| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32338460_32338496del | CA2825002135 | BRCA2 | c.4105_4141del (p.Ser1369LysfsTer7) c.3736_3772del (p.Ser1246LysfsTer7) n.4105_4141del | ClinVar |
| 13 | g.32338472_32338482delinsT | CA2695199715 | BRCA2 | c.4117_4127delinsT (p.Met1373Ter) c.3748_3758delinsT (p.Met1250Ter) n.4117_4127delinsT | ClinVar |
| 13 | g.32338478_32338479delinsGA | CA2082808474 | BRCA2 | c.4123_4124delinsGA (p.Glu1375=) c.3754_3755delinsGA (p.Glu1252=) n.4123_4124delinsGA | |
| 13 | g.32338480_32338493del | CA2740097654 | BRCA2 | c.4125_4138del (p.Glu1375AspfsTer2) c.3756_3769del (p.Glu1252AspfsTer2) n.4125_4138del | ClinVar |
| 13 | g.32338479del | CA10589242 | BRCA2 | c.4124del (p.Glu1375GlyfsTer13) c.3755del (p.Glu1252GlyfsTer13) n.4124del | ClinVar dbSNP |
| 13 | g.32338479A= | CA2082808483 | BRCA2 | c.4124A= (p.Glu1375=) c.3755A= (p.Glu1252=) n.4124A= | |
| 13 | g.32338479A>C | CA387779343 | BRCA2 | c.4124A>C (p.Glu1375Ala) c.3755A>C (p.Glu1252Ala) n.4124A>C | |
| 13 | g.32338479A>G | CA387779345 | BRCA2 | c.4124A>G (p.Glu1375Gly) c.3755A>G (p.Glu1252Gly) n.4124A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338479A>T | CA387779346 | BRCA2 | c.4124A>T (p.Glu1375Val) c.3755A>T (p.Glu1252Val) n.4124A>T | |
| 13 | g.32338480G>A | CA483438245 | BRCA2 | c.4125G>A (p.Glu1375=) c.3756G>A (p.Glu1252=) n.4125G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338480G>C | CA387779348 | BRCA2 | c.4125G>C (p.Glu1375Asp) c.3756G>C (p.Glu1252Asp) n.4125G>C | dbSNP |
| 13 | g.32338480G= | CA2082808498 | BRCA2 | c.4125G= (p.Glu1375=) c.3756G= (p.Glu1252=) n.4125G= | |
| 13 | g.32338480G>T | CA387779350 | BRCA2 | c.4125G>T (p.Glu1375Asp) c.3756G>T (p.Glu1252Asp) n.4125G>T | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338481G>A | CA387779352 | BRCA2 | c.4126G>A (p.Gly1376Arg) c.3757G>A (p.Gly1253Arg) n.4126G>A | dbSNP COSMIC COSMIC |
| 13 | g.32338481G>C | CA387779354 | BRCA2 | c.4126G>C (p.Gly1376Arg) c.3757G>C (p.Gly1253Arg) n.4126G>C | dbSNP gnomAD v4 |
| 13 | g.32338481G>T | CA387779355 | BRCA2 | c.4126G>T (p.Gly1376Ter) c.3757G>T (p.Gly1253Ter) n.4126G>T | ClinVar dbSNP |
| 13 | g.32338481_32338485delinsGGAAA | CA2082808506 | BRCA2 | c.4126_4130delinsGGAAA (p.Gly1376=) c.3757_3761delinsGGAAA (p.Gly1253=) n.4126_4130delinsGGAAA | |
| 13 | g.32338482G>A | CA387779357 | BRCA2 | c.4127G>A (p.Gly1376Glu) c.3758G>A (p.Gly1253Glu) n.4127G>A | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
| 13 | g.32338482G>C | CA387779359 | BRCA2 | c.4127G>C (p.Gly1376Ala) c.3758G>C (p.Gly1253Ala) n.4127G>C | gnomAD v4 |
| 13 | g.32338482G= | CA2082808527 | BRCA2 | c.4127G= (p.Gly1376=) c.3758G= (p.Gly1253=) n.4127G= | |
| 13 | g.32338482G>T | CA6940752 | BRCA2 | c.4127G>T (p.Gly1376Val) c.3758G>T (p.Gly1253Val) n.4127G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338482_32338483delinsGA | CA2082808531 | BRCA2 | c.4127_4128delinsGA (p.Gly1376=) c.3758_3759delinsGA (p.Gly1253=) n.4127_4128delinsGA | |
| 13 | g.32338482_32338485del | CA019561 | BRCA2 | c.4127_4130del (p.Gly1376AlafsTer11) c.3758_3761del (p.Gly1253AlafsTer11) n.4127_4130del | ClinVar dbSNP |
| 13 | g.32338483A= | CA2082808558 | BRCA2 | c.4128A= (p.Gly1376=) c.3759A= (p.Gly1253=) n.4128A= | |
| 13 | g.32338483A>C | CA483438250 | BRCA2 | c.4128A>C (p.Gly1376=) c.3759A>C (p.Gly1253=) n.4128A>C | |
| 13 | g.32338483A>G | CA483438248 | BRCA2 | c.4128A>G (p.Gly1376=) c.3759A>G (p.Gly1253=) n.4128A>G | |
| 13 | g.32338483A>T | CA483438249 | BRCA2 | c.4128A>T (p.Gly1376=) c.3759A>T (p.Gly1253=) n.4128A>T | ClinVar dbSNP |
| 13 | g.32338485del | CA019568 | BRCA2 | c.4130del (p.Asn1377ThrfsTer11) c.3761del (p.Asn1254ThrfsTer11) n.4130del | ClinVar dbSNP |
| 13 | g.32338484A= | CA2082808567 | BRCA2 | c.4129A= (p.Asn1377=) c.3760A= (p.Asn1254=) n.4129A= | |
| 13 | g.32338484A>C | CA387779362 | BRCA2 | c.4129A>C (p.Asn1377His) c.3760A>C (p.Asn1254His) n.4129A>C | |
| 13 | g.32338484A>G | CA387779364 | BRCA2 | c.4129A>G (p.Asn1377Asp) c.3760A>G (p.Asn1254Asp) n.4129A>G | ClinVar dbSNP |
| 13 | g.32338484A>T | CA387779366 | BRCA2 | c.4129A>T (p.Asn1377Tyr) c.3760A>T (p.Asn1254Tyr) n.4129A>T | dbSNP |
| 13 | g.32338485A= | CA2082808578 | BRCA2 | c.4130A= (p.Asn1377=) c.3761A= (p.Asn1254=) n.4130A= | |
| 13 | g.32338485A>C | CA387779368 | BRCA2 | c.4130A>C (p.Asn1377Thr) c.3761A>C (p.Asn1254Thr) n.4130A>C | |
| 13 | g.32338485A>G | CA6940753 | BRCA2 | c.4130A>G (p.Asn1377Ser) c.3761A>G (p.Asn1254Ser) n.4130A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338485A>T | CA387779372 | BRCA2 | c.4130A>T (p.Asn1377Ile) c.3761A>T (p.Asn1254Ile) n.4130A>T | ClinVar dbSNP |
| 13 | g.32338485_32338486insTGAGGA | CA2695218196 | BRCA2 | c.4130_4131insTGAGGA (p.Asn1377_Thr1378insGluAsp) c.3761_3762insTGAGGA (p.Asn1254_Thr1255insGluAsp) n.4130_4131insTGAGGA | |
| 13 | g.32338487_32338488del | CA2695218195 | BRCA2 | c.4132_4133del (p.Thr1378SerfsTer3) c.3763_3764del (p.Thr1255SerfsTer3) n.4132_4133del | |
| 13 | g.32338485_32338489delinsACACT | CA2082808575 | BRCA2 | c.4130_4134delinsACACT (p.Asn1377=) c.3761_3765delinsACACT (p.Asn1254=) n.4130_4134delinsACACT | |
| 13 | g.32338486C>A | CA387779373 | BRCA2 | c.4131C>A (p.Asn1377Lys) c.3762C>A (p.Asn1254Lys) n.4131C>A | dbSNP |
| 13 | g.32338486C= | CA2082808607 | BRCA2 | c.4131C= (p.Asn1377=) c.3762C= (p.Asn1254=) n.4131C= | |
| 13 | g.32338486C>G | CA387779375 | BRCA2 | c.4131C>G (p.Asn1377Lys) c.3762C>G (p.Asn1254Lys) n.4131C>G | dbSNP |
| 13 | g.32338486C>T | CA483438253 | BRCA2 | c.4131C>T (p.Asn1377=) c.3762C>T (p.Asn1254=) n.4131C>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338488_32338491del | CA019576 | BRCA2 | c.4133_4136del (p.Thr1378ArgfsTer9) c.3764_3767del (p.Thr1255ArgfsTer9) n.4133_4136del | ClinVar dbSNP |
| 13 | g.32338486_32338487insTGAGGA | CA019572 | BRCA2 | c.4131_4132insTGAGGA c.3762_3763insTGAGGA n.4131_4132insTGAGGA | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338487del | CA2573149368 | BRCA2 | c.4132del (p.Thr1378LeufsTer10) c.3763del (p.Thr1255LeufsTer10) n.4132del | ClinVar dbSNP |
| 13 | g.32338487A= | CA2082808618 | BRCA2 | c.4132A= (p.Thr1378=) c.3763A= (p.Thr1255=) n.4132A= | |
| 13 | g.32338487A>C | CA387779377 | BRCA2 | c.4132A>C (p.Thr1378Pro) c.3763A>C (p.Thr1255Pro) n.4132A>C | |
