| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32337870C>A | CA16614291 | BRCA2 | c.3515C>A (p.Ser1172Ter) c.3146C>A (p.Ser1049Ter) n.3515C>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337870C= | CA2082818036 | BRCA2 | c.3515C= (p.Ser1172=) c.3146C= (p.Ser1049=) n.3515C= | |
| 13 | g.32337870C>G | CA018223 | BRCA2 | c.3515C>G (p.Ser1172Trp) c.3146C>G (p.Ser1049Trp) n.3515C>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337870C>T | CA018231 | BRCA2 | c.3515C>T (p.Ser1172Leu) c.3146C>T (p.Ser1049Leu) n.3515C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337871G>A | CA018238 | BRCA2 | c.3516G>A (p.Ser1172=) c.3147G>A (p.Ser1049=) n.3516G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337871G>C | CA483437593 | BRCA2 | c.3516G>C (p.Ser1172=) c.3147G>C (p.Ser1049=) n.3516G>C | dbSNP |
| 13 | g.32337871G= | CA2018046949 | BRCA2 | c.3516G= (p.Ser1172=) c.3147G= (p.Ser1049=) n.3516G= | |
| 13 | g.32337871G>T | CA10579580 | BRCA2 | c.3516G>T (p.Ser1172=) c.3147G>T (p.Ser1049=) n.3516G>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32337872A= | CA2082818055 | BRCA2 | c.3517A= (p.Ile1173=) c.3148A= (p.Ile1050=) n.3517A= | |
| 13 | g.32337872A>C | CA387777030 | BRCA2 | c.3517A>C (p.Ile1173Leu) c.3148A>C (p.Ile1050Leu) n.3517A>C | dbSNP |
| 13 | g.32337872A>G | CA387777031 | BRCA2 | c.3517A>G (p.Ile1173Val) c.3148A>G (p.Ile1050Val) n.3517A>G | ClinVar dbSNP |
| 13 | g.32337872A>T | CA018244 | BRCA2 | c.3517A>T (p.Ile1173Phe) c.3148A>T (p.Ile1050Phe) n.3517A>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32337873T>A | CA387777035 | BRCA2 | c.3518T>A (p.Ile1173Asn) c.3149T>A (p.Ile1050Asn) n.3518T>A | dbSNP |
| 13 | g.32337873T>C | CA018250 | BRCA2 | c.3518T>C (p.Ile1173Thr) c.3149T>C (p.Ile1050Thr) n.3518T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337873T>G | CA387777038 | BRCA2 | c.3518T>G (p.Ile1173Ser) c.3149T>G (p.Ile1050Ser) n.3518T>G | dbSNP |
| 13 | g.32337873T= | CA2082818060 | BRCA2 | c.3518T= (p.Ile1173=) c.3149T= (p.Ile1050=) n.3518T= | |
| 13 | g.32337874del | CA2499222134 | BRCA2 | c.3519del (p.Ile1173MetfsTer4) c.3150del (p.Ile1050MetfsTer4) n.3519del | |
| 13 | g.32337874T>A | CA483437594 | BRCA2 | c.3519T>A (p.Ile1173=) c.3150T>A (p.Ile1050=) n.3519T>A | dbSNP |
| 13 | g.32337874T>C | CA483437595 | BRCA2 | c.3519T>C (p.Ile1173=) c.3150T>C (p.Ile1050=) n.3519T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337874T>G | CA387777041 | BRCA2 | c.3519T>G (p.Ile1173Met) c.3150T>G (p.Ile1050Met) n.3519T>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337874T= | CA2082818068 | BRCA2 | c.3519T= (p.Ile1173=) c.3150T= (p.Ile1050=) n.3519T= | |
| 13 | g.32337874_32337878del | CA2695218186 | BRCA2 | c.3519_3523del (p.Gln1175ArgfsTer7) c.3150_3154del (p.Gln1052ArgfsTer7) n.3519_3523del | |
| 13 | g.32337875G>A | CA387777043 | BRCA2 | c.3520G>A (p.Gly1174Ser) c.3151G>A (p.Gly1051Ser) n.3520G>A | dbSNP |
| 13 | g.32337875G>C | CA387777046 | BRCA2 | c.3520G>C (p.Gly1174Arg) c.3151G>C (p.Gly1051Arg) n.3520G>C | dbSNP |
| 13 | g.32337875G>T | CA387777048 | BRCA2 | c.3520G>T (p.Gly1174Cys) c.3151G>T (p.Gly1051Cys) n.3520G>T | dbSNP |
| 13 | g.32337875_32337876insAATC | CA2499222135 | BRCA2 | c.3520_3521insAATC (p.Gly1174GlufsTer11) c.3151_3152insAATC (p.Gly1051GlufsTer11) n.3520_3521insAATC | |
| 13 | g.32337876G>A | CA387777051 | BRCA2 | c.3521G>A (p.Gly1174Asp) c.3152G>A (p.Gly1051Asp) n.3521G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337876G>C | CA387777052 | BRCA2 | c.3521G>C (p.Gly1174Ala) c.3152G>C (p.Gly1051Ala) n.3521G>C | dbSNP |
| 13 | g.32337876G= | CA2082818085 | BRCA2 | c.3521G= (p.Gly1174=) c.3152G= (p.Gly1051=) n.3521G= | |
| 13 | g.32337876G>T | CA387777054 | BRCA2 | c.3521G>T (p.Gly1174Val) c.3152G>T (p.Gly1051Val) n.3521G>T | ClinVar dbSNP |
| 13 | g.32337877T>A | CA483437596 | BRCA2 | c.3522T>A (p.Gly1174=) c.3153T>A (p.Gly1051=) n.3522T>A | |
| 13 | g.32337877T>C | CA483437597 | BRCA2 | c.3522T>C (p.Gly1174=) c.3153T>C (p.Gly1051=) n.3522T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337877T>G | CA483437598 | BRCA2 | c.3522T>G (p.Gly1174=) c.3153T>G (p.Gly1051=) n.3522T>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337877T= | CA2082818089 | BRCA2 | c.3522T= (p.Gly1174=) c.3153T= (p.Gly1051=) n.3522T= | |
| 13 | g.32337878C>A | CA387777056 | BRCA2 | c.3523C>A (p.Gln1175Lys) c.3154C>A (p.Gln1052Lys) n.3523C>A | ClinVar dbSNP |
| 13 | g.32337878C= | CA2082818098 | BRCA2 | c.3523C= (p.Gln1175=) c.3154C= (p.Gln1052=) n.3523C= | |
| 13 | g.32337878C>G | CA387777063 | BRCA2 | c.3523C>G (p.Gln1175Glu) c.3154C>G (p.Gln1052Glu) n.3523C>G | ClinVar dbSNP |
| 13 | g.32337878C>T | CA10589208 | BRCA2 | c.3523C>T (p.Gln1175Ter) c.3154C>T (p.Gln1052Ter) n.3523C>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337879A>C | CA387777064 | BRCA2 | c.3524A>C (p.Gln1175Pro) c.3155A>C (p.Gln1052Pro) n.3524A>C | |
| 13 | g.32337879A>G | CA387777066 | BRCA2 | c.3524A>G (p.Gln1175Arg) c.3155A>G (p.Gln1052Arg) n.3524A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337879A>T | CA387777068 | BRCA2 | c.3524A>T (p.Gln1175Leu) c.3155A>T (p.Gln1052Leu) n.3524A>T | dbSNP |
| 13 | g.32337880G>A | CA10579581 | BRCA2 | c.3525G>A (p.Gln1175=) c.3156G>A (p.Gln1052=) n.3525G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32337880G>C | CA387777071 | BRCA2 | c.3525G>C (p.Gln1175His) c.3156G>C (p.Gln1052His) n.3525G>C | dbSNP |
| 13 | g.32337880G= | CA2082818105 | BRCA2 | c.3525G= (p.Gln1175=) c.3156G= (p.Gln1052=) n.3525G= | |
| 13 | g.32337880G>T | CA387777074 | BRCA2 | c.3525G>T (p.Gln1175His) c.3156G>T (p.Gln1052His) n.3525G>T | |
| 13 | g.32337881G>A | CA018256 | BRCA2 | c.3526G>A (p.Val1176Ile) c.3157G>A (p.Val1053Ile) n.3526G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32337881G>C | CA387777078 | BRCA2 | c.3526G>C (p.Val1176Leu) c.3157G>C (p.Val1053Leu) n.3526G>C | dbSNP |
| 13 | g.32337881G= | CA2082818123 | BRCA2 | c.3526G= (p.Val1176=) c.3157G= (p.Val1053=) n.3526G= | |
| 13 | g.32337881G>T | CA387777079 | BRCA2 | c.3526G>T (p.Val1176Leu) c.3157G>T (p.Val1053Leu) n.3526G>T | dbSNP |
| 13 | g.32337882T>A | CA387777082 | BRCA2 | c.3527T>A (p.Val1176Glu) c.3158T>A (p.Val1053Glu) n.3527T>A | dbSNP |
| 13 | g.32337882T>C | CA387777088 | BRCA2 | c.3527T>C (p.Val1176Ala) c.3158T>C (p.Val1053Ala) n.3527T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337882T>G | CA387777089 | BRCA2 | c.3527T>G (p.Val1176Gly) c.3158T>G (p.Val1053Gly) n.3527T>G | dbSNP |
