Ile) n.4025G>T | ClinVar dbSNP |
| 13 | g.32338381del | CA2499222151 | BRCA2 | c.4026del (p.Ser1342ArgfsTer?) c.3657del (p.Ser1219ArgfsTer?) n.4026del | ClinVar dbSNP |
| 13 | g.32338381T>A | CA387779053 | BRCA2 | c.4026T>A (p.Ser1342Arg) c.3657T>A (p.Ser1219Arg) n.4026T>A | |
| 13 | g.32338381T>C | CA483438107 | BRCA2 | c.4026T>C (p.Ser1342=) c.3657T>C (p.Ser1219=) n.4026T>C | |
| 13 | g.32338381T>G | CA387779054 | BRCA2 | c.4026T>G (p.Ser1342Arg) c.3657T>G (p.Ser1219Arg) n.4026T>G | |
| 13 | g.32338381_32338382delinsTA | CA2082823057 | BRCA2 | c.4026_4027delinsTA (p.Ser1342=) c.3657_3658delinsTA (p.Ser1219=) n.4026_4027delinsTA | |
| 13 | g.32338382A= | CA2082823072 | BRCA2 | c.4027A= (p.Lys1343=) c.3658A= (p.Lys1220=) n.4027A= | |
| 13 | g.32338382A>C | CA387779055 | BRCA2 | c.4027A>C (p.Lys1343Gln) c.3658A>C (p.Lys1220Gln) n.4027A>C | |
| 13 | g.32338382A>G | CA019411 | BRCA2 | c.4027A>G (p.Lys1343Glu) c.3658A>G (p.Lys1220Glu) n.4027A>G | ClinVar dbSNP |
| 13 | g.32338382A>T | CA387779056 | BRCA2 | c.4027A>T (p.Lys1343Ter) c.3658A>T (p.Lys1220Ter) n.4027A>T | dbSNP |
| 13 | g.32338386del | CA609453792 | BRCA2 | c.4031del (p.Asn1344MetfsTer30) c.3662del (p.Asn1221MetfsTer30) n.4031del | ClinVar dbSNP gnomAD v2 |
| 13 | g.32338383A>C | CA387779057 | BRCA2 | c.4028A>C (p.Lys1343Thr) c.3659A>C (p.Lys1220Thr) n.4028A>C | |
| 13 | g.32338383A>G | CA387779058 | BRCA2 | c.4028A>G (p.Lys1343Arg) c.3659A>G (p.Lys1220Arg) n.4028A>G | ClinVar |
| 13 | g.32338383A>T | CA387779059 | BRCA2 | c.4028A>T (p.Lys1343Ile) c.3659A>T (p.Lys1220Ile) n.4028A>T | dbSNP |
| 13 | g.32338383_32338388delinsAAAATG | CA2082823080 | BRCA2 | c.4028_4033delinsAAAATG (p.Lys1343=) c.3659_3664delinsAAAATG (p.Lys1220=) n.4028_4033delinsAAAATG |