| 13 | g.32338487A>G | CA387779380 | BRCA2 | c.4132A>G (p.Thr1378Ala) c.3763A>G (p.Thr1255Ala) n.4132A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338487A>T | CA387779379 | BRCA2 | c.4132A>T (p.Thr1378Ser) c.3763A>T (p.Thr1255Ser) n.4132A>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338487dup | CA2695218197 | BRCA2 | c.4132dup (p.Thr1378AsnfsTer4) c.3763dup (p.Thr1255AsnfsTer4) n.4132dup | |
| 13 | g.32338488C>A | CA247506544 | BRCA2 | c.4133C>A (p.Thr1378Asn) c.3764C>A (p.Thr1255Asn) n.4133C>A | ClinVar dbSNP |
| 13 | g.32338488C= | CA2082808647 | BRCA2 | c.4133C= (p.Thr1378=) c.3764C= (p.Thr1255=) n.4133C= | |
| 13 | g.32338488C>G | CA387779382 | BRCA2 | c.4133C>G (p.Thr1378Ser) c.3764C>G (p.Thr1255Ser) n.4133C>G | dbSNP |
| 13 | g.32338488C>T | CA387779384 | BRCA2 | c.4133C>T (p.Thr1378Ile) c.3764C>T (p.Thr1255Ile) n.4133C>T | ClinVar dbSNP |
| 13 | g.32338489_32338490del | CA2697551726 | BRCA2 | c.4134_4135del (p.Gln1379AspfsTer2) c.3765_3766del (p.Gln1256AspfsTer2) n.4134_4135del | ClinVar |
| 13 | g.32338489T>A | CA483438255 | BRCA2 | c.4134T>A (p.Thr1378=) c.3765T>A (p.Thr1255=) n.4134T>A | dbSNP |
| 13 | g.32338489T>C | CA483438256 | BRCA2 | c.4134T>C (p.Thr1378=) c.3765T>C (p.Thr1255=) n.4134T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338489T>G | CA483438257 | BRCA2 | c.4134T>G (p.Thr1378=) c.3765T>G (p.Thr1255=) n.4134T>G | ClinVar dbSNP |
| 13 | g.32338489T= | CA2082808654 | BRCA2 | c.4134T= (p.Thr1378=) c.3765T= (p.Thr1255=) n.4134T= | |
| 13 | g.32338489_32338490delinsTC | CA2082808658 | BRCA2 | c.4134_4135delinsTC (p.Thr1378=) c.3765_3766delinsTC (p.Thr1255=) n.4134_4135delinsTC | |
| 13 | g.32338490del | CA658653662 | BRCA2 | c.4135del (p.Gln1379ArgfsTer9) c.3766del (p.Gln1256ArgfsTer9) n.4135del | ClinVar dbSNP |
| 13 | g.32338490C>A | CA387779387 | BRCA2 | c.4135C>A (p.Gln1379Lys) c.3766C>A (p.Gln1256Lys) n.4135C>A | ClinVar dbSNP |
| 13 | g.32338490C= | CA2082808685 | BRCA2 | c.4135C= (p.Gln1379=) c.3766C= (p.Gln1256=) n.4135C= | |
| 13 | g.32338490C>G | CA387779390 | BRCA2 | c.4135C>G (p.Gln1379Glu) c.3766C>G (p.Gln1256Glu) n.4135C>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338490C>T | CA387779388 | BRCA2 | c.4135C>T (p.Gln1379Ter) c.3766C>T (p.Gln1256Ter) n.4135C>T | ClinVar dbSNP |
| 13 | g.32338490_32338495delinsCAGATT | CA2082808682 | BRCA2 | c.4135_4140delinsCAGATT (p.Gln1379=) c.3766_3771delinsCAGATT (p.Gln1256=) n.4135_4140delinsCAGATT | |
| 13 | g.32338491A>C | CA387779392 | BRCA2 | c.4136A>C (p.Gln1379Pro) c.3767A>C (p.Gln1256Pro) n.4136A>C | |
| 13 | g.32338491A>G | CA387779394 | BRCA2 | c.4136A>G (p.Gln1379Arg) c.3767A>G (p.Gln1256Arg) n.4136A>G | dbSNP gnomAD v4 COSMIC |
| 13 | g.32338491A>T | CA387779396 | BRCA2 | c.4136A>T (p.Gln1379Leu) c.3767A>T (p.Gln1256Leu) n.4136A>T | dbSNP |
| 13 | g.32338491dup | CA019581 | BRCA2 | c.4136dup (p.Ile1380AspfsTer2) c.3767dup (p.Ile1257AspfsTer2) n.4136dup | ClinVar dbSNP |
| 13 | g.32338492_32338496del | CA019585 | BRCA2 | c.4137_4141del (p.Ile1380ArgfsTer21) c.3768_3772del (p.Ile1257ArgfsTer21) n.4137_4141del | ClinVar dbSNP |
| 13 | g.32338492G>A | CA6940754 | BRCA2 | c.4137G>A (p.Gln1379=) c.3768G>A (p.Gln1256=) n.4137G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338492G>C | CA387779398 | BRCA2 | c.4137G>C (p.Gln1379His) c.3768G>C (p.Gln1256His) n.4137G>C | ClinVar dbSNP |
| 13 | g.32338492G= | CA2082808698 | BRCA2 | c.4137G= (p.Gln1379=) c.3768G= (p.Gln1256=) n.4137G= | |
| 13 | g.32338492G>T | CA387779399 | BRCA2 | c.4137G>T (p.Gln1379His) c.3768G>T (p.Gln1256His) n.4137G>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338493A= | CA2082808710 | BRCA2 | c.4138A= (p.Ile1380=) c.3769A= (p.Ile1257=) n.4138A= | |
| 13 | g.32338493A>C | CA387779400 | BRCA2 | c.4138A>C (p.Ile1380Leu) c.3769A>C (p.Ile1257Leu) n.4138A>C | |
| 13 | g.32338493A>G | CA387779402 | BRCA2 | c.4138A>G (p.Ile1380Val) c.3769A>G (p.Ile1257Val) n.4138A>G | ClinVar dbSNP |
| 13 | g.32338493A>T | CA387779404 | BRCA2 | c.4138A>T (p.Ile1380Phe) c.3769A>T (p.Ile1257Phe) n.4138A>T | dbSNP |
| 13 | g.32338494T>A | CA387779410 | BRCA2 | c.4139T>A (p.Ile1380Asn) c.3770T>A (p.Ile1257Asn) n.4139T>A | dbSNP |
| 13 | g.32338494T>C | CA387779411 | BRCA2 | c.4139T>C (p.Ile1380Thr) c.3770T>C (p.Ile1257Thr) n.4139T>C | ClinVar dbSNP |
| 13 | g.32338494T>G | CA387779408 | BRCA2 | c.4139T>G (p.Ile1380Ser) c.3770T>G (p.Ile1257Ser) n.4139T>G | |
| 13 | g.32338494_32338495dup | CA019589 | BRCA2 | c.4139_4140dup (p.Lys1381LeufsTer8) c.3770_3771dup (p.Lys1258LeufsTer8) n.4139_4140dup | ClinVar dbSNP |
| 13 | g.32338495T>A | CA483438259 | BRCA2 | c.4140T>A (p.Ile1380=) c.3771T>A (p.Ile1257=) n.4140T>A | |
| 13 | g.32338495T>C | CA483438260 | BRCA2 | c.4140T>C (p.Ile1380=) c.3771T>C (p.Ile1257=) n.4140T>C | |
| 13 | g.32338495T>G | CA019602 | BRCA2 | c.4140T>G (p.Ile1380Met) c.3771T>G (p.Ile1257Met) n.4140T>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338495T= | CA2082808739 | BRCA2 | c.4140T= (p.Ile1380=) c.3771T= (p.Ile1257=) n.4140T= | |
| 13 | g.32338495_32338498delinsTAAA | CA2082808729 | BRCA2 | c.4140_4143delinsTAAA (p.Ile1380=) c.3771_3774delinsTAAA (p.Ile1257=) n.4140_4143delinsTAAA | |
| 13 | g.32338496A>C | CA387779413 | BRCA2 | c.4141A>C (p.Lys1381Gln) c.3772A>C (p.Lys1258Gln) n.4141A>C | |
| 13 | g.32338496A>G | CA387779415 | BRCA2 | c.4141A>G (p.Lys1381Glu) c.3772A>G (p.Lys1258Glu) n.4141A>G | ClinVar gnomAD v4 |
| 13 | g.32338496A>T | CA387779416 | BRCA2 | c.4141A>T (p.Lys1381Ter) c.3772A>T (p.Lys1258Ter) n.4141A>T | dbSNP |
| 13 | g.32338496_32338498del | CA019606 | BRCA2 | c.4141_4143del (p.Lys1381del) c.3772_3774del (p.Lys1258del) n.4141_4143del | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338496_32338499delinsAAAG | CA2082808748 | BRCA2 | c.4141_4144delinsAAAG (p.Lys1381=) c.3772_3775delinsAAAG (p.Lys1258=) n.4141_4144delinsAAAG | |
| 13 | g.32338497A= | CA2082808754 | BRCA2 | c.4142A= (p.Lys1381=) c.3773A= (p.Lys1258=) n.4142A= | |
| 13 | g.32338497A>C | CA387779420 | BRCA2 | c.4142A>C (p.Lys1381Thr) c.3773A>C (p.Lys1258Thr) n.4142A>C | dbSNP |
| 13 | g.32338497A>G | CA387779422 | BRCA2 | c.4142A>G (p.Lys1381Arg) c.3773A>G (p.Lys1258Arg) n.4142A>G | ClinVar dbSNP |