| 13 | g.32337882T= | CA2082818132 | BRCA2 | c.3527T= (p.Val1176=) c.3158T= (p.Val1053=) n.3527T= | |
| 13 | g.32337882_32337886delinsTAGAC | CA2082818130 | BRCA2 | c.3527_3531delinsTAGAC (p.Val1176=) c.3158_3162delinsTAGAC (p.Val1053=) n.3527_3531delinsTAGAC | |
| 13 | g.32337883A>C | CA483437599 | BRCA2 | c.3528A>C (p.Val1176=) c.3159A>C (p.Val1053=) n.3528A>C | |
| 13 | g.32337883A>G | CA483437600 | BRCA2 | c.3528A>G (p.Val1176=) c.3159A>G (p.Val1053=) n.3528A>G | |
| 13 | g.32337883A>T | CA483437601 | BRCA2 | c.3528A>T (p.Val1176=) c.3159A>T (p.Val1053=) n.3528A>T | dbSNP |
| 13 | g.32337885_32337888del | CA10589209 | BRCA2 | c.3530_3533del (p.Asp1177AlafsTer19) c.3161_3164del (p.Asp1054AlafsTer19) n.3530_3533del | ClinVar dbSNP |
| 13 | g.32337884G>A | CA16613951 | BRCA2 | c.3529G>A (p.Asp1177Asn) c.3160G>A (p.Asp1054Asn) n.3529G>A | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
| 13 | g.32337884G>C | CA387777097 | BRCA2 | c.3529G>C (p.Asp1177His) c.3160G>C (p.Asp1054His) n.3529G>C | dbSNP |
| 13 | g.32337884G= | CA2082818140 | BRCA2 | c.3529G= (p.Asp1177=) c.3160G= (p.Asp1054=) n.3529G= | |
| 13 | g.32337884G>T | CA387777095 | BRCA2 | c.3529G>T (p.Asp1177Tyr) c.3160G>T (p.Asp1054Tyr) n.3529G>T | dbSNP |
| 13 | g.32337884_32337886delinsGAC | CA2082818139 | BRCA2 | c.3529_3531delinsGAC (p.Asp1177=) c.3160_3162delinsGAC (p.Asp1054=) n.3529_3531delinsGAC | |
| 13 | g.32337885A= | CA2082818161 | BRCA2 | c.3530A= (p.Asp1177=) c.3161A= (p.Asp1054=) n.3530A= | |
| 13 | g.32337885A>C | CA6940702 | BRCA2 | c.3530A>C (p.Asp1177Ala) c.3161A>C (p.Asp1054Ala) n.3530A>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32337885A>G | CA387777101 | BRCA2 | c.3530A>G (p.Asp1177Gly) c.3161A>G (p.Asp1054Gly) n.3530A>G | |
| 13 | g.32337885A>T | CA387777104 | BRCA2 | c.3530A>T (p.Asp1177Val) c.3161A>T (p.Asp1054Val) n.3530A>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337886_32337887del | CA913188522 | BRCA2 | c.3531_3532del (p.Asp1177GlufsTer6) c.3162_3163del (p.Asp1054GlufsTer6) n.3531_3532del | ClinVar dbSNP |
| 13 | g.32337885_32337889delinsACAGC | CA2082818157 | BRCA2 | c.3530_3534delinsACAGC (p.Asp1177=) c.3161_3165delinsACAGC (p.Asp1054=) n.3530_3534delinsACAGC | |
| 13 | g.32337886C>A | CA387777107 | BRCA2 | c.3531C>A (p.Asp1177Glu) c.3162C>A (p.Asp1054Glu) n.3531C>A | dbSNP |
| 13 | g.32337886C= | CA2082818172 | BRCA2 | c.3531C= (p.Asp1177=) c.3162C= (p.Asp1054=) n.3531C= | |
| 13 | g.32337886C>G | CA387777109 | BRCA2 | c.3531C>G (p.Asp1177Glu) c.3162C>G (p.Asp1054Glu) n.3531C>G | dbSNP |
| 13 | g.32337886C>T | CA16606679 | BRCA2 | c.3531C>T (p.Asp1177=) c.3162C>T (p.Asp1054=) n.3531C>T | ClinVar dbSNP |
| 13 | g.32337886_32337889del | CA018270 | BRCA2 | c.3531_3534del (p.Asp1177GlufsTer19) c.3162_3165del (p.Asp1054GlufsTer19) n.3531_3534del | ClinVar dbSNP |
| 13 | g.32337887A= | CA2082818184 | BRCA2 | c.3532A= (p.Ser1178=) c.3163A= (p.Ser1055=) n.3532A= | |
| 13 | g.32337887A>C | CA387777113 | BRCA2 | c.3532A>C (p.Ser1178Arg) c.3163A>C (p.Ser1055Arg) n.3532A>C | |
| 13 | g.32337887A>G | CA018276 | BRCA2 | c.3532A>G (p.Ser1178Gly) c.3163A>G (p.Ser1055Gly) n.3532A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337887A>T | CA387777117 | BRCA2 | c.3532A>T (p.Ser1178Cys) c.3163A>T (p.Ser1055Cys) n.3532A>T | dbSNP |
| 13 | g.32337888G>A | CA387777119 | BRCA2 | c.3533G>A (p.Ser1178Asn) c.3164G>A (p.Ser1055Asn) n.3533G>A | dbSNP |
| 13 | g.32337888G>C | CA387777120 | BRCA2 | c.3533G>C (p.Ser1178Thr) c.3164G>C (p.Ser1055Thr) n.3533G>C | dbSNP |
| 13 | g.32337888G>T | CA387777123 | BRCA2 | c.3533G>T (p.Ser1178Ile) c.3164G>T (p.Ser1055Ile) n.3533G>T | |
| 13 | g.32337889C>A | CA387777125 | BRCA2 | c.3534C>A (p.Ser1178Arg) c.3165C>A (p.Ser1055Arg) n.3534C>A | dbSNP |
| 13 | g.32337889C= | CA2082818193 | BRCA2 | c.3534C= (p.Ser1178=) c.3165C= (p.Ser1055=) n.3534C= | |
| 13 | g.32337889C>G | CA387777126 | BRCA2 | c.3534C>G (p.Ser1178Arg) c.3165C>G (p.Ser1055Arg) n.3534C>G | dbSNP |
| 13 | g.32337889C>T | CA483437602 | BRCA2 | c.3534C>T (p.Ser1178=) c.3165C>T (p.Ser1055=) n.3534C>T | ClinVar dbSNP |
| 13 | g.32337889_32337893delinsCAGCA | CA2082818197 | BRCA2 | c.3534_3538delinsCAGCA (p.Ser1178=) c.3165_3169delinsCAGCA (p.Ser1055=) n.3534_3538delinsCAGCA | |
| 13 | g.32337890A>C | CA387777133 | BRCA2 | c.3535A>C (p.Ser1179Arg) c.3166A>C (p.Ser1056Arg) n.3535A>C | |
| 13 | g.32337890A>G | CA387777129 | BRCA2 | c.3535A>G (p.Ser1179Gly) c.3166A>G (p.Ser1056Gly) n.3535A>G | |
| 13 | g.32337890A>T | CA387777131 | BRCA2 | c.3535A>T (p.Ser1179Cys) c.3166A>T (p.Ser1056Cys) n.3535A>T | |
| 13 | g.32337895_32337898del | CA915948453 | BRCA2 | c.3540_3543del (p.Lys1180AsnfsTer16) c.3171_3174del (p.Lys1057AsnfsTer16) n.3540_3543del | ClinVar dbSNP |
| 13 | g.32337891G>A | CA018282 | BRCA2 | c.3536G>A (p.Ser1179Asn) c.3167G>A (p.Ser1056Asn) n.3536G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32337891G>C | CA387777137 | BRCA2 | c.3536G>C (p.Ser1179Thr) c.3167G>C (p.Ser1056Thr) n.3536G>C | dbSNP |
| 13 | g.32337891G= | CA2082818213 | BRCA2 | c.3536G= (p.Ser1179=) c.3167G= (p.Ser1056=) n.3536G= | |
| 13 | g.32337891G>T | CA387777138 | BRCA2 | c.3536G>T (p.Ser1179Ile) c.3167G>T (p.Ser1056Ile) n.3536G>T | |
| 13 | g.32337892C>A | CA387777141 | BRCA2 | c.3537C>A (p.Ser1179Arg) c.3168C>A (p.Ser1056Arg) n.3537C>A | |
| 13 | g.32337892C>G | CA387777142 | BRCA2 | c.3537C>G (p.Ser1179Arg) c.3168C>G (p.Ser1056Arg) n.3537C>G | |
| 13 | g.32337892C>T | CA483437603 | BRCA2 | c.3537C>T (p.Ser1179=) c.3168C>T (p.Ser1056=) n.3537C>T | |
| 13 | g.32337893A>C | CA387777145 | BRCA2 | c.3538A>C (p.Lys1180Gln) c.3169A>C (p.Lys1057Gln) n.3538A>C | |
| 13 | g.32337893A>G | CA387777148 | BRCA2 | c.3538A>G (p.Lys1180Glu) c.3169A>G (p.Lys1057Glu) n.3538A>G | ClinVar dbSNP |
| 13 | g.32337893A>T | CA387777150 | BRCA2 | c.3538A>T (p.Lys1180Ter) c.3169A>T (p.Lys1057Ter) n.3538A>T | ClinVar dbSNP |
| 13 | g.32337894A= | CA2082818218 | BRCA2 | c.3539A= (p.Lys1180=) c.3170A= (p.Lys1057=) n.3539A= | |
| 13 | g.32337894A>C | CA387777152 | BRCA2 | c.3539A>C (p.Lys1180Thr) c.3170A>C (p.Lys1057Thr) n.3539A>C | |
| 13 | g.32337894A>G | CA018286 | BRCA2 | c.3539A>G (p.Lys1180Arg) c.3170A>G (p.Lys1057Arg) n.3539A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 13 | g.32337894A>T | CA387777154 | BRCA2 | c.3539A>T (p.Lys1180Met) c.3170A>T (p.Lys1057Met) n.3539A>T | dbSNP |
| 13 | g.32337895G>A | CA483437604 | BRCA2 | c.3540G>A (p.Lys1180=) c.3171G>A (p.Lys1057=) n.3540G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337895G>C | CA350624 | BRCA2 | c.3540G>C (p.Lys1180Asn) c.3171G>C (p.Lys1057Asn) n.3540G>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32337895G= | CA2082818232 | BRCA2 | c.3540G= (p.Lys1180=) c.3171G= (p.Lys1057=) n.3540G= | |
| 13 | g.32337895G>T | CA387777157 | BRCA2 | c.3540G>T (p.Lys1180Asn) c.3171G>T (p.Lys1057Asn) n.3540G>T | ClinVar dbSNP |
| 13 | g.32337895_32337896delinsGC | CA2082818230 | BRCA2 | c.3540_3541delinsGC (p.Lys1180=) c.3171_3172delinsGC (p.Lys1057=) n.3540_3541delinsGC | |
| 13 | g.32337896del | CA919242465 | BRCA2 | c.3541del (p.Gln1181AsnfsTer16) c.3172del (p.Gln1058AsnfsTer16) n.3541del | dbSNP |
| 13 | g.32337896C>A | CA387777159 | BRCA2 | c.3541C>A (p.Gln1181Lys) c.3172C>A (p.Gln1058Lys) n.3541C>A | dbSNP |
| 13 | g.32337896C= | CA2082818245 | BRCA2 | c.3541C= (p.Gln1181=) c.3172C= (p.Gln1058=) n.3541C= | |
| 13 | g.32337896C>G | CA387777162 | BRCA2 | c.3541C>G (p.Gln1181Glu) c.3172C>G (p.Gln1058Glu) n.3541C>G | dbSNP |
| 13 | g.32337896C>T | CA247505295 | BRCA2 | c.3541C>T (p.Gln1181Ter) c.3172C>T (p.Gln1058Ter) n.3541C>T | dbSNP |
| 13 | g.32337897A>C | CA387777164 | BRCA2 | c.3542A>C (p.Gln1181Pro) c.3173A>C (p.Gln1058Pro) n.3542A>C | |
| 13 | g.32337897A>G | CA387777167 | BRCA2 | c.3542A>G (p.Gln1181Arg) c.3173A>G (p.Gln1058Arg) n.3542A>G | dbSNP |
| 13 | g.32337897A>T | CA387777168 | BRCA2 | c.3542A>T (p.Gln1181Leu) c.3173A>T (p.Gln1058Leu) n.3542A>T | |
| 13 | g.32337898A= | CA2082818268 | BRCA2 | c.3543A= (p.Gln1181=) c.3174A= (p.Gln1058=) n.3543A= | |
| 13 | g.32337898A>C | CA387777170 | BRCA2 | c.3543A>C (p.Gln1181His) c.3174A>C (p.Gln1058His) n.3543A>C | ClinVar dbSNP |
| 13 | g.32337898A>G | CA483437605 | BRCA2 | c.3543A>G (p.Gln1181=) c.3174A>G (p.Gln1058=) n.3543A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337898A>T | CA387777172 | BRCA2 | c.3543A>T (p.Gln1181His) c.3174A>T (p.Gln1058His) n.3543A>T | dbSNP |
| 13 | g.32337898_32337900delinsATT | CA2082818258 | BRCA2 | c.3543_3545delinsATT (p.Gln1181=) c.3174_3176delinsATT (p.Gln1058=) n.3543_3545delinsATT | |
| 13 | g.32337899T>A | CA387777179 | BRCA2 | c.3544T>A (p.Phe1182Ile) c.3175T>A (p.Phe1059Ile) n.3544T>A | dbSNP |
| 13 | g.32337899T>C | CA387777182 | BRCA2 | c.3544T>C (p.Phe1182Leu) c.3175T>C (p.Phe1059Leu) n.3544T>C | dbSNP |
| 13 | g.32337899T>G | CA387777184 | BRCA2 | c.3544T>G (p.Phe1182Val) c.3175T>G (p.Phe1059Val) n.3544T>G | dbSNP |
| 13 | g.32337901del | CA10589210 | BRCA2 | c.3546del (p.Phe1182LeufsTer15) c.3177del (p.Phe1059LeufsTer15) n.3546del | ClinVar dbSNP |
| 13 | g.32337900_32337901del | CA018299 | BRCA2 | c.3545_3546del (p.Phe1182Ter) c.3176_3177del (p.Phe1059Ter) n.3545_3546del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337900T>A | CA387777191 | BRCA2 | c.3545T>A (p.Phe1182Tyr) c.3176T>A (p.Phe1059Tyr) n.3545T>A | |
| 13 | g.32337900T>C | CA387777190 | BRCA2 | c.3545T>C (p.Phe1182Ser) c.3176T>C (p.Phe1059Ser) n.3545T>C | |
| 13 | g.32337900T>G | CA387777188 | BRCA2 | c.3545T>G (p.Phe1182Cys) c.3176T>G (p.Phe1059Cys) n.3545T>G | |
| 13 | g.32337901T>A | CA387777195 | BRCA2 | c.3546T>A (p.Phe1182Leu) c.3177T>A (p.Phe1059Leu) n.3546T>A | dbSNP |
| 13 | g.32337901T>C | CA483437606 | BRCA2 | c.3546T>C (p.Phe1182=) c.3177T>C (p.Phe1059=) n.3546T>C | dbSNP |
| 13 | g.32337901T>G | CA387777200 | BRCA2 | c.3546T>G (p.Phe1182Leu) c.3177T>G (p.Phe1059Leu) n.3546T>G | |
| 13 | g.32337902G>A | CA387777203 | BRCA2 | c.3547G>A (p.Glu1183Lys) c.3178G>A (p.Glu1060Lys) n.3547G>A | dbSNP |
| 13 | g.32337902G>C | CA387777204 | BRCA2 | c.3547G>C (p.Glu1183Gln) c.3178G>C (p.Glu1060Gln) n.3547G>C | ClinVar dbSNP |
| 13 | g.32337902G= | CA2082818288 | BRCA2 | c.3547G= (p.Glu1183=) c.3178G= (p.Glu1060=) n.3547G= | |
| 13 | g.32337902G>T | CA387777205 | BRCA2 | c.3547G>T (p.Glu1183Ter) c.3178G>T (p.Glu1060Ter) n.3547G>T | |
| 13 | g.32337903A>C | CA387777208 | BRCA2 | c.3548A>C (p.Glu1183Ala) c.3179A>C (p.Glu1060Ala) n.3548A>C | |
| 13 | g.32337903A>G | CA387777211 | BRCA2 | c.3548A>G (p.Glu1183Gly) c.3179A>G (p.Glu1060Gly) n.3548A>G | dbSNP |
| 13 | g.32337903A>T | CA387777212 | BRCA2 | c.3548A>T (p.Glu1183Val) c.3179A>T (p.Glu1060Val) n.3548A>T | dbSNP |
| 13 | g.32337904A>C | CA387777215 | BRCA2 | c.3549A>C (p.Glu1183Asp) c.3180A>C (p.Glu1060Asp) n.3549A>C | |
| 13 | g.32337904A>G | CA483437607 | BRCA2 | c.3549A>G (p.Glu1183=) c.3180A>G (p.Glu1060=) n.3549A>G | dbSNP |
| 13 | g.32337904A>T | CA387777217 | BRCA2 | c.3549A>T (p.Glu1183Asp) c.3180A>T (p.Glu1060Asp) n.3549A>T | dbSNP |
| 13 | g.32337905G>A | CA387777220 | BRCA2 | c.3550G>A (p.Gly1184Ser) c.3181G>A (p.Gly1061Ser) n.3550G>A | ClinVar dbSNP COSMIC COSMIC |
| 13 | g.32337905G>C | CA387777225 | BRCA2 | c.3550G>C (p.Gly1184Arg) c.3181G>C (p.Gly1061Arg) n.3550G>C | dbSNP |
| 13 | g.32337905G= | CA2082818289 | BRCA2 | c.3550G= (p.Gly1184=) c.3181G= (p.Gly1061=) n.3550G= | |
| 13 | g.32337905G>T | CA387777221 | BRCA2 | c.3550G>T (p.Gly1184Cys) c.3181G>T (p.Gly1061Cys) n.3550G>T | ClinVar dbSNP |
| 13 | g.32337906G>A | CA387777227 | BRCA2 | c.3551G>A (p.Gly1184Asp) c.3182G>A (p.Gly1061Asp) n.3551G>A | ClinVar dbSNP |
| 13 | g.32337906G>C | CA018307 | BRCA2 | c.3551G>C (p.Gly1184Ala) c.3182G>C (p.Gly1061Ala) n.3551G>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337906G= | CA2082818297 | BRCA2 | c.3551G= (p.Gly1184=) c.3182G= (p.Gly1061=) n.3551G= | |
| 13 | g.32337906G>T | CA387777229 | BRCA2 | c.3551G>T (p.Gly1184Val) c.3182G>T (p.Gly1061Val) n.3551G>T | |
| 13 | g.32337907T>A | CA483437608 | BRCA2 | c.3552T>A (p.Gly1184=) c.3183T>A (p.Gly1061=) n.3552T>A | dbSNP |
| 13 | g.32337907T>C | CA483437609 | BRCA2 | c.3552T>C (p.Gly1184=) c.3183T>C (p.Gly1061=) n.3552T>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32337907T>G | CA483437610 | BRCA2 | c.3552T>G (p.Gly1184=) c.3183T>G (p.Gly1061=) n.3552T>G | |
| 13 | g.32337907T= | CA2082818305 | BRCA2 | c.3552T= (p.Gly1184=) c.3183T= (p.Gly1061=) n.3552T= | |
| 13 | g.32337907_32337909delinsTAC | CA2082818304 | BRCA2 | c.3552_3554delinsTAC (p.Gly1184=) c.3183_3185delinsTAC (p.Gly1061=) n.3552_3554delinsTAC | |
| 13 | g.32337908A= | CA2082818317 | BRCA2 | c.3553A= (p.Thr1185=) c.3184A= (p.Thr1062=) n.3553A= | |