| 13 | g.32338497A>T | CA387779424 | BRCA2 | c.4142A>T (p.Lys1381Ile) c.3773A>T (p.Lys1258Ile) n.4142A>T | dbSNP |
| 13 | g.32338501_32338503del | CA019610 | BRCA2 | c.4146_4148del (p.Glu1382del) c.3777_3779del (p.Glu1259del) n.4146_4148del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338498A>C | CA387779427 | BRCA2 | c.4143A>C (p.Lys1381Asn) c.3774A>C (p.Lys1258Asn) n.4143A>C | |
| 13 | g.32338498A>G | CA483438264 | BRCA2 | c.4143A>G (p.Lys1381=) c.3774A>G (p.Lys1258=) n.4143A>G | ClinVar |
| 13 | g.32338498A>T | CA387779429 | BRCA2 | c.4143A>T (p.Lys1381Asn) c.3774A>T (p.Lys1258Asn) n.4143A>T | dbSNP |
| 13 | g.32338499G>A | CA387779961 | BRCA2 | c.4144G>A (p.Glu1382Lys) c.3775G>A (p.Glu1259Lys) n.4144G>A | dbSNP COSMIC COSMIC |
| 13 | g.32338499G>C | CA387779965 | BRCA2 | c.4144G>C (p.Glu1382Gln) c.3775G>C (p.Glu1259Gln) n.4144G>C | dbSNP |
| 13 | g.32338499G>T | CA387779962 | BRCA2 | c.4144G>T (p.Glu1382Ter) c.3775G>T (p.Glu1259Ter) n.4144G>T | ClinVar |
| 13 | g.32338500A= | CA2082808764 | BRCA2 | c.4145A= (p.Glu1382=) c.3776A= (p.Glu1259=) n.4145A= | |
| 13 | g.32338500A>C | CA387779967 | BRCA2 | c.4145A>C (p.Glu1382Ala) c.3776A>C (p.Glu1259Ala) n.4145A>C | |
| 13 | g.32338500A>G | CA387779969 | BRCA2 | c.4145A>G (p.Glu1382Gly) c.3776A>G (p.Glu1259Gly) n.4145A>G | ClinVar dbSNP |
| 13 | g.32338500A>T | CA387779971 | BRCA2 | c.4145A>T (p.Glu1382Val) c.3776A>T (p.Glu1259Val) n.4145A>T | dbSNP |
| 13 | g.32338500_32338504delinsAAGAT | CA2082808763 | BRCA2 | c.4145_4149delinsAAGAT (p.Glu1382=) c.3776_3780delinsAAGAT (p.Glu1259=) n.4145_4149delinsAAGAT | |
| 13 | g.32338501A= | CA2082808786 | BRCA2 | c.4146A= (p.Glu1382=) c.3777A= (p.Glu1259=) n.4146A= | |
| 13 | g.32338501A>C | CA387779973 | BRCA2 | c.4146A>C (p.Glu1382Asp) c.3777A>C (p.Glu1259Asp) n.4146A>C | COSMIC COSMIC |
| 13 | g.32338501A>G | CA483437815 | BRCA2 | c.4146A>G (p.Glu1382=) c.3777A>G (p.Glu1259=) n.4146A>G | ClinVar gnomAD v4 |
| 13 | g.32338501A>T | CA387779975 | BRCA2 | c.4146A>T (p.Glu1382Asp) c.3777A>T (p.Glu1259Asp) n.4146A>T | dbSNP |
| 13 | g.32338501_32338504del | CA10589243 | BRCA2 | c.4146_4149del (p.Glu1382AspfsTer5) c.3777_3780del (p.Glu1259AspfsTer5) n.4146_4149del | ClinVar dbSNP |
| 13 | g.32338502G>A | CA019617 | BRCA2 | c.4147G>A (p.Asp1383Asn) c.3778G>A (p.Asp1260Asn) n.4147G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338502G>C | CA387779979 | BRCA2 | c.4147G>C (p.Asp1383His) c.3778G>C (p.Asp1260His) n.4147G>C | dbSNP |
| 13 | g.32338502G= | CA2082808805 | BRCA2 | c.4147G= (p.Asp1383=) c.3778G= (p.Asp1260=) n.4147G= | |
| 13 | g.32338502G>T | CA387779981 | BRCA2 | c.4147G>T (p.Asp1383Tyr) c.3778G>T (p.Asp1260Tyr) n.4147G>T | ClinVar dbSNP |
| 13 | g.32338502_32338504delinsGAT | CA2082808807 | BRCA2 | c.4147_4149delinsGAT (p.Asp1383=) c.3778_3780delinsGAT (p.Asp1260=) n.4147_4149delinsGAT | |
| 13 | g.32338503A>C | CA387779986 | BRCA2 | c.4148A>C (p.Asp1383Ala) c.3779A>C (p.Asp1260Ala) n.4148A>C | dbSNP |
| 13 | g.32338503A>G | CA387779988 | BRCA2 | c.4148A>G (p.Asp1383Gly) c.3779A>G (p.Asp1260Gly) n.4148A>G | dbSNP |
| 13 | g.32338503A>T | CA387779985 | BRCA2 | c.4148A>T (p.Asp1383Val) c.3779A>T (p.Asp1260Val) n.4148A>T | ClinVar dbSNP |
| 13 | g.32338503_32338504del | CA10575919 | BRCA2 | c.4148_4149del (p.Asp1383ValfsTer19) c.3779_3780del (p.Asp1260ValfsTer19) n.4148_4149del | ClinVar dbSNP |
| 13 | g.32338503_32338504delinsAT | CA2082808821 | BRCA2 | c.4148_4149delinsAT (p.Asp1383=) c.3779_3780delinsAT (p.Asp1260=) n.4148_4149delinsAT | |
| 13 | g.32338504T>A | CA387779990 | BRCA2 | c.4149T>A (p.Asp1383Glu) c.3780T>A (p.Asp1260Glu) n.4149T>A | dbSNP |
| 13 | g.32338504T>C | CA483437820 | BRCA2 | c.4149T>C (p.Asp1383=) c.3780T>C (p.Asp1260=) n.4149T>C | |
| 13 | g.32338504T>G | CA387779992 | BRCA2 | c.4149T>G (p.Asp1383Glu) c.3780T>G (p.Asp1260Glu) n.4149T>G | dbSNP |
| 13 | g.32338506dup | CA2825002138 | BRCA2 | c.4151dup (p.Leu1384PhefsTer19) c.3782dup (p.Leu1261PhefsTer19) n.4151dup | ClinVar |
| 13 | g.32338506del | CA019620 | BRCA2 | c.4151del (p.Leu1384CysfsTer4) c.3782del (p.Leu1261CysfsTer4) n.4151del | ClinVar dbSNP |
| 13 | g.32338505T>A | CA6940755 | BRCA2 | c.4150T>A (p.Leu1384Met) c.3781T>A (p.Leu1261Met) n.4150T>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338505T>C | CA483437822 | BRCA2 | c.4150T>C (p.Leu1384=) c.3781T>C (p.Leu1261=) n.4150T>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338505T>G | CA387779994 | BRCA2 | c.4150T>G (p.Leu1384Val) c.3781T>G (p.Leu1261Val) n.4150T>G | ClinVar dbSNP |
| 13 | g.32338505T= | CA2082808841 | BRCA2 | c.4150T= (p.Leu1384=) c.3781T= (p.Leu1261=) n.4150T= | |
| 13 | g.32338506T>A | CA019626 | BRCA2 | c.4151T>A (p.Leu1384Ter) c.3782T>A (p.Leu1261Ter) n.4151T>A | ClinVar dbSNP |
| 13 | g.32338506T>C | CA387779996 | BRCA2 | c.4151T>C (p.Leu1384Ser) c.3782T>C (p.Leu1261Ser) n.4151T>C | ClinVar gnomAD v4 |
| 13 | g.32338506T>G | CA387779998 | BRCA2 | c.4151T>G (p.Leu1384Trp) c.3782T>G (p.Leu1261Trp) n.4151T>G | |
| 13 | g.32338506T= | CA2082808870 | BRCA2 | c.4151T= (p.Leu1384=) c.3782T= (p.Leu1261=) n.4151T= | |
| 13 | g.32338507G>A | CA019628 | BRCA2 | c.4152G>A (p.Leu1384=) c.3783G>A (p.Leu1261=) n.4152G>A | ClinVar dbSNP |
| 13 | g.32338507G>C | CA387780001 | BRCA2 | c.4152G>C (p.Leu1384Phe) c.3783G>C (p.Leu1261Phe) n.4152G>C | ClinVar dbSNP |
| 13 | g.32338507G= | CA2082808875 | BRCA2 | c.4152G= (p.Leu1384=) c.3783G= (p.Leu1261=) n.4152G= | |
| 13 | g.32338507G>T | CA387780003 | BRCA2 | c.4152G>T (p.Leu1384Phe) c.3783G>T (p.Leu1261Phe) n.4152G>T | |
| 13 | g.32338508T>A | CA387780006 | BRCA2 | c.4153T>A (p.Ser1385Thr) c.3784T>A (p.Ser1262Thr) n.4153T>A | dbSNP |
| 13 | g.32338508T>C | CA387780009 | BRCA2 | c.4153T>C (p.Ser1385Pro) c.3784T>C (p.Ser1262Pro) n.4153T>C | dbSNP |
| 13 | g.32338508T>G | CA387780005 | BRCA2 | c.4153T>G (p.Ser1385Ala) c.3784T>G (p.Ser1262Ala) n.4153T>G | dbSNP |
| 13 | g.32338509C>A | CA10586520 | BRCA2 | c.4154C>A (p.Ser1385Ter) c.3785C>A (p.Ser1262Ter) n.4154C>A | ClinVar dbSNP |
| 13 | g.32338509C= | CA2082808893 | BRCA2 | c.4154C= (p.Ser1385=) c.3785C= (p.Ser1262=) n.4154C= | |