| 13 | g.32337908A>C | CA387777234 | BRCA2 | c.3553A>C (p.Thr1185Pro) c.3184A>C (p.Thr1062Pro) n.3553A>C | |
| 13 | g.32337908A>G | CA018312 | BRCA2 | c.3553A>G (p.Thr1185Ala) c.3184A>G (p.Thr1062Ala) n.3553A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337908A>T | CA387777237 | BRCA2 | c.3553A>T (p.Thr1185Ser) c.3184A>T (p.Thr1062Ser) n.3553A>T | |
| 13 | g.32337908dup | CA2573149323 | BRCA2 | c.3553dup (p.Thr1185AsnfsTer3) c.3184dup (p.Thr1062AsnfsTer3) n.3553dup | ClinVar dbSNP |
| 13 | g.32337909_32337910del | CA018315 | BRCA2 | c.3554_3555del (p.Thr1185SerfsTer2) c.3185_3186del (p.Thr1062SerfsTer2) n.3554_3555del | ClinVar dbSNP |
| 13 | g.32337908_32337918delinsACAGTTGAAAT | CA2082818319 | BRCA2 | c.3553_3563delinsACAGTTGAAAT (p.Thr1185=) c.3184_3194delinsACAGTTGAAAT (p.Thr1062=) n.3553_3563delinsACAGTTGAAAT | |
| 13 | g.32337909C>A | CA387777242 | BRCA2 | c.3554C>A (p.Thr1185Lys) c.3185C>A (p.Thr1062Lys) n.3554C>A | |
| 13 | g.32337909C= | CA2082818335 | BRCA2 | c.3554C= (p.Thr1185=) c.3185C= (p.Thr1062=) n.3554C= | |
| 13 | g.32337909C>G | CA387777246 | BRCA2 | c.3554C>G (p.Thr1185Arg) c.3185C>G (p.Thr1062Arg) n.3554C>G | |
| 13 | g.32337909C>T | CA387777248 | BRCA2 | c.3554C>T (p.Thr1185Ile) c.3185C>T (p.Thr1062Ile) n.3554C>T | ClinVar dbSNP |
| 13 | g.32337909_32337918del | CA018321 | BRCA2 | c.3554_3563del (p.Thr1185IlefsTer9) c.3185_3194del (p.Thr1062IlefsTer9) n.3554_3563del | ClinVar dbSNP |
| 13 | g.32337909_32337919delinsCAGTTGAAATT | CA2082818338 | BRCA2 | c.3554_3564delinsCAGTTGAAATT (p.Thr1185=) c.3185_3195delinsCAGTTGAAATT (p.Thr1062=) n.3554_3564delinsCAGTTGAAATT | |
| 13 | g.32337910A= | CA2082818355 | BRCA2 | c.3555A= (p.Thr1185=) c.3186A= (p.Thr1062=) n.3555A= | |
| 13 | g.32337910A>C | CA483437611 | BRCA2 | c.3555A>C (p.Thr1185=) c.3186A>C (p.Thr1062=) n.3555A>C | |
| 13 | g.32337910A>G | CA10579582 | BRCA2 | c.3555A>G (p.Thr1185=) c.3186A>G (p.Thr1062=) n.3555A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32337910A>T | CA483437612 | BRCA2 | c.3555A>T (p.Thr1185=) c.3186A>T (p.Thr1062=) n.3555A>T | ClinVar dbSNP |
| 13 | g.32337910_32337911delinsAG | CA2082818353 | BRCA2 | c.3555_3556delinsAG (p.Thr1185=) c.3186_3187delinsAG (p.Thr1062=) n.3555_3556delinsAG | |
| 13 | g.32337911_32337920del | CA018331 | BRCA2 | c.3556_3565del (p.Val1186AsnfsTer8) c.3187_3196del (p.Val1063AsnfsTer8) n.3556_3565del | ClinVar dbSNP |
| 13 | g.32337911G>A | CA018342 | BRCA2 | c.3556G>A (p.Val1186Ile) c.3187G>A (p.Val1063Ile) n.3556G>A | ClinVar dbSNP |
| 13 | g.32337911G>C | CA387777255 | BRCA2 | c.3556G>C (p.Val1186Leu) c.3187G>C (p.Val1063Leu) n.3556G>C | dbSNP |
| 13 | g.32337911G= | CA2082818372 | BRCA2 | c.3556G= (p.Val1186=) c.3187G= (p.Val1063=) n.3556G= | |
| 13 | g.32337911G>T | CA387777256 | BRCA2 | c.3556G>T (p.Val1186Phe) c.3187G>T (p.Val1063Phe) n.3556G>T | |
| 13 | g.32337911delinsTTACAA | CA915948454 | BRCA2 | c.3556delinsTTACAA (p.Val1186LeufsTer13) c.3187delinsTTACAA (p.Val1063LeufsTer13) n.3556delinsTTACAA | ClinVar dbSNP |
| 13 | g.32337912T>A | CA387777259 | BRCA2 | c.3557T>A (p.Val1186Asp) c.3188T>A (p.Val1063Asp) n.3557T>A | ClinVar dbSNP |
| 13 | g.32337912T>C | CA6940703 | BRCA2 | c.3557T>C (p.Val1186Ala) c.3188T>C (p.Val1063Ala) n.3557T>C | dbSNP ExAC gnomAD v2 |
| 13 | g.32337912T>G | CA387777263 | BRCA2 | c.3557T>G (p.Val1186Gly) c.3188T>G (p.Val1063Gly) n.3557T>G | |
| 13 | g.32337912T= | CA2082818381 | BRCA2 | c.3557T= (p.Val1186=) c.3188T= (p.Val1063=) n.3557T= | |
| 13 | g.32337913T>A | CA483437613 | BRCA2 | c.3558T>A (p.Val1186=) c.3189T>A (p.Val1063=) n.3558T>A | dbSNP |
| 13 | g.32337913T>C | CA483437615 | BRCA2 | c.3558T>C (p.Val1186=) c.3189T>C (p.Val1063=) n.3558T>C | ClinVar dbSNP |
| 13 | g.32337913T>G | CA483437614 | BRCA2 | c.3558T>G (p.Val1186=) c.3189T>G (p.Val1063=) n.3558T>G | dbSNP |
| 13 | g.32337913T= | CA2082818390 | BRCA2 | c.3558T= (p.Val1186=) c.3189T= (p.Val1063=) n.3558T= | |
| 13 | g.32337914G>A | CA387777270 | BRCA2 | c.3559G>A (p.Glu1187Lys) c.3190G>A (p.Glu1064Lys) n.3559G>A | dbSNP |
| 13 | g.32337914G>C | CA387777268 | BRCA2 | c.3559G>C (p.Glu1187Gln) c.3190G>C (p.Glu1064Gln) n.3559G>C | dbSNP |
| 13 | g.32337914G= | CA2082818399 | BRCA2 | c.3559G= (p.Glu1187=) c.3190G= (p.Glu1064=) n.3559G= | |
| 13 | g.32337914G>T | CA387777265 | BRCA2 | c.3559G>T (p.Glu1187Ter) c.3190G>T (p.Glu1064Ter) n.3559G>T | dbSNP |
| 13 | g.32337915A>C | CA387777273 | BRCA2 | c.3560A>C (p.Glu1187Ala) c.3191A>C (p.Glu1064Ala) n.3560A>C | ClinVar |
| 13 | g.32337915A>G | CA387777275 | BRCA2 | c.3560A>G (p.Glu1187Gly) c.3191A>G (p.Glu1064Gly) n.3560A>G | dbSNP |
| 13 | g.32337915A>T | CA387777277 | BRCA2 | c.3560A>T (p.Glu1187Val) c.3191A>T (p.Glu1064Val) n.3560A>T | dbSNP |
| 13 | g.32337916A>C | CA387777279 | BRCA2 | c.3561A>C (p.Glu1187Asp) c.3192A>C (p.Glu1064Asp) n.3561A>C | |
| 13 | g.32337916A>G | CA483437616 | BRCA2 | c.3561A>G (p.Glu1187=) c.3192A>G (p.Glu1064=) n.3561A>G | dbSNP |
| 13 | g.32337916A>T | CA387777282 | BRCA2 | c.3561A>T (p.Glu1187Asp) c.3192A>T (p.Glu1064Asp) n.3561A>T | |
| 13 | g.32337917A= | CA2082818406 | BRCA2 | c.3562A= (p.Ile1188=) c.3193A= (p.Ile1065=) n.3562A= | |
| 13 | g.32337917A>C | CA387777284 | BRCA2 | c.3562A>C (p.Ile1188Leu) c.3193A>C (p.Ile1065Leu) n.3562A>C | |
| 13 | g.32337917A>G | CA018345 | BRCA2 | c.3562A>G (p.Ile1188Val) c.3193A>G (p.Ile1065Val) n.3562A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337917A>T | CA387777290 | BRCA2 | c.3562A>T (p.Ile1188Phe) c.3193A>T (p.Ile1065Phe) n.3562A>T | |
| 13 | g.32337918T>A | CA387777292 | BRCA2 | c.3563T>A (p.Ile1188Asn) c.3194T>A (p.Ile1065Asn) n.3563T>A | dbSNP |
| 13 | g.32337918T>C | CA387777295 | BRCA2 | c.3563T>C (p.Ile1188Thr) c.3194T>C (p.Ile1065Thr) n.3563T>C | ClinVar dbSNP |
| 13 | g.32337918T>G | CA387777296 | BRCA2 | c.3563T>G (p.Ile1188Ser) c.3194T>G (p.Ile1065Ser) n.3563T>G | |
| 13 | g.32337918_32337922delinsTTAAA | CA2082818415 | BRCA2 | c.3563_3567delinsTTAAA (p.Ile1188=) c.3194_3198delinsTTAAA (p.Ile1065=) n.3563_3567delinsTTAAA | |
| 13 | g.32337919T>A | CA483437618 | BRCA2 | c.3564T>A (p.Ile1188=) c.3195T>A (p.Ile1065=) n.3564T>A | |
| 13 | g.32337919T>C | CA483437617 | BRCA2 | c.3564T>C (p.Ile1188=) c.3195T>C (p.Ile1065=) n.3564T>C | ClinVar |
| 13 | g.32337919T>G | CA387777301 | BRCA2 | c.3564T>G (p.Ile1188Met) c.3195T>G (p.Ile1065Met) n.3564T>G | |
| 13 | g.32337919_32337922del | CA10589211 | BRCA2 | c.3564_3567del (p.Lys1189GlyfsTer7) c.3195_3198del (p.Lys1066GlyfsTer7) n.3564_3567del | ClinVar dbSNP |
| 13 | g.32337920A>C | CA387777303 | BRCA2 | c.3565A>C (p.Lys1189Gln) c.3196A>C (p.Lys1066Gln) n.3565A>C | |
| 13 | g.32337920A>G | CA387777306 | BRCA2 | c.3565A>G (p.Lys1189Glu) c.3196A>G (p.Lys1066Glu) n.3565A>G | dbSNP |
| 13 | g.32337920A>T | CA387777307 | BRCA2 | c.3565A>T (p.Lys1189Ter) c.3196A>T (p.Lys1066Ter) n.3565A>T | dbSNP |
| 13 | g.32337922dup | CA2695199695 | BRCA2 | c.3567dup (p.Arg1190ThrfsTer10) c.3198dup (p.Arg1067ThrfsTer10) n.3567dup | ClinVar |
| 13 | g.32337921A= | CA2082818429 | BRCA2 | c.3566A= (p.Lys1189=) c.3197A= (p.Lys1066=) n.3566A= | |
| 13 | g.32337921A>C | CA387777309 | BRCA2 | c.3566A>C (p.Lys1189Thr) c.3197A>C (p.Lys1066Thr) n.3566A>C | ClinVar dbSNP |
| 13 | g.32337921A>G | CA387777312 | BRCA2 | c.3566A>G (p.Lys1189Arg) c.3197A>G (p.Lys1066Arg) n.3566A>G | dbSNP |
| 13 | g.32337921A>T | CA387777314 | BRCA2 | c.3566A>T (p.Lys1189Ile) c.3197A>T (p.Lys1066Ile) n.3566A>T | ClinVar dbSNP |
| 13 | g.32337922A>C | CA387777319 | BRCA2 | c.3567A>C (p.Lys1189Asn) c.3198A>C (p.Lys1066Asn) n.3567A>C | |
| 13 | g.32337922A>G | CA483437619 | BRCA2 | c.3567A>G (p.Lys1189=) c.3198A>G (p.Lys1066=) n.3567A>G | ClinVar dbSNP |
| 13 | g.32337922A>T | CA387777317 | BRCA2 | c.3567A>T (p.Lys1189Asn) c.3198A>T (p.Lys1066Asn) n.3567A>T | dbSNP |
| 13 | g.32337923del | CA2580087093 | BRCA2 | c.3568del (p.Arg1190GlyfsTer7) c.3199del (p.Arg1067GlyfsTer7) n.3568del | ClinVar |
| 13 | g.32337923C>A | CA483437620 | BRCA2 | c.3568C>A (p.Arg1190=) c.3199C>A (p.Arg1067=) n.3568C>A | dbSNP |
| 13 | g.32337923C= | CA2082818435 | BRCA2 | c.3568C= (p.Arg1190=) c.3199C= (p.Arg1067=) n.3568C= | |
| 13 | g.32337923C>G | CA387777321 | BRCA2 | c.3568C>G (p.Arg1190Gly) c.3199C>G (p.Arg1067Gly) n.3568C>G | dbSNP |
| 13 | g.32337923C>T | CA018352 | BRCA2 | c.3568C>T (p.Arg1190Trp) c.3199C>T (p.Arg1067Trp) n.3568C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 13 | g.32337923_32337924delinsCG | CA2082818441 | BRCA2 | c.3568_3569delinsCG (p.Arg1190=) c.3199_3200delinsCG (p.Arg1067=) n.3568_3569delinsCG | |
| 13 | g.32337924G>A | CA018360 | BRCA2 | c.3569G>A (p.Arg1190Gln) c.3200G>A (p.Arg1067Gln) n.3569G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337924G>C | CA387777326 | BRCA2 | c.3569G>C (p.Arg1190Pro) c.3200G>C (p.Arg1067Pro) n.3569G>C | dbSNP |
| 13 | g.32337924G= | CA2082818453 | BRCA2 | c.3569G= (p.Arg1190=) c.3200G= (p.Arg1067=) n.3569G= | |
| 13 | g.32337924G>T | CA387777328 | BRCA2 | c.3569G>T (p.Arg1190Leu) c.3200G>T (p.Arg1067Leu) n.3569G>T | ClinVar dbSNP |
| 13 | g.32337925dup | CA2695218187 | BRCA2 | c.3570dup (p.Lys1191GlufsTer9) c.3201dup (p.Lys1068GlufsTer9) n.3570dup | |
| 13 | g.32337925del | CA018365 | BRCA2 | c.3570del (p.Lys1191SerfsTer6) c.3201del (p.Lys1068SerfsTer6) n.3570del | ClinVar dbSNP |
| 13 | g.32337925G>A | CA483437621 | BRCA2 | c.3570G>A (p.Arg1190=) c.3201G>A (p.Arg1067=) n.3570G>A | ClinVar dbSNP |
| 13 | g.32337925G>C | CA483437622 | BRCA2 | c.3570G>C (p.Arg1190=) c.3201G>C (p.Arg1067=) n.3570G>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337925G= | CA2082818466 | BRCA2 | c.3570G= (p.Arg1190=) c.3201G= (p.Arg1067=) n.3570G= | |
| 13 | g.32337925G>T | CA483437623 | BRCA2 | c.3570G>T (p.Arg1190=) c.3201G>T (p.Arg1067=) n.3570G>T | dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
| 13 | g.32337926A>C | CA387777331 | BRCA2 | c.3571A>C (p.Lys1191Gln) c.3202A>C (p.Lys1068Gln) n.3571A>C | |
| 13 | g.32337926A>G | CA387777334 | BRCA2 | c.3571A>G (p.Lys1191Glu) c.3202A>G (p.Lys1068Glu) n.3571A>G | |
| 13 | g.32337926A>T | CA387777333 | BRCA2 | c.3571A>T (p.Lys1191Ter) c.3202A>T (p.Lys1068Ter) n.3571A>T | |
| 13 | g.32337927del | CA2499222136 | BRCA2 | c.3572del (p.Lys1191SerfsTer6) c.3203del (p.Lys1068SerfsTer6) n.3572del | ClinVar |
| 13 | g.32337927A= | CA2082818476 | BRCA2 | c.3572A= (p.Lys1191=) c.3203A= (p.Lys1068=) n.3572A= | |
| 13 | g.32337927A>C | CA387777337 | BRCA2 | c.3572A>C (p.Lys1191Thr) c.3203A>C (p.Lys1068Thr) n.3572A>C | |
| 13 | g.32337927A>G | CA387777339 | BRCA2 | c.3572A>G (p.Lys1191Arg) c.3203A>G (p.Lys1068Arg) n.3572A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337927A>T | CA387777341 | BRCA2 | c.3572A>T (p.Lys1191Met) c.3203A>T (p.Lys1068Met) n.3572A>T | dbSNP |
| 13 | g.32337928G>A | CA483437624 | BRCA2 | c.3573G>A (p.Lys1191=) c.3204G>A (p.Lys1068=) n.3573G>A | ClinVar dbSNP |
| 13 | g.32337928G>C | CA387777344 | BRCA2 | c.3573G>C (p.Lys1191Asn) c.3204G>C (p.Lys1068Asn) n.3573G>C | dbSNP COSMIC COSMIC |
| 13 | g.32337928G= | CA2082818488 | BRCA2 | c.3573G= (p.Lys1191=) c.3204G= (p.Lys1068=) n.3573G= | |
| 13 | g.32337928G>T | CA387777346 | BRCA2 | c.3573G>T (p.Lys1191Asn) c.3204G>T (p.Lys1068Asn) n.3573G>T | |
| 13 | g.32337929T>A | CA387777349 | BRCA2 | c.3574T>A (p.Phe1192Ile) c.3205T>A (p.Phe1069Ile) n.3574T>A | dbSNP |
| 13 | g.32337929T>C | CA387777351 | BRCA2 | c.3574T>C (p.Phe1192Leu) c.3205T>C (p.Phe1069Leu) n.3574T>C | dbSNP |
| 13 | g.32337929T>G | CA387777353 | BRCA2 | c.3574T>G (p.Phe1192Val) c.3205T>G (p.Phe1069Val) n.3574T>G | dbSNP |
| 13 | g.32337930T>A | CA387777356 | BRCA2 | c.3575T>A (p.Phe1192Tyr) c.3206T>A (p.Phe1069Tyr) n.3575T>A | dbSNP |
| 13 | g.32337930T>C | CA387777358 | BRCA2 | c.3575T>C (p.Phe1192Ser) c.3206T>C (p.Phe1069Ser) n.3575T>C | |
| 13 | g.32337930T>G | CA018368 | BRCA2 | c.3575T>G (p.Phe1192Cys) c.3206T>G (p.Phe1069Cys) n.3575T>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 13 | g.32337930T= | CA2082818503 | BRCA2 | c.3575T= (p.Phe1192=) c.3206T= (p.Phe1069=) n.3575T= | |
| 13 | g.32337931T>A | CA387777361 | BRCA2 | c.3576T>A (p.Phe1192Leu) c.3207T>A (p.Phe1069Leu) n.3576T>A | ClinVar dbSNP |
| 13 | g.32337931T>C | CA483437626 | BRCA2 | c.3576T>C (p.Phe1192=) c.3207T>C (p.Phe1069=) n.3576T>C | |
| 13 | g.32337931T>G | CA387777363 | BRCA2 | c.3576T>G (p.Phe1192Leu) c.3207T>G (p.Phe1069Leu) n.3576T>G | |
| 13 | g.32337932G>A | CA387777366 | BRCA2 | c.3577G>A (p.Ala1193Thr) c.3208G>A (p.Ala1070Thr) n.3577G>A | ClinVar dbSNP |
| 13 | g.32337932G>C | CA387777368 | BRCA2 | c.3577G>C (p.Ala1193Pro) c.3208G>C (p.Ala1070Pro) n.3577G>C | dbSNP gnomAD v4 |
| 13 | g.32337932G= | CA2082818515 | BRCA2 | c.3577G= (p.Ala1193=) c.3208G= (p.Ala1070=) n.3577G= | |