| 13 | g.32338509C>G | CA387780011 | BRCA2 | c.4154C>G (p.Ser1385Ter) c.3785C>G (p.Ser1262Ter) n.4154C>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338509C>T | CA387780012 | BRCA2 | c.4154C>T (p.Ser1385Leu) c.3785C>T (p.Ser1262Leu) n.4154C>T | dbSNP |
| 13 | g.32338510A= | CA2082808898 | BRCA2 | c.4155A= (p.Ser1385=) c.3786A= (p.Ser1262=) n.4155A= | |
| 13 | g.32338510A>C | CA483437828 | BRCA2 | c.4155A>C (p.Ser1385=) c.3786A>C (p.Ser1262=) n.4155A>C | |
| 13 | g.32338510A>G | CA483437829 | BRCA2 | c.4155A>G (p.Ser1385=) c.3786A>G (p.Ser1262=) n.4155A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338510A>T | CA483437830 | BRCA2 | c.4155A>T (p.Ser1385=) c.3786A>T (p.Ser1262=) n.4155A>T | dbSNP |
| 13 | g.32338511G>A | CA387780015 | BRCA2 | c.4156G>A (p.Asp1386Asn) c.3787G>A (p.Asp1263Asn) n.4156G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338511G>C | CA387780017 | BRCA2 | c.4156G>C (p.Asp1386His) c.3787G>C (p.Asp1263His) n.4156G>C | dbSNP |
| 13 | g.32338511G= | CA2082808915 | BRCA2 | c.4156G= (p.Asp1386=) c.3787G= (p.Asp1263=) n.4156G= | |
| 13 | g.32338511G>T | CA387780018 | BRCA2 | c.4156G>T (p.Asp1386Tyr) c.3787G>T (p.Asp1263Tyr) n.4156G>T | ClinVar dbSNP COSMIC COSMIC |
| 13 | g.32338511_32338512delinsGA | CA2082808949 | BRCA2 | c.4156_4157delinsGA (p.Asp1386=) c.3787_3788delinsGA (p.Asp1263=) n.4156_4157delinsGA | |
| 13 | g.32338511_32338512delinsTG | CA1139663189 | BRCA2 | c.4156_4157delinsTG (p.Asp1386Cys) c.3787_3788delinsTG (p.Asp1263Cys) n.4156_4157delinsTG | ClinVar dbSNP |
| 13 | g.32338512A= | CA2082808967 | BRCA2 | c.4157A= (p.Asp1386=) c.3788A= (p.Asp1263=) n.4157A= | |
| 13 | g.32338512A>C | CA387780021 | BRCA2 | c.4157A>C (p.Asp1386Ala) c.3788A>C (p.Asp1263Ala) n.4157A>C | |
| 13 | g.32338512A>G | CA387780023 | BRCA2 | c.4157A>G (p.Asp1386Gly) c.3788A>G (p.Asp1263Gly) n.4157A>G | ClinVar dbSNP |
| 13 | g.32338512A>T | CA019633 | BRCA2 | c.4157A>T (p.Asp1386Val) c.3788A>T (p.Asp1263Val) n.4157A>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338513T>A | CA387780025 | BRCA2 | c.4158T>A (p.Asp1386Glu) c.3789T>A (p.Asp1263Glu) n.4158T>A | dbSNP |
| 13 | g.32338513T>C | CA483437833 | BRCA2 | c.4158T>C (p.Asp1386=) c.3789T>C (p.Asp1263=) n.4158T>C | dbSNP |
| 13 | g.32338513T>G | CA387780027 | BRCA2 | c.4158T>G (p.Asp1386Glu) c.3789T>G (p.Asp1263Glu) n.4158T>G | dbSNP gnomAD v4 |
| 13 | g.32338514T>A | CA019635 | BRCA2 | c.4159T>A (p.Leu1387Ile) c.3790T>A (p.Leu1264Ile) n.4159T>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338514T>C | CA483437835 | BRCA2 | c.4159T>C (p.Leu1387=) c.3790T>C (p.Leu1264=) n.4159T>C | |
| 13 | g.32338514T>G | CA387780031 | BRCA2 | c.4159T>G (p.Leu1387Val) c.3790T>G (p.Leu1264Val) n.4159T>G | dbSNP |
| 13 | g.32338514T= | CA2082808975 | BRCA2 | c.4159T= (p.Leu1387=) c.3790T= (p.Leu1264=) n.4159T= | |
| 13 | g.32338516_32338520del | CA2499222155 | BRCA2 | c.4161_4165del (p.Leu1387PhefsTer14) c.3792_3796del (p.Leu1264PhefsTer14) n.4161_4165del | |
| 13 | g.32338515T>A | CA387780038 | BRCA2 | c.4160T>A (p.Leu1387Ter) c.3791T>A (p.Leu1264Ter) n.4160T>A | dbSNP |
| 13 | g.32338515T>C | CA387780035 | BRCA2 | c.4160T>C (p.Leu1387Ser) c.3791T>C (p.Leu1264Ser) n.4160T>C | gnomAD v4 |
| 13 | g.32338515T>G | CA387780033 | BRCA2 | c.4160T>G (p.Leu1387Ter) c.3791T>G (p.Leu1264Ter) n.4160T>G | |
| 13 | g.32338515T= | CA2082808981 | BRCA2 | c.4160T= (p.Leu1387=) c.3791T= (p.Leu1264=) n.4160T= | |
| 13 | g.32338515_32338516insGG | CA2082808996 | BRCA2 | c.4160_4161insGG (p.Thr1388GlufsTer23) c.3791_3792insGG (p.Thr1265GlufsTer23) n.4160_4161insGG | dbSNP |
| 13 | g.32338515_32338516insTAA | CA2697551728 | BRCA2 | c.4160_4161insTAA (p.Leu1387delinsPheLys) c.3791_3792insTAA (p.Leu1264delinsPheLys) n.4160_4161insTAA | ClinVar |
| 13 | g.32338515_32338516insGGAAG | CA6940756 | BRCA2 | c.4160_4161insGGAAG (p.Thr1388GlufsTer24) c.3791_3792insGGAAG (p.Thr1265GlufsTer24) n.4160_4161insGGAAG | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338516A= | CA2082809010 | BRCA2 | c.4161A= (p.Leu1387=) c.3792A= (p.Leu1264=) n.4161A= | |
| 13 | g.32338516A>C | CA387780042 | BRCA2 | c.4161A>C (p.Leu1387Phe) c.3792A>C (p.Leu1264Phe) n.4161A>C | |
| 13 | g.32338516A>G | CA483437841 | BRCA2 | c.4161A>G (p.Leu1387=) c.3792A>G (p.Leu1264=) n.4161A>G | dbSNP |
| 13 | g.32338516A>T | CA387780040 | BRCA2 | c.4161A>T (p.Leu1387Phe) c.3792A>T (p.Leu1264Phe) n.4161A>T | dbSNP |
| 13 | g.32338516_32338521delinsAACTTT | CA2082809007 | BRCA2 | c.4161_4166delinsAACTTT (p.Leu1387=) c.3792_3797delinsAACTTT (p.Leu1264=) n.4161_4166delinsAACTTT | |
| 13 | g.32338517A= | CA2082809025 | BRCA2 | c.4162A= (p.Thr1388=) c.3793A= (p.Thr1265=) n.4162A= | |
| 13 | g.32338517A>C | CA387780044 | BRCA2 | c.4162A>C (p.Thr1388Pro) c.3793A>C (p.Thr1265Pro) n.4162A>C | ClinVar dbSNP |
| 13 | g.32338517A>G | CA387780047 | BRCA2 | c.4162A>G (p.Thr1388Ala) c.3793A>G (p.Thr1265Ala) n.4162A>G | |
| 13 | g.32338517A>T | CA387780048 | BRCA2 | c.4162A>T (p.Thr1388Ser) c.3793A>T (p.Thr1265Ser) n.4162A>T | |
| 13 | g.32338517_32338519delinsACT | CA2082809022 | BRCA2 | c.4162_4164delinsACT (p.Thr1388=) c.3793_3795delinsACT (p.Thr1265=) n.4162_4164delinsACT | |
| 13 | g.32338517_32338521del | CA6940757 | BRCA2 | c.4162_4166del (p.Thr1388PhefsTer13) c.3793_3797del (p.Thr1265PhefsTer13) n.4162_4166del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338518del | CA1139768323 | BRCA2 | c.4163del (p.Thr1388IlefsTer22) c.3794del (p.Thr1265IlefsTer22) n.4163del | ClinVar gnomAD v4 |
| 13 | g.32338518C>A | CA019646 | BRCA2 | c.4163C>A (p.Thr1388Asn) c.3794C>A (p.Thr1265Asn) n.4163C>A | ClinVar dbSNP ExAC gnomAD v3 gnomAD v4 |
| 13 | g.32338518C= | CA2082809040 | BRCA2 | c.4163C= (p.Thr1388=) c.3794C= (p.Thr1265=) n.4163C= | |
| 13 | g.32338518C>G | CA387780049 | BRCA2 | c.4163C>G (p.Thr1388Ser) c.3794C>G (p.Thr1265Ser) n.4163C>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338518C>T | CA387780051 | BRCA2 | c.4163C>T (p.Thr1388Ile) c.3794C>T (p.Thr1265Ile) n.4163C>T | |
| 13 | g.32338518_32338519delinsA | CA019640 | BRCA2 | c.4163_4164delinsA (p.Thr1388AsnfsTer22) c.3794_3795delinsA (p.Thr1265AsnfsTer22) n.4163_4164delinsA | ClinVar dbSNP |
| 13 | g.32338518_32338520delinsCTT | CA2082809048 | BRCA2 | c.4163_4165delinsCTT (p.Thr1388=) c.3794_3796delinsCTT (p.Thr1265=) n.4163_4165delinsCTT | |