| 13 | g.32337932G>T | CA387777371 | BRCA2 | c.3577G>T (p.Ala1193Ser) c.3208G>T (p.Ala1070Ser) n.3577G>T | ClinVar dbSNP |
| 13 | g.32337933C>A | CA387777373 | BRCA2 | c.3578C>A (p.Ala1193Asp) c.3209C>A (p.Ala1070Asp) n.3578C>A | |
| 13 | g.32337933C= | CA2082818524 | BRCA2 | c.3578C= (p.Ala1193=) c.3209C= (p.Ala1070=) n.3578C= | |
| 13 | g.32337933C>G | CA387777375 | BRCA2 | c.3578C>G (p.Ala1193Gly) c.3209C>G (p.Ala1070Gly) n.3578C>G | dbSNP |
| 13 | g.32337933C>T | CA018374 | BRCA2 | c.3578C>T (p.Ala1193Val) c.3209C>T (p.Ala1070Val) n.3578C>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337934T>A | CA483437630 | BRCA2 | c.3579T>A (p.Ala1193=) c.3210T>A (p.Ala1070=) n.3579T>A | |
| 13 | g.32337934T>C | CA483437628 | BRCA2 | c.3579T>C (p.Ala1193=) c.3210T>C (p.Ala1070=) n.3579T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337934T>G | CA483437629 | BRCA2 | c.3579T>G (p.Ala1193=) c.3210T>G (p.Ala1070=) n.3579T>G | |
| 13 | g.32337934T= | CA2082818533 | BRCA2 | c.3579T= (p.Ala1193=) c.3210T= (p.Ala1070=) n.3579T= | |
| 13 | g.32337935G>A | CA387777383 | BRCA2 | c.3580G>A (p.Gly1194Ser) c.3211G>A (p.Gly1071Ser) n.3580G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337935G>C | CA387777381 | BRCA2 | c.3580G>C (p.Gly1194Arg) c.3211G>C (p.Gly1071Arg) n.3580G>C | dbSNP |
| 13 | g.32337935G>T | CA387777379 | BRCA2 | c.3580G>T (p.Gly1194Cys) c.3211G>T (p.Gly1071Cys) n.3580G>T | dbSNP |
| 13 | g.32337936G>A | CA018377 | BRCA2 | c.3581G>A (p.Gly1194Asp) c.3212G>A (p.Gly1071Asp) n.3581G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337936G>C | CA387777386 | BRCA2 | c.3581G>C (p.Gly1194Ala) c.3212G>C (p.Gly1071Ala) n.3581G>C | dbSNP |
| 13 | g.32337936G= | CA2082818540 | BRCA2 | c.3581G= (p.Gly1194=) c.3212G= (p.Gly1071=) n.3581G= | |
| 13 | g.32337936G>T | CA387777389 | BRCA2 | c.3581G>T (p.Gly1194Val) c.3212G>T (p.Gly1071Val) n.3581G>T | dbSNP |
| 13 | g.32337937C>A | CA483437633 | BRCA2 | c.3582C>A (p.Gly1194=) c.3213C>A (p.Gly1071=) n.3582C>A | dbSNP |
| 13 | g.32337937C= | CA2082818557 | BRCA2 | c.3582C= (p.Gly1194=) c.3213C= (p.Gly1071=) n.3582C= | |
| 13 | g.32337937C>G | CA6940704 | BRCA2 | c.3582C>G (p.Gly1194=) c.3213C>G (p.Gly1071=) n.3582C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32337937C>T | CA483437634 | BRCA2 | c.3582C>T (p.Gly1194=) c.3213C>T (p.Gly1071=) n.3582C>T | ClinVar dbSNP |
| 13 | g.32337938C>A | CA10583091 | BRCA2 | c.3583C>A (p.Leu1195Met) c.3214C>A (p.Leu1072Met) n.3583C>A | ClinVar dbSNP |
| 13 | g.32337938C= | CA2082818562 | BRCA2 | c.3583C= (p.Leu1195=) c.3214C= (p.Leu1072=) n.3583C= | |
| 13 | g.32337938C>G | CA387777397 | BRCA2 | c.3583C>G (p.Leu1195Val) c.3214C>G (p.Leu1072Val) n.3583C>G | ClinVar dbSNP |
| 13 | g.32337938C>T | CA483437635 | BRCA2 | c.3583C>T (p.Leu1195=) c.3214C>T (p.Leu1072=) n.3583C>T | dbSNP |
| 13 | g.32337939del | CA2580087099 | BRCA2 | c.3584del (p.Leu1195ArgfsTer2) c.3215del (p.Leu1072ArgfsTer2) n.3584del | ClinVar |
| 13 | g.32337939T>A | CA387777399 | BRCA2 | c.3584T>A (p.Leu1195Gln) c.3215T>A (p.Leu1072Gln) n.3584T>A | dbSNP |
| 13 | g.32337939T>C | CA387777404 | BRCA2 | c.3584T>C (p.Leu1195Pro) c.3215T>C (p.Leu1072Pro) n.3584T>C | gnomAD v4 |
| 13 | g.32337939T>G | CA387777402 | BRCA2 | c.3584T>G (p.Leu1195Arg) c.3215T>G (p.Leu1072Arg) n.3584T>G | dbSNP |
| 13 | g.32337940G>A | CA483437636 | BRCA2 | c.3585G>A (p.Leu1195=) c.3216G>A (p.Leu1072=) n.3585G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337940G>C | CA483437637 | BRCA2 | c.3585G>C (p.Leu1195=) c.3216G>C (p.Leu1072=) n.3585G>C | dbSNP gnomAD v4 |
| 13 | g.32337940G>T | CA483437638 | BRCA2 | c.3585G>T (p.Leu1195=) c.3216G>T (p.Leu1072=) n.3585G>T | ClinVar |
| 13 | g.32337941T>A | CA387777406 | BRCA2 | c.3586T>A (p.Leu1196Met) c.3217T>A (p.Leu1073Met) n.3586T>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337941T>C | CA483437640 | BRCA2 | c.3586T>C (p.Leu1196=) c.3217T>C (p.Leu1073=) n.3586T>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32337941T>G | CA387777408 | BRCA2 | c.3586T>G (p.Leu1196Val) c.3217T>G (p.Leu1073Val) n.3586T>G | dbSNP |
| 13 | g.32337941T= | CA2082818573 | BRCA2 | c.3586T= (p.Leu1196=) c.3217T= (p.Leu1073=) n.3586T= | |
| 13 | g.32337942T>A | CA387777410 | BRCA2 | c.3587T>A (p.Leu1196Ter) c.3218T>A (p.Leu1073Ter) n.3587T>A | dbSNP |
| 13 | g.32337942T>C | CA387777412 | BRCA2 | c.3587T>C (p.Leu1196Ser) c.3218T>C (p.Leu1073Ser) n.3587T>C | |
| 13 | g.32337942T>G | CA387777415 | BRCA2 | c.3587T>G (p.Leu1196Trp) c.3218T>G (p.Leu1073Trp) n.3587T>G | |
| 13 | g.32337943G>A | CA6940705 | BRCA2 | c.3588G>A (p.Leu1196=) c.3219G>A (p.Leu1073=) n.3588G>A | ClinVar dbSNP ExAC gnomAD v2 |
| 13 | g.32337943G>C | CA387777417 | BRCA2 | c.3588G>C (p.Leu1196Phe) c.3219G>C (p.Leu1073Phe) n.3588G>C | |
| 13 | g.32337943G= | CA2082818588 | BRCA2 | c.3588G= (p.Leu1196=) c.3219G= (p.Leu1073=) n.3588G= | |
| 13 | g.32337943G>T | CA387777419 | BRCA2 | c.3588G>T (p.Leu1196Phe) c.3219G>T (p.Leu1073Phe) n.3588G>T | |
| 13 | g.32337943_32337944delinsGA | CA2082818581 | BRCA2 | c.3588_3589delinsGA (p.Leu1196=) c.3219_3220delinsGA (p.Leu1073=) n.3588_3589delinsGA | |
| 13 | g.32337944A= | CA2082818601 | BRCA2 | c.3589A= (p.Lys1197=) c.3220A= (p.Lys1074=) n.3589A= | |
| 13 | g.32337944A>C | CA387777422 | BRCA2 | c.3589A>C (p.Lys1197Gln) c.3220A>C (p.Lys1074Gln) n.3589A>C | dbSNP |
| 13 | g.32337944A>G | CA387777425 | BRCA2 | c.3589A>G (p.Lys1197Glu) c.3220A>G (p.Lys1074Glu) n.3589A>G | ClinVar dbSNP |
| 13 | g.32337944A>T | CA387777426 | BRCA2 | c.3589A>T (p.Lys1197Ter) c.3220A>T (p.Lys1074Ter) n.3589A>T | dbSNP |
| 13 | g.32337948dup | CA280072 | BRCA2 | c.3593dup (p.Asn1198LysfsTer2) c.3224dup (p.Asn1075LysfsTer2) n.3593dup | ClinVar dbSNP |
| 13 | g.32337948del | CA018383 | BRCA2 | c.3593del (p.Asn1198MetfsTer11) c.3224del (p.Asn1075MetfsTer11) n.3593del | ClinVar dbSNP |
| 13 | g.32337945A>C | CA387777430 | BRCA2 | c.3590A>C (p.Lys1197Thr) c.3221A>C (p.Lys1074Thr) n.3590A>C | |
| 13 | g.32337945A>G | CA387777432 | BRCA2 | c.3590A>G (p.Lys1197Arg) c.3221A>G (p.Lys1074Arg) n.3590A>G | gnomAD v4 |
| 13 | g.32337945A>T | CA387777433 | BRCA2 | c.3590A>T (p.Lys1197Ile) c.3221A>T (p.Lys1074Ile) n.3590A>T | dbSNP |
| 13 | g.32337946A>C | CA387777436 | BRCA2 | c.3591A>C (p.Lys1197Asn) c.3222A>C (p.Lys1074Asn) n.3591A>C | gnomAD v4 |
| 13 | g.32337946A>G | CA483437645 | BRCA2 | c.3591A>G (p.Lys1197=) c.3222A>G (p.Lys1074=) n.3591A>G | |
| 13 | g.32337946A>T | CA387777439 | BRCA2 | c.3591A>T (p.Lys1197Asn) c.3222A>T (p.Lys1074Asn) n.3591A>T | dbSNP |
| 13 | g.32337947A>C | CA387777442 | BRCA2 | c.3592A>C (p.Asn1198His) c.3223A>C (p.Asn1075His) n.3592A>C | |
| 13 | g.32337947A>G | CA387777443 | BRCA2 | c.3592A>G (p.Asn1198Asp) c.3223A>G (p.Asn1075Asp) n.3592A>G | ClinVar dbSNP |
| 13 | g.32337947A>T | CA387777445 | BRCA2 | c.3592A>T (p.Asn1198Tyr) c.3223A>T (p.Asn1075Tyr) n.3592A>T | |
| 13 | g.32337948A= | CA2082818607 | BRCA2 | c.3593A= (p.Asn1198=) c.3224A= (p.Asn1075=) n.3593A= | |
| 13 | g.32337948A>C | CA387777448 | BRCA2 | c.3593A>C (p.Asn1198Thr) c.3224A>C (p.Asn1075Thr) n.3593A>C | ClinVar dbSNP |
| 13 | g.32337948A>G | CA6940706 | BRCA2 | c.3593A>G (p.Asn1198Ser) c.3224A>G (p.Asn1075Ser) n.3593A>G | ClinVar dbSNP ExAC |
| 13 | g.32337948A>T | CA387777451 | BRCA2 | c.3593A>T (p.Asn1198Ile) c.3224A>T (p.Asn1075Ile) n.3593A>T | dbSNP |
| 13 | g.32337948_32337952delinsATGAC | CA2082818614 | BRCA2 | c.3593_3597delinsATGAC (p.Asn1198=) c.3224_3228delinsATGAC (p.Asn1075=) n.3593_3597delinsATGAC | |
| 13 | g.32337949T>A | CA387777454 | BRCA2 | c.3594T>A (p.Asn1198Lys) c.3225T>A (p.Asn1075Lys) n.3594T>A | dbSNP |
| 13 | g.32337949T>C | CA483437647 | BRCA2 | c.3594T>C (p.Asn1198=) c.3225T>C (p.Asn1075=) n.3594T>C | dbSNP |
| 13 | g.32337949T>G | CA387777455 | BRCA2 | c.3594T>G (p.Asn1198Lys) c.3225T>G (p.Asn1075Lys) n.3594T>G | ClinVar |
| 13 | g.32337951_32337954del | CA10589212 | BRCA2 | c.3596_3599del (p.Asp1199ValfsTer9) c.3227_3230del (p.Asp1076ValfsTer9) n.3596_3599del | ClinVar dbSNP |
| 13 | g.32337950G>A | CA16614292 | BRCA2 | c.3595G>A (p.Asp1199Asn) c.3226G>A (p.Asp1076Asn) n.3595G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337950G>C | CA387777461 | BRCA2 | c.3595G>C (p.Asp1199His) c.3226G>C (p.Asp1076His) n.3595G>C | dbSNP |
| 13 | g.32337950G= | CA2082818631 | BRCA2 | c.3595G= (p.Asp1199=) c.3226G= (p.Asp1076=) n.3595G= | |
| 13 | g.32337950G>T | CA387777459 | BRCA2 | c.3595G>T (p.Asp1199Tyr) c.3226G>T (p.Asp1076Tyr) n.3595G>T | ClinVar dbSNP |
| 13 | g.32337951A>C | CA387777466 | BRCA2 | c.3596A>C (p.Asp1199Ala) c.3227A>C (p.Asp1076Ala) n.3596A>C | |
| 13 | g.32337951A>G | CA387777467 | BRCA2 | c.3596A>G (p.Asp1199Gly) c.3227A>G (p.Asp1076Gly) n.3596A>G | ClinVar dbSNP COSMIC COSMIC |
| 13 | g.32337951A>T | CA387777470 | BRCA2 | c.3596A>T (p.Asp1199Val) c.3227A>T (p.Asp1076Val) n.3596A>T | dbSNP |
| 13 | g.32337952C>A | CA387777472 | BRCA2 | c.3597C>A (p.Asp1199Glu) c.3228C>A (p.Asp1076Glu) n.3597C>A | |
| 13 | g.32337952C= | CA2082818646 | BRCA2 | c.3597C= (p.Asp1199=) c.3228C= (p.Asp1076=) n.3597C= | |
| 13 | g.32337952C>G | CA387777476 | BRCA2 | c.3597C>G (p.Asp1199Glu) c.3228C>G (p.Asp1076Glu) n.3597C>G | ClinVar dbSNP |
| 13 | g.32337952C>T | CA247505390 | BRCA2 | c.3597C>T (p.Asp1199=) c.3228C>T (p.Asp1076=) n.3597C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32337952_32337954delinsCTG | CA2082818643 | BRCA2 | c.3597_3599delinsCTG (p.Asp1199=) c.3228_3230delinsCTG (p.Asp1076=) n.3597_3599delinsCTG | |
| 13 | g.32337953T>A | CA018392 | BRCA2 | c.3598T>A (p.Cys1200Ser) c.3229T>A (p.Cys1077Ser) n.3598T>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337953T>C | CA387777483 | BRCA2 | c.3598T>C (p.Cys1200Arg) c.3229T>C (p.Cys1077Arg) n.3598T>C | |
| 13 | g.32337953T>G | CA247505407 | BRCA2 | c.3598T>G (p.Cys1200Gly) c.3229T>G (p.Cys1077Gly) n.3598T>G | ClinVar dbSNP |
| 13 | g.32337953T= | CA2082818666 | BRCA2 | c.3598T= (p.Cys1200=) c.3229T= (p.Cys1077=) n.3598T= | |
| 13 | g.32337953_32337954delinsTG | CA2082818675 | BRCA2 | c.3598_3599delinsTG (p.Cys1200=) c.3229_3230delinsTG (p.Cys1077=) n.3598_3599delinsTG | |
| 13 | g.32337954_32337955del | CA018389 | BRCA2 | c.3599_3600del (p.Cys1200Ter) c.3230_3231del (p.Cys1077Ter) n.3599_3600del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
| 13 | g.32337954del | CA10586511 | BRCA2 | c.3599del (p.Cys1200LeufsTer9) c.3230del (p.Cys1077LeufsTer9) n.3599del | ClinVar dbSNP |
| 13 | g.32337954G>A | CA387777490 | BRCA2 | c.3599G>A (p.Cys1200Tyr) c.3230G>A (p.Cys1077Tyr) n.3599G>A | ClinVar dbSNP |
| 13 | g.32337954G>C | CA387777491 | BRCA2 | c.3599G>C (p.Cys1200Ser) c.3230G>C (p.Cys1077Ser) n.3599G>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337954G= | CA2082818688 | BRCA2 | c.3599G= (p.Cys1200=) c.3230G= (p.Cys1077=) n.3599G= | |
| 13 | g.32337954G>T | CA387777489 | BRCA2 | c.3599G>T (p.Cys1200Phe) c.3230G>T (p.Cys1077Phe) n.3599G>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32337955del | CA2580087102 | BRCA2 | c.3600del (p.Cys1200Ter) c.3231del (p.Cys1077Ter) n.3600del | ClinVar |
| 13 | g.32337955T>A | CA387777493 | BRCA2 | c.3600T>A (p.Cys1200Ter) c.3231T>A (p.Cys1077Ter) n.3600T>A | ClinVar dbSNP |
| 13 | g.32337955T>C | CA018408 | BRCA2 | c.3600T>C (p.Cys1200=) c.3231T>C (p.Cys1077=) n.3600T>C | ClinVar dbSNP |
| 13 | g.32337955T>G | CA387777494 | BRCA2 | c.3600T>G (p.Cys1200Trp) c.3231T>G (p.Cys1077Trp) n.3600T>G | dbSNP |
| 13 | g.32337955T= | CA2082818706 | BRCA2 | c.3600T= (p.Cys1200=) c.3231T= (p.Cys1077=) n.3600T= | |
| 13 | g.32337955_32337956insTT | CA2499222137 | BRCA2 | c.3600_3601insTT (p.Asn1201LeufsTer9) c.3231_3232insTT (p.Asn1078LeufsTer9) n.3600_3601insTT | |
| 13 | g.32337955dup | CA2573149325 | BRCA2 | c.3600dup (p.Asn1201Ter) c.3231dup (p.Asn1078Ter) n.3600dup | ClinVar dbSNP |
| 13 | g.32337956A= | CA2082818719 | BRCA2 | c.3601A= (p.Asn1201=) c.3232A= (p.Asn1078=) n.3601A= | |
| 13 | g.32337956A>C | CA387777497 | BRCA2 | c.3601A>C (p.Asn1201His) c.3232A>C (p.Asn1078His) n.3601A>C | |
| 13 | g.32337956A>G | CA387777499 | BRCA2 | c.3601A>G (p.Asn1201Asp) c.3232A>G (p.Asn1078Asp) n.3601A>G | ClinVar dbSNP |
| 13 | g.32337956A>T | CA387777500 | BRCA2 | c.3601A>T (p.Asn1201Tyr) c.3232A>T (p.Asn1078Tyr) n.3601A>T | |
| 13 | g.32337956_32337957delinsT | CA2695218188 | BRCA2 | c.3601_3602delinsT (p.Asn1201SerfsTer8) c.3232_3233delinsT (p.Asn1078SerfsTer8) n.3601_3602delinsT | |
| 13 | g.32337957A>C | CA387777503 | BRCA2 | c.3602A>C (p.Asn1201Thr) c.3233A>C (p.Asn1078Thr) n.3602A>C | |
| 13 | g.32337957A>G | CA387777505 | BRCA2 | c.3602A>G (p.Asn1201Ser) c.3233A>G (p.Asn1078Ser) n.3602A>G | dbSNP |
| 13 | g.32337957A>T | CA387777506 | BRCA2 | c.3602A>T (p.Asn1201Ile) c.3233A>T (p.Asn1078Ile) n.3602A>T | dbSNP |