| 13 | g.32338519T>A | CA247507333 | BRCA2 | c.4164T>A (p.Thr1388=) c.3795T>A (p.Thr1265=) n.4164T>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338519T>C | CA483437850 | BRCA2 | c.4164T>C (p.Thr1388=) c.3795T>C (p.Thr1265=) n.4164T>C | ClinVar dbSNP |
| 13 | g.32338519T>G | CA483437851 | BRCA2 | c.4164T>G (p.Thr1388=) c.3795T>G (p.Thr1265=) n.4164T>G | ClinVar |
| 13 | g.32338519T= | CA2082809073 | BRCA2 | c.4164T= (p.Thr1388=) c.3795T= (p.Thr1265=) n.4164T= | |
| 13 | g.32338524dup | CA10589244 | BRCA2 | c.4169dup (p.Leu1390PhefsTer13) c.3800dup (p.Leu1267PhefsTer13) n.4169dup | ClinVar dbSNP |
| 13 | g.32338524del | CA019655 | BRCA2 | c.4169del (p.Leu1390TrpfsTer20) c.3800del (p.Leu1267TrpfsTer20) n.4169del | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338523_32338524del | CA019652 | BRCA2 | c.4168_4169del (p.Leu1390GlyfsTer12) c.3799_3800del (p.Leu1267GlyfsTer12) n.4168_4169del | ClinVar dbSNP |
| 13 | g.32338521_32338524del | CA2499222156 | BRCA2 | c.4166_4169del (p.Phe1389TrpfsTer20) c.3797_3800del (p.Phe1266TrpfsTer20) n.4166_4169del | |
| 13 | g.32338520T>A | CA387780057 | BRCA2 | c.4165T>A (p.Phe1389Ile) c.3796T>A (p.Phe1266Ile) n.4165T>A | ClinVar dbSNP |
| 13 | g.32338520T>C | CA387780059 | BRCA2 | c.4165T>C (p.Phe1389Leu) c.3796T>C (p.Phe1266Leu) n.4165T>C | ClinVar dbSNP |
| 13 | g.32338520T>G | CA16020672 | BRCA2 | c.4165T>G (p.Phe1389Val) c.3796T>G (p.Phe1266Val) n.4165T>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 13 | g.32338520T= | CA2082809086 | BRCA2 | c.4165T= (p.Phe1389=) c.3796T= (p.Phe1266=) n.4165T= | |
| 13 | g.32338521T>A | CA387780061 | BRCA2 | c.4166T>A (p.Phe1389Tyr) c.3797T>A (p.Phe1266Tyr) n.4166T>A | |
| 13 | g.32338521T>C | CA387780063 | BRCA2 | c.4166T>C (p.Phe1389Ser) c.3797T>C (p.Phe1266Ser) n.4166T>C | ClinVar dbSNP |
| 13 | g.32338521T>G | CA387780064 | BRCA2 | c.4166T>G (p.Phe1389Cys) c.3797T>G (p.Phe1266Cys) n.4166T>G | |
| 13 | g.32338521T= | CA2082809094 | BRCA2 | c.4166T= (p.Phe1389=) c.3797T= (p.Phe1266=) n.4166T= | |
| 13 | g.32338522T>A | CA387780069 | BRCA2 | c.4167T>A (p.Phe1389Leu) c.3798T>A (p.Phe1266Leu) n.4167T>A | |
| 13 | g.32338522T>C | CA483437857 | BRCA2 | c.4167T>C (p.Phe1389=) c.3798T>C (p.Phe1266=) n.4167T>C | ClinVar |
| 13 | g.32338522T>G | CA387780066 | BRCA2 | c.4167T>G (p.Phe1389Leu) c.3798T>G (p.Phe1266Leu) n.4167T>G | |
| 13 | g.32338523T>A | CA387780071 | BRCA2 | c.4168T>A (p.Leu1390Met) c.3799T>A (p.Leu1267Met) n.4168T>A | dbSNP |
| 13 | g.32338523T>C | CA483437861 | BRCA2 | c.4168T>C (p.Leu1390=) c.3799T>C (p.Leu1267=) n.4168T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338523T>G | CA387780070 | BRCA2 | c.4168T>G (p.Leu1390Val) c.3799T>G (p.Leu1267Val) n.4168T>G | |
| 13 | g.32338523T= | CA2082809107 | BRCA2 | c.4168T= (p.Leu1390=) c.3799T= (p.Leu1267=) n.4168T= | |
| 13 | g.32338524T>A | CA387780074 | BRCA2 | c.4169T>A (p.Leu1390Ter) c.3800T>A (p.Leu1267Ter) n.4169T>A | |
| 13 | g.32338524T>C | CA387780075 | BRCA2 | c.4169T>C (p.Leu1390Ser) c.3800T>C (p.Leu1267Ser) n.4169T>C | |
| 13 | g.32338524T>G | CA387780076 | BRCA2 | c.4169T>G (p.Leu1390Trp) c.3800T>G (p.Leu1267Trp) n.4169T>G | ClinVar dbSNP |
| 13 | g.32338524T= | CA2082809126 | BRCA2 | c.4169T= (p.Leu1390=) c.3800T= (p.Leu1267=) n.4169T= | |
| 13 | g.32338524_32338525delinsTG | CA2082809123 | BRCA2 | c.4169_4170delinsTG (p.Leu1390=) c.3800_3801delinsTG (p.Leu1267=) n.4169_4170delinsTG | |
| 13 | g.32338524_32338526delinsTGG | CA2082809124 | BRCA2 | c.4169_4171delinsTGG (p.Leu1390=) c.3800_3802delinsTGG (p.Leu1267=) n.4169_4171delinsTGG | |
| 13 | g.32338525G>A | CA483437865 | BRCA2 | c.4170G>A (p.Leu1390=) c.3801G>A (p.Leu1267=) n.4170G>A | ClinVar dbSNP COSMIC COSMIC |
| 13 | g.32338525G>C | CA387780079 | BRCA2 | c.4170G>C (p.Leu1390Phe) c.3801G>C (p.Leu1267Phe) n.4170G>C | dbSNP |
| 13 | g.32338525G= | CA2082809148 | BRCA2 | c.4170G= (p.Leu1390=) c.3801G= (p.Leu1267=) n.4170G= | |
| 13 | g.32338525G>T | CA387780081 | BRCA2 | c.4170G>T (p.Leu1390Phe) c.3801G>T (p.Leu1267Phe) n.4170G>T | dbSNP |
| 13 | g.32338525_32338526del | CA10583100 | BRCA2 | c.4170_4171del (p.Glu1391SerfsTer11) c.3801_3802del (p.Glu1268SerfsTer11) n.4170_4171del | ClinVar dbSNP |
| 13 | g.32338526dup | CA2580087256 | BRCA2 | c.4171dup (p.Glu1391GlyfsTer12) c.3802dup (p.Glu1268GlyfsTer12) n.4171dup | ClinVar |
| 13 | g.32338526del | CA019663 | BRCA2 | c.4171del (p.Glu1391LysfsTer19) c.3802del (p.Glu1268LysfsTer19) n.4171del | ClinVar dbSNP |
| 13 | g.32338526G>A | CA387780084 | BRCA2 | c.4171G>A (p.Glu1391Lys) c.3802G>A (p.Glu1268Lys) n.4171G>A | ClinVar dbSNP |
| 13 | g.32338526G>C | CA387780086 | BRCA2 | c.4171G>C (p.Glu1391Gln) c.3802G>C (p.Glu1268Gln) n.4171G>C | dbSNP |
| 13 | g.32338526G= | CA2082809157 | BRCA2 | c.4171G= (p.Glu1391=) c.3802G= (p.Glu1268=) n.4171G= | |
| 13 | g.32338526G>T | CA387780083 | BRCA2 | c.4171G>T (p.Glu1391Ter) c.3802G>T (p.Glu1268Ter) n.4171G>T | ClinVar dbSNP |
| 13 | g.32338527A>C | CA387780088 | BRCA2 | c.4172A>C (p.Glu1391Ala) c.3803A>C (p.Glu1268Ala) n.4172A>C | |
| 13 | g.32338527A>G | CA387780089 | BRCA2 | c.4172A>G (p.Glu1391Gly) c.3803A>G (p.Glu1268Gly) n.4172A>G | ClinVar dbSNP |
| 13 | g.32338527A>T | CA387780091 | BRCA2 | c.4172A>T (p.Glu1391Val) c.3803A>T (p.Glu1268Val) n.4172A>T | dbSNP |
| 13 | g.32338527_32338530del | CA2695218198 | BRCA2 | c.4172_4175del (p.Glu1391ValfsTer18) c.3803_3806del (p.Glu1268ValfsTer18) n.4172_4175del | |
| 13 | g.32338528A>C | CA387780093 | BRCA2 | c.4173A>C (p.Glu1391Asp) c.3804A>C (p.Glu1268Asp) n.4173A>C | |
| 13 | g.32338528A>G | CA483437868 | BRCA2 | c.4173A>G (p.Glu1391=) c.3804A>G (p.Glu1268=) n.4173A>G | dbSNP gnomAD v4 |
| 13 | g.32338528A>T | CA387780095 | BRCA2 | c.4173A>T (p.Glu1391Asp) c.3804A>T (p.Glu1268Asp) n.4173A>T | dbSNP |
| 13 | g.32338529G>A | CA019667 | BRCA2 | c.4174G>A (p.Val1392Ile) c.3805G>A (p.Val1269Ile) n.4174G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338529G>C | CA387780098 | BRCA2 | c.4174G>C (p.Val1392Leu) c.3805G>C (p.Val1269Leu) n.4174G>C | dbSNP |
| 13 | g.32338529G= | CA2082809162 | BRCA2 | c.4174G= (p.Val1392=) c.3805G= (p.Val1269=) n.4174G= | |
| 13 | g.32338529G>T | CA387780100 | BRCA2 | c.4174G>T (p.Val1392Phe) c.3805G>T (p.Val1269Phe) n.4174G>T | dbSNP |
| 13 | g.32338529_32338530delinsGT | CA2082809167 | BRCA2 | c.4174_4175delinsGT (p.Val1392=) c.3805_3806delinsGT (p.Val1269=) n.4174_4175delinsGT | |
| 13 | g.32338530T>A | CA387780102 | BRCA2 | c.4175T>A (p.Val1392Asp) c.3806T>A (p.Val1269Asp) n.4175T>A | dbSNP |
| 13 | g.32338530T>C | CA387780104 | BRCA2 | c.4175T>C (p.Val1392Ala) c.3806T>C (p.Val1269Ala) n.4175T>C | dbSNP |
| 13 | g.32338530T>G | CA387780106 | BRCA2 | c.4175T>G (p.Val1392Gly) c.3806T>G (p.Val1269Gly) n.4175T>G | dbSNP |
| 13 | g.32338531del | CA335700 | BRCA2 | c.4176del (p.Ala1393ArgfsTer17) c.3807del (p.Ala1270ArgfsTer17) n.4176del | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338531T>A | CA483437876 | BRCA2 | c.4176T>A (p.Val1392=) c.3807T>A (p.Val1269=) n.4176T>A | dbSNP |
| 13 | g.32338531T>C | CA483437877 | BRCA2 | c.4176T>C (p.Val1392=) c.3807T>C (p.Val1269=) n.4176T>C | |
| 13 | g.32338531T>G | CA483437878 | BRCA2 | c.4176T>G (p.Val1392=) c.3807T>G (p.Val1269=) n.4176T>G | |
| 13 | g.32338531T= | CA2082809178 | BRCA2 | c.4176T= (p.Val1392=) c.3807T= (p.Val1269=) n.4176T= | |
| 13 | g.32338532G>A | CA387780112 | BRCA2 | c.4177G>A (p.Ala1393Thr) c.3808G>A (p.Ala1270Thr) n.4177G>A | dbSNP |
| 13 | g.32338532G>C | CA387780109 | BRCA2 | c.4177G>C (p.Ala1393Pro) c.3808G>C (p.Ala1270Pro) n.4177G>C | dbSNP |
| 13 | g.32338532G>T | CA387780111 | BRCA2 | c.4177G>T (p.Ala1393Ser) c.3808G>T (p.Ala1270Ser) n.4177G>T | dbSNP |
| 13 | g.32338532dup | CA10579602 | BRCA2 | c.4177dup (p.Ala1393GlyfsTer10) c.3808dup (p.Ala1270GlyfsTer10) n.4177dup | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338533C>A | CA387780113 | BRCA2 | c.4178C>A (p.Ala1393Glu) c.3809C>A (p.Ala1270Glu) n.4178C>A | dbSNP |
| 13 | g.32338533C= | CA2082809188 | BRCA2 | c.4178C= (p.Ala1393=) c.3809C= (p.Ala1270=) n.4178C= | |
| 13 | g.32338533C>G | CA019671 | BRCA2 | c.4178C>G (p.Ala1393Gly) c.3809C>G (p.Ala1270Gly) n.4178C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338533C>T | CA019676 | BRCA2 | c.4178C>T (p.Ala1393Val) c.3809C>T (p.Ala1270Val) n.4178C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 13 | g.32338534G>A | CA019680 | BRCA2 | c.4179G>A (p.Ala1393=) c.3810G>A (p.Ala1270=) n.4179G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 13 | g.32338534G>C | CA483437882 | BRCA2 | c.4179G>C (p.Ala1393=) c.3810G>C (p.Ala1270=) n.4179G>C | ClinVar dbSNP |
| 13 | g.32338534G= | CA2082809208 | BRCA2 | c.4179G= (p.Ala1393=) c.3810G= (p.Ala1270=) n.4179G= | |
| 13 | g.32338534G>T | CA483437883 | BRCA2 | c.4179G>T (p.Ala1393=) c.3810G>T (p.Ala1270=) n.4179G>T | dbSNP |
| 13 | g.32338535A>C | CA387780117 | BRCA2 | c.4180A>C (p.Lys1394Gln) c.3811A>C (p.Lys1271Gln) n.4180A>C | |
| 13 | g.32338535A>G | CA387780118 | BRCA2 | c.4180A>G (p.Lys1394Glu) c.3811A>G (p.Lys1271Glu) n.4180A>G | |
| 13 | g.32338535A>T | CA387780120 | BRCA2 | c.4180A>T (p.Lys1394Ter) c.3811A>T (p.Lys1271Ter) n.4180A>T | dbSNP |
| 13 | g.32338536A>C | CA387780122 | BRCA2 | c.4181A>C (p.Lys1394Thr) c.3812A>C (p.Lys1271Thr) n.4181A>C | |
| 13 | g.32338536A>G | CA387780124 | BRCA2 | c.4181A>G (p.Lys1394Arg) c.3812A>G (p.Lys1271Arg) n.4181A>G | dbSNP |
| 13 | g.32338536A>T | CA387780126 | BRCA2 | c.4181A>T (p.Lys1394Ile) c.3812A>T (p.Lys1271Ile) n.4181A>T | dbSNP |
| 13 | g.32338537A>C | CA387780128 | BRCA2 | c.4182A>C (p.Lys1394Asn) c.3813A>C (p.Lys1271Asn) n.4182A>C | |
| 13 | g.32338537A>G | CA483437886 | BRCA2 | c.4182A>G (p.Lys1394=) c.3813A>G (p.Lys1271=) n.4182A>G | ClinVar dbSNP |
| 13 | g.32338537A>T | CA387780130 | BRCA2 | c.4182A>T (p.Lys1394Asn) c.3813A>T (p.Lys1271Asn) n.4182A>T | dbSNP |
| 13 | g.32338537_32338538delinsAG | CA2082809211 | BRCA2 | c.4182_4183delinsAG (p.Lys1394=) c.3813_3814delinsAG (p.Lys1271=) n.4182_4183delinsAG | |
| 13 | g.32338538del | CA1139663190 | BRCA2 | c.4183del (p.Ala1395LeufsTer15) c.3814del (p.Ala1272LeufsTer15) n.4183del | ClinVar dbSNP |
| 13 | g.32338538G>A | CA387780133 | BRCA2 | c.4183G>A (p.Ala1395Thr) c.3814G>A (p.Ala1272Thr) n.4183G>A | dbSNP |
| 13 | g.32338538G>C | CA387780135 | BRCA2 | c.4183G>C (p.Ala1395Pro) c.3814G>C (p.Ala1272Pro) n.4183G>C | dbSNP |
| 13 | g.32338538G= | CA2082809217 | BRCA2 | c.4183G= (p.Ala1395=) c.3814G= (p.Ala1272=) n.4183G= | |
| 13 | g.32338538G>T | CA019684 | BRCA2 | c.4183G>T (p.Ala1395Ser) c.3814G>T (p.Ala1272Ser) n.4183G>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338539C>A | CA387780141 | BRCA2 | c.4184C>A (p.Ala1395Asp) c.3815C>A (p.Ala1272Asp) n.4184C>A | dbSNP |
| 13 | g.32338539C= | CA2082809231 | BRCA2 | c.4184C= (p.Ala1395=) c.3815C= (p.Ala1272=) n.4184C= | |
| 13 | g.32338539C>G | CA387780137 | BRCA2 | c.4184C>G (p.Ala1395Gly) c.3815C>G (p.Ala1272Gly) n.4184C>G | dbSNP |
| 13 | g.32338539C>T | CA387780139 | BRCA2 | c.4184C>T (p.Ala1395Val) c.3815C>T (p.Ala1272Val) n.4184C>T | ClinVar dbSNP |
| 13 | g.32338539dup | CA2573053809 | BRCA2 | c.4184dup (p.Gln1396SerfsTer7) c.3815dup (p.Gln1273SerfsTer7) n.4184dup | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338540T>A | CA483437891 | BRCA2 | c.4185T>A (p.Ala1395=) c.3816T>A (p.Ala1272=) n.4185T>A | dbSNP |
| 13 | g.32338540T>C | CA483437892 | BRCA2 | c.4185T>C (p.Ala1395=) c.3816T>C (p.Ala1272=) n.4185T>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338540T>G | CA483437894 | BRCA2 | c.4185T>G (p.Ala1395=) c.3816T>G (p.Ala1272=) n.4185T>G | ClinVar dbSNP |
| 13 | g.32338540T= | CA2082809236 | BRCA2 | c.4185T= (p.Ala1395=) c.3816T= (p.Ala1272=) n.4185T= | |
| 13 | g.32338540_32338576del | CA2580087257 | BRCA2 | c.4185_4221del (p.Gln1396SerfsTer2) c.3816_3852del (p.Gln1273SerfsTer2) n.4185_4221del | ClinVar |
| 13 | g.32338541C>A | CA387780143 | BRCA2 | c.4186C>A (p.Gln1396Lys) c.3817C>A (p.Gln1273Lys) n.4186C>A | ClinVar dbSNP |
| 13 | g.32338541C= | CA2082809241 | BRCA2 | c.4186C= (p.Gln1396=) c.3817C= (p.Gln1273=) n.4186C= | |
| 13 | g.32338541C>G | CA6940758 | BRCA2 | c.4186C>G (p.Gln1396Glu) c.3817C>G (p.Gln1273Glu) n.4186C>G | dbSNP ExAC |
| 13 | g.32338541C>T | CA387780145 | BRCA2 | c.4186C>T (p.Gln1396Ter) c.3817C>T (p.Gln1273Ter) n.4186C>T | ClinVar dbSNP |
| 13 | g.32338541_32338542delinsCA | CA2082809240 | BRCA2 | c.4186_4187delinsCA (p.Gln1396=) c.3817_3818delinsCA (p.Gln1273=) n.4186_4187delinsCA | |