| 13 | g.32337957_32337958delinsAC | CA2082818724 | BRCA2 | c.3602_3603delinsAC (p.Asn1201=) c.3233_3234delinsAC (p.Asn1078=) n.3602_3603delinsAC | |
| 13 | g.32337958del | CA10589213 | BRCA2 | c.3603del (p.Asn1201LysfsTer8) c.3234del (p.Asn1078LysfsTer8) n.3603del | ClinVar dbSNP |
| 13 | g.32337958C>A | CA387777509 | BRCA2 | c.3603C>A (p.Asn1201Lys) c.3234C>A (p.Asn1078Lys) n.3603C>A | |
| 13 | g.32337958C>G | CA387777510 | BRCA2 | c.3603C>G (p.Asn1201Lys) c.3234C>G (p.Asn1078Lys) n.3603C>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32337958C>T | CA483437652 | BRCA2 | c.3603C>T (p.Asn1201=) c.3234C>T (p.Asn1078=) n.3603C>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337959A>C | CA387777514 | BRCA2 | c.3604A>C (p.Lys1202Gln) c.3235A>C (p.Lys1079Gln) n.3604A>C | |
| 13 | g.32337959A>G | CA387777517 | BRCA2 | c.3604A>G (p.Lys1202Glu) c.3235A>G (p.Lys1079Glu) n.3604A>G | ClinVar |
| 13 | g.32337959A>T | CA387777519 | BRCA2 | c.3604A>T (p.Lys1202Ter) c.3235A>T (p.Lys1079Ter) n.3604A>T | dbSNP |
| 13 | g.32337962del | CA2499222139 | BRCA2 | c.3607del (p.Ser1203ValfsTer6) c.3238del (p.Ser1080ValfsTer6) n.3607del | |
| 13 | g.32337961_32337962del | CA2499222138 | BRCA2 | c.3606_3607del (p.Ser1203CysfsTer8) c.3237_3238del (p.Ser1080CysfsTer8) n.3606_3607del | |
| 13 | g.32337960A= | CA2082818733 | BRCA2 | c.3605A= (p.Lys1202=) c.3236A= (p.Lys1079=) n.3605A= | |
| 13 | g.32337960A>C | CA387777522 | BRCA2 | c.3605A>C (p.Lys1202Thr) c.3236A>C (p.Lys1079Thr) n.3605A>C | dbSNP |
| 13 | g.32337960A>G | CA387777520 | BRCA2 | c.3605A>G (p.Lys1202Arg) c.3236A>G (p.Lys1079Arg) n.3605A>G | gnomAD v4 |
| 13 | g.32337960A>T | CA387777521 | BRCA2 | c.3605A>T (p.Lys1202Ile) c.3236A>T (p.Lys1079Ile) n.3605A>T | |
| 13 | g.32337961A>C | CA387777523 | BRCA2 | c.3606A>C (p.Lys1202Asn) c.3237A>C (p.Lys1079Asn) n.3606A>C | |
| 13 | g.32337961A>G | CA483437656 | BRCA2 | c.3606A>G (p.Lys1202=) c.3237A>G (p.Lys1079=) n.3606A>G | |
| 13 | g.32337961A>T | CA387777524 | BRCA2 | c.3606A>T (p.Lys1202Asn) c.3237A>T (p.Lys1079Asn) n.3606A>T | dbSNP |
| 13 | g.32337962A>C | CA387777526 | BRCA2 | c.3607A>C (p.Ser1203Arg) c.3238A>C (p.Ser1080Arg) n.3607A>C | |
| 13 | g.32337962A>G | CA387777528 | BRCA2 | c.3607A>G (p.Ser1203Gly) c.3238A>G (p.Ser1080Gly) n.3607A>G | |
| 13 | g.32337962A>T | CA387777530 | BRCA2 | c.3607A>T (p.Ser1203Cys) c.3238A>T (p.Ser1080Cys) n.3607A>T | dbSNP |
| 13 | g.32337963G>A | CA247505427 | BRCA2 | c.3608G>A (p.Ser1203Asn) c.3239G>A (p.Ser1080Asn) n.3608G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337963G>C | CA247505434 | BRCA2 | c.3608G>C (p.Ser1203Thr) c.3239G>C (p.Ser1080Thr) n.3608G>C | dbSNP |
| 13 | g.32337963G= | CA2082818742 | BRCA2 | c.3608G= (p.Ser1203=) c.3239G= (p.Ser1080=) n.3608G= | |
| 13 | g.32337963G>T | CA6940707 | BRCA2 | c.3608G>T (p.Ser1203Ile) c.3239G>T (p.Ser1080Ile) n.3608G>T | dbSNP ExAC gnomAD v4 |
| 13 | g.32337964T>A | CA387777532 | BRCA2 | c.3609T>A (p.Ser1203Arg) c.3240T>A (p.Ser1080Arg) n.3609T>A | dbSNP |
| 13 | g.32337964T>C | CA483437658 | BRCA2 | c.3609T>C (p.Ser1203=) c.3240T>C (p.Ser1080=) n.3609T>C | dbSNP |
| 13 | g.32337964T>G | CA387777534 | BRCA2 | c.3609T>G (p.Ser1203Arg) c.3240T>G (p.Ser1080Arg) n.3609T>G | ClinVar dbSNP gnomAD v2 |
| 13 | g.32337964T= | CA2082818750 | BRCA2 | c.3609T= (p.Ser1203=) c.3240T= (p.Ser1080=) n.3609T= | |
| 13 | g.32337965G>A | CA387777539 | BRCA2 | c.3610G>A (p.Ala1204Thr) c.3241G>A (p.Ala1081Thr) n.3610G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337965G>C | CA387777538 | BRCA2 | c.3610G>C (p.Ala1204Pro) c.3241G>C (p.Ala1081Pro) n.3610G>C | dbSNP |
| 13 | g.32337965G= | CA2082818760 | BRCA2 | c.3610G= (p.Ala1204=) c.3241G= (p.Ala1081=) n.3610G= | |
| 13 | g.32337965G>T | CA387777536 | BRCA2 | c.3610G>T (p.Ala1204Ser) c.3241G>T (p.Ala1081Ser) n.3610G>T | ClinVar dbSNP |
| 13 | g.32337965_32337968delinsGCTT | CA2082818770 | BRCA2 | c.3610_3613delinsGCTT (p.Ala1204=) c.3241_3244delinsGCTT (p.Ala1081=) n.3610_3613delinsGCTT | |
| 13 | g.32337966C>A | CA387777544 | BRCA2 | c.3611C>A (p.Ala1204Asp) c.3242C>A (p.Ala1081Asp) n.3611C>A | dbSNP |
| 13 | g.32337966C= | CA2082818797 | BRCA2 | c.3611C= (p.Ala1204=) c.3242C= (p.Ala1081=) n.3611C= | |
| 13 | g.32337966C>G | CA387777546 | BRCA2 | c.3611C>G (p.Ala1204Gly) c.3242C>G (p.Ala1081Gly) n.3611C>G | dbSNP |
| 13 | g.32337966C>T | CA387777547 | BRCA2 | c.3611C>T (p.Ala1204Val) c.3242C>T (p.Ala1081Val) n.3611C>T | ClinVar dbSNP |
| 13 | g.32337968_32337970del | CA913188529 | BRCA2 | c.3613_3615del (p.Ser1205del) c.3244_3246del (p.Ser1082del) n.3613_3615del | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32337966_32337967insCAGTAGTCAT | CA2830782341 | BRCA2 | c.3611_3612insCAGTAGTCAT (p.Gly1206SerfsTer9) c.3242_3243insCAGTAGTCAT (p.Gly1083SerfsTer9) n.3611_3612insCAGTAGTCAT | |
| 13 | g.32337967T>A | CA483437659 | BRCA2 | c.3612T>A (p.Ala1204=) c.3243T>A (p.Ala1081=) n.3612T>A | dbSNP |
| 13 | g.32337967T>C | CA338702 | BRCA2 | c.3612T>C (p.Ala1204=) c.3243T>C (p.Ala1081=) n.3612T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337967T>G | CA483437661 | BRCA2 | c.3612T>G (p.Ala1204=) c.3243T>G (p.Ala1081=) n.3612T>G | |
| 13 | g.32337967T= | CA2082818818 | BRCA2 | c.3612T= (p.Ala1204=) c.3243T= (p.Ala1081=) n.3612T= | |
| 13 | g.32337968T>A | CA387777550 | BRCA2 | c.3613T>A (p.Ser1205Thr) c.3244T>A (p.Ser1082Thr) n.3613T>A | dbSNP |
| 13 | g.32337968T>C | CA387777551 | BRCA2 | c.3613T>C (p.Ser1205Pro) c.3244T>C (p.Ser1082Pro) n.3613T>C | |
| 13 | g.32337968T>G | CA387777553 | BRCA2 | c.3613T>G (p.Ser1205Ala) c.3244T>G (p.Ser1082Ala) n.3613T>G | |
| 13 | g.32337969C>A | CA387777556 | BRCA2 | c.3614C>A (p.Ser1205Tyr) c.3245C>A (p.Ser1082Tyr) n.3614C>A | ClinVar |
| 13 | g.32337969C>G | CA387777557 | BRCA2 | c.3614C>G (p.Ser1205Cys) c.3245C>G (p.Ser1082Cys) n.3614C>G | |
| 13 | g.32337969C>T | CA387777559 | BRCA2 | c.3614C>T (p.Ser1205Phe) c.3245C>T (p.Ser1082Phe) n.3614C>T | |
| 13 | g.32337970T>A | CA483437663 | BRCA2 | c.3615T>A (p.Ser1205=) c.3246T>A (p.Ser1082=) n.3615T>A | |
| 13 | g.32337970T>C | CA6940708 | BRCA2 | c.3615T>C (p.Ser1205=) c.3246T>C (p.Ser1082=) n.3615T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32337970T>G | CA483437664 | BRCA2 | c.3615T>G (p.Ser1205=) c.3246T>G (p.Ser1082=) n.3615T>G | |
| 13 | g.32337970T= | CA2082818827 | BRCA2 | c.3615T= (p.Ser1205=) c.3246T= (p.Ser1082=) n.3615T= |