| 13 | g.32338542A= | CA2082809249 | BRCA2 | c.4187A= (p.Gln1396=) c.3818A= (p.Gln1273=) n.4187A= | |
| 13 | g.32338542A>C | CA387780151 | BRCA2 | c.4187A>C (p.Gln1396Pro) c.3818A>C (p.Gln1273Pro) n.4187A>C | |
| 13 | g.32338542A>G | CA019687 | BRCA2 | c.4187A>G (p.Gln1396Arg) c.3818A>G (p.Gln1273Arg) n.4187A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338542A>T | CA387780149 | BRCA2 | c.4187A>T (p.Gln1396Leu) c.3818A>T (p.Gln1273Leu) n.4187A>T | dbSNP gnomAD v4 |
| 13 | g.32338543del | CA019693 | BRCA2 | c.4188del (p.Glu1397LysfsTer13) c.3819del (p.Glu1274LysfsTer13) n.4188del | ClinVar dbSNP |
| 13 | g.32338543A= | CA2082809256 | BRCA2 | c.4188A= (p.Gln1396=) c.3819A= (p.Gln1273=) n.4188A= | |
| 13 | g.32338543A>C | CA387780153 | BRCA2 | c.4188A>C (p.Gln1396His) c.3819A>C (p.Gln1273His) n.4188A>C | |
| 13 | g.32338543A>G | CA483437899 | BRCA2 | c.4188A>G (p.Gln1396=) c.3819A>G (p.Gln1273=) n.4188A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338543A>T | CA387780156 | BRCA2 | c.4188A>T (p.Gln1396His) c.3819A>T (p.Gln1273His) n.4188A>T | |
| 13 | g.32338544G>A | CA019698 | BRCA2 | c.4189G>A (p.Glu1397Lys) c.3820G>A (p.Glu1274Lys) n.4189G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338544G>C | CA387780160 | BRCA2 | c.4189G>C (p.Glu1397Gln) c.3820G>C (p.Glu1274Gln) n.4189G>C | ClinVar dbSNP |
| 13 | g.32338544G= | CA2082809262 | BRCA2 | c.4189G= (p.Glu1397=) c.3820G= (p.Glu1274=) n.4189G= | |
| 13 | g.32338544G>T | CA387780162 | BRCA2 | c.4189G>T (p.Glu1397Ter) c.3820G>T (p.Glu1274Ter) n.4189G>T | dbSNP |
| 13 | g.32338545A= | CA2082809269 | BRCA2 | c.4190A= (p.Glu1397=) c.3821A= (p.Glu1274=) n.4190A= | |
| 13 | g.32338545A>C | CA387780164 | BRCA2 | c.4190A>C (p.Glu1397Ala) c.3821A>C (p.Glu1274Ala) n.4190A>C | ClinVar dbSNP |
| 13 | g.32338545A>G | CA387780168 | BRCA2 | c.4190A>G (p.Glu1397Gly) c.3821A>G (p.Glu1274Gly) n.4190A>G | |
| 13 | g.32338545A>T | CA387780166 | BRCA2 | c.4190A>T (p.Glu1397Val) c.3821A>T (p.Glu1274Val) n.4190A>T | dbSNP |
| 13 | g.32338546A>C | CA387780169 | BRCA2 | c.4191A>C (p.Glu1397Asp) c.3822A>C (p.Glu1274Asp) n.4191A>C | |
| 13 | g.32338546A>G | CA483437902 | BRCA2 | c.4191A>G (p.Glu1397=) c.3822A>G (p.Glu1274=) n.4191A>G | |
| 13 | g.32338546A>T | CA387780171 | BRCA2 | c.4191A>T (p.Glu1397Asp) c.3822A>T (p.Glu1274Asp) n.4191A>T | dbSNP |
| 13 | g.32338547G>A | CA10579603 | BRCA2 | c.4192G>A (p.Ala1398Thr) c.3823G>A (p.Ala1275Thr) n.4192G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338547G>C | CA387780173 | BRCA2 | c.4192G>C (p.Ala1398Pro) c.3823G>C (p.Ala1275Pro) n.4192G>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338547G= | CA2082809276 | BRCA2 | c.4192G= (p.Ala1398=) c.3823G= (p.Ala1275=) n.4192G= | |
| 13 | g.32338547G>T | CA387780175 | BRCA2 | c.4192G>T (p.Ala1398Ser) c.3823G>T (p.Ala1275Ser) n.4192G>T | |
| 13 | g.32338548C>A | CA387780177 | BRCA2 | c.4193C>A (p.Ala1398Glu) c.3824C>A (p.Ala1275Glu) n.4193C>A | dbSNP gnomAD v4 |
| 13 | g.32338548C= | CA2082809284 | BRCA2 | c.4193C= (p.Ala1398=) c.3824C= (p.Ala1275=) n.4193C= | |
| 13 | g.32338548C>G | CA387780179 | BRCA2 | c.4193C>G (p.Ala1398Gly) c.3824C>G (p.Ala1275Gly) n.4193C>G | dbSNP |
| 13 | g.32338548C>T | CA387780180 | BRCA2 | c.4193C>T (p.Ala1398Val) c.3824C>T (p.Ala1275Val) n.4193C>T | ClinVar dbSNP |
| 13 | g.32338549A= | CA2082809289 | BRCA2 | c.4194A= (p.Ala1398=) c.3825A= (p.Ala1275=) n.4194A= | |
| 13 | g.32338549A>C | CA483437905 | BRCA2 | c.4194A>C (p.Ala1398=) c.3825A>C (p.Ala1275=) n.4194A>C | |
| 13 | g.32338549A>G | CA483437907 | BRCA2 | c.4194A>G (p.Ala1398=) c.3825A>G (p.Ala1275=) n.4194A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338549A>T | CA483437906 | BRCA2 | c.4194A>T (p.Ala1398=) c.3825A>T (p.Ala1275=) n.4194A>T | dbSNP |
| 13 | g.32338550T>A | CA387780181 | BRCA2 | c.4195T>A (p.Cys1399Ser) c.3826T>A (p.Cys1276Ser) n.4195T>A | dbSNP |
| 13 | g.32338550T>C | CA019706 | BRCA2 | c.4195T>C (p.Cys1399Arg) c.3826T>C (p.Cys1276Arg) n.4195T>C | ClinVar dbSNP |
| 13 | g.32338550T>G | CA387780185 | BRCA2 | c.4195T>G (p.Cys1399Gly) c.3826T>G (p.Cys1276Gly) n.4195T>G | |
| 13 | g.32338550T= | CA2082809295 | BRCA2 | c.4195T= (p.Cys1399=) c.3826T= (p.Cys1276=) n.4195T= | |
| 13 | g.32338551G>A | CA387780190 | BRCA2 | c.4196G>A (p.Cys1399Tyr) c.3827G>A (p.Cys1276Tyr) n.4196G>A | dbSNP |
| 13 | g.32338551G>C | CA387780187 | BRCA2 | c.4196G>C (p.Cys1399Ser) c.3827G>C (p.Cys1276Ser) n.4196G>C | dbSNP |
| 13 | g.32338551G= | CA2082809302 | BRCA2 | c.4196G= (p.Cys1399=) c.3827G= (p.Cys1276=) n.4196G= | |
| 13 | g.32338551G>T | CA6940759 | BRCA2 | c.4196G>T (p.Cys1399Phe) c.3827G>T (p.Cys1276Phe) n.4196G>T | ClinVar dbSNP ExAC gnomAD v2 |
| 13 | g.32338552T>A | CA387780191 | BRCA2 | c.4197T>A (p.Cys1399Ter) c.3828T>A (p.Cys1276Ter) n.4197T>A | ClinVar dbSNP |
| 13 | g.32338552T>C | CA483437909 | BRCA2 | c.4197T>C (p.Cys1399=) c.3828T>C (p.Cys1276=) n.4197T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338552T>G | CA387780193 | BRCA2 | c.4197T>G (p.Cys1399Trp) c.3828T>G (p.Cys1276Trp) n.4197T>G | dbSNP |
| 13 | g.32338552T= | CA2082809309 | BRCA2 | c.4197T= (p.Cys1399=) c.3828T= (p.Cys1276=) n.4197T= | |
| 13 | g.32338553C>A | CA387780195 | BRCA2 | c.4198C>A (p.His1400Asn) c.3829C>A (p.His1277Asn) n.4198C>A | dbSNP |
| 13 | g.32338553C= | CA2082809314 | BRCA2 | c.4198C= (p.His1400=) c.3829C= (p.His1277=) n.4198C= | |
| 13 | g.32338553C>G | CA387780197 | BRCA2 | c.4198C>G (p.His1400Asp) c.3829C>G (p.His1277Asp) n.4198C>G | dbSNP |
| 13 | g.32338553C>T | CA387780199 | BRCA2 | c.4198C>T (p.His1400Tyr) c.3829C>T (p.His1277Tyr) n.4198C>T | ClinVar dbSNP |
| 13 | g.32338554A= | CA2082809318 | BRCA2 | c.4199A= (p.His1400=) c.3830A= (p.His1277=) n.4199A= | |
| 13 | g.32338554A>C | CA387780201 | BRCA2 | c.4199A>C (p.His1400Pro) c.3830A>C (p.His1277Pro) n.4199A>C | |
| 13 | g.32338554A>G | CA387780202 | BRCA2 | c.4199A>G (p.His1400Arg) c.3830A>G (p.His1277Arg) n.4199A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338554A>T | CA387780207 | BRCA2 | c.4199A>T (p.His1400Leu) c.3830A>T (p.His1277Leu) n.4199A>T | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338555T>A | CA387780209 | BRCA2 | c.4200T>A (p.His1400Gln) c.3831T>A (p.His1277Gln) n.4200T>A | dbSNP |
| 13 | g.32338555T>C | CA483437913 | BRCA2 | c.4200T>C (p.His1400=) c.3831T>C (p.His1277=) n.4200T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338555T>G | CA387780211 | BRCA2 | c.4200T>G (p.His1400Gln) c.3831T>G (p.His1277Gln) n.4200T>G | dbSNP |
| 13 | g.32338555T= | CA2082809324 | BRCA2 | c.4200T= (p.His1400=) c.3831T= (p.His1277=) n.4200T= | |
| 13 | g.32338556G>A | CA387780213 | BRCA2 | c.4201G>A (p.Gly1401Ser) c.3832G>A (p.Gly1278Ser) n.4201G>A | ClinVar dbSNP |
| 13 | g.32338556G>C | CA387780215 | BRCA2 | c.4201G>C (p.Gly1401Arg) c.3832G>C (p.Gly1278Arg) n.4201G>C | dbSNP |
| 13 | g.32338556G= | CA2082809353 | BRCA2 | c.4201G= (p.Gly1401=) c.3832G= (p.Gly1278=) n.4201G= | |
| 13 | g.32338556G>T | CA387780216 | BRCA2 | c.4201G>T (p.Gly1401Cys) c.3832G>T (p.Gly1278Cys) n.4201G>T | dbSNP gnomAD v4 |
| 13 | g.32338557G>A | CA387780220 | BRCA2 | c.4202G>A (p.Gly1401Asp) c.3833G>A (p.Gly1278Asp) n.4202G>A | dbSNP |
| 13 | g.32338557G>C | CA019711 | BRCA2 | c.4202G>C (p.Gly1401Ala) c.3833G>C (p.Gly1278Ala) n.4202G>C | ClinVar dbSNP |
| 13 | g.32338557G= | CA2082809359 | BRCA2 | c.4202G= (p.Gly1401=) c.3833G= (p.Gly1278=) n.4202G= | |
| 13 | g.32338557G>T | CA387780218 | BRCA2 | c.4202G>T (p.Gly1401Val) c.3833G>T (p.Gly1278Val) n.4202G>T | dbSNP |
| 13 | g.32338558T>A | CA483437915 | BRCA2 | c.4203T>A (p.Gly1401=) c.3834T>A (p.Gly1278=) n.4203T>A | |
| 13 | g.32338558T>C | CA483437916 | BRCA2 | c.4203T>C (p.Gly1401=) c.3834T>C (p.Gly1278=) n.4203T>C | ClinVar dbSNP |
| 13 | g.32338558T>G | CA483437917 | BRCA2 | c.4203T>G (p.Gly1401=) c.3834T>G (p.Gly1278=) n.4203T>G | ClinVar |
| 13 | g.32338560_32338562dup | CA2622601020 | BRCA2 | c.4205_4207dup (p.Asn1402_Thr1403insAsn) c.3836_3838dup (p.Asn1279_Thr1280insAsn) n.4205_4207dup | gnomAD v4 |
| 13 | g.32338559A= | CA2082809368 | BRCA2 | c.4204A= (p.Asn1402=) c.3835A= (p.Asn1279=) n.4204A= | |
| 13 | g.32338559A>C | CA019715 | BRCA2 | c.4204A>C (p.Asn1402His) c.3835A>C (p.Asn1279His) n.4204A>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338559A>G | CA387780223 | BRCA2 | c.4204A>G (p.Asn1402Asp) c.3835A>G (p.Asn1279Asp) n.4204A>G | dbSNP |
| 13 | g.32338559A>T | CA387780225 | BRCA2 | c.4204A>T (p.Asn1402Tyr) c.3835A>T (p.Asn1279Tyr) n.4204A>T | dbSNP |
| 13 | g.32338560A>C | CA387780227 | BRCA2 | c.4205A>C (p.Asn1402Thr) c.3836A>C (p.Asn1279Thr) n.4205A>C | |
| 13 | g.32338560A>G | CA387780230 | BRCA2 | c.4205A>G (p.Asn1402Ser) c.3836A>G (p.Asn1279Ser) n.4205A>G | ClinVar dbSNP |
| 13 | g.32338560A>T | CA387780233 | BRCA2 | c.4205A>T (p.Asn1402Ile) c.3836A>T (p.Asn1279Ile) n.4205A>T | dbSNP |
| 13 | g.32338561T>A | CA387780235 | BRCA2 | c.4206T>A (p.Asn1402Lys) c.3837T>A (p.Asn1279Lys) n.4206T>A | dbSNP |
| 13 | g.32338561T>C | CA10583101 | BRCA2 | c.4206T>C (p.Asn1402=) c.3837T>C (p.Asn1279=) n.4206T>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338561T>G | CA387780238 | BRCA2 | c.4206T>G (p.Asn1402Lys) c.3837T>G (p.Asn1279Lys) n.4206T>G | dbSNP |
| 13 | g.32338561T= | CA2082809375 | BRCA2 | c.4206T= (p.Asn1402=) c.3837T= (p.Asn1279=) n.4206T= | |
| 13 | g.32338562_32338564del | CA2499222157 | BRCA2 | c.4207_4209del (p.Thr1403del) c.3838_3840del (p.Thr1280del) n.4207_4209del | ClinVar dbSNP |
| 13 | g.32338562A= | CA2082809382 | BRCA2 | c.4207A= (p.Thr1403=) c.3838A= (p.Thr1280=) n.4207A= | |
| 13 | g.32338562A>C | CA387780240 | BRCA2 | c.4207A>C (p.Thr1403Pro) c.3838A>C (p.Thr1280Pro) n.4207A>C | dbSNP |
| 13 | g.32338562A>G | CA387780242 | BRCA2 | c.4207A>G (p.Thr1403Ala) c.3838A>G (p.Thr1280Ala) n.4207A>G | ClinVar dbSNP |
| 13 | g.32338562A>T | CA387780244 | BRCA2 | c.4207A>T (p.Thr1403Ser) c.3838A>T (p.Thr1280Ser) n.4207A>T | dbSNP |
| 13 | g.32338562dup | CA2499222158 | BRCA2 | c.4207dup (p.Thr1403AsnfsTer4) c.3838dup (p.Thr1280AsnfsTer4) n.4207dup | |
| 13 | g.32338562_32338565delinsACTT | CA2082809385 | BRCA2 | c.4207_4210delinsACTT (p.Thr1403=) c.3838_3841delinsACTT (p.Thr1280=) n.4207_4210delinsACTT | |
| 13 | g.32338563_32338567del | CA2499222159 | BRCA2 | c.4208_4212del (p.Thr1403LysfsTer2) c.3839_3843del (p.Thr1280LysfsTer2) n.4208_4212del | ClinVar dbSNP |
| 13 | g.32338563C>A | CA387780246 | BRCA2 | c.4208C>A (p.Thr1403Asn) c.3839C>A (p.Thr1280Asn) n.4208C>A | dbSNP |
| 13 | g.32338563C= | CA2082809403 | BRCA2 | c.4208C= (p.Thr1403=) c.3839C= (p.Thr1280=) n.4208C= | |
| 13 | g.32338563C>G | CA387780250 | BRCA2 | c.4208C>G (p.Thr1403Ser) c.3839C>G (p.Thr1280Ser) n.4208C>G | ClinVar dbSNP COSMIC COSMIC |
| 13 | g.32338563C>T | CA387780248 | BRCA2 | c.4208C>T (p.Thr1403Ile) c.3839C>T (p.Thr1280Ile) n.4208C>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338564_32338566del | CA2082809396 | BRCA2 | c.4209_4211del (p.Ser1404del) c.3840_3842del (p.Ser1281del) n.4209_4211del | ClinVar dbSNP |
| 13 | g.32338564T>A | CA483437930 | BRCA2 | c.4209T>A (p.Thr1403=) c.3840T>A (p.Thr1280=) n.4209T>A | ClinVar dbSNP |
| 13 | g.32338564T>C | CA483437926 | BRCA2 | c.4209T>C (p.Thr1403=) c.3840T>C (p.Thr1280=) n.4209T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338564T>G | CA483437929 | BRCA2 | c.4209T>G (p.Thr1403=) c.3840T>G (p.Thr1280=) n.4209T>G | |
| 13 | g.32338564T= | CA2082809412 | BRCA2 | c.4209T= (p.Thr1403=) c.3840T= (p.Thr1280=) n.4209T= | |
| 13 | g.32338564_32338569delinsTTCAAA | CA2082809415 | BRCA2 | c.4209_4214delinsTTCAAA (p.Thr1403=) c.3840_3845delinsTTCAAA (p.Thr1280=) n.4209_4214delinsTTCAAA | |
| 13 | g.32338565T>A | CA387780252 | BRCA2 | c.4210T>A (p.Ser1404Thr) c.3841T>A (p.Ser1281Thr) n.4210T>A | dbSNP |
| 13 | g.32338565T>C | CA387780257 | BRCA2 | c.4210T>C (p.Ser1404Pro) c.3841T>C (p.Ser1281Pro) n.4210T>C | |
| 13 | g.32338565T>G | CA387780255 | BRCA2 | c.4210T>G (p.Ser1404Ala) c.3841T>G (p.Ser1281Ala) n.4210T>G | |
| 13 | g.32338565_32338566delinsTC | CA2082809420 | BRCA2 | c.4210_4211delinsTC (p.Ser1404=) c.3841_3842delinsTC (p.Ser1281=) n.4210_4211delinsTC | |
| 13 | g.32338566_32338570del | CA019721 | BRCA2 | c.4211_4215del (p.Ser1404Ter) c.3842_3846del (p.Ser1281Ter) n.4211_4215del | ClinVar dbSNP |
| 13 | g.32338566del | CA019731 | BRCA2 | c.4211del (p.Ser1404Ter) c.3842del (p.Ser1281Ter) n.4211del | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338566C>A | CA387780259 | BRCA2 | c.4211C>A (p.Ser1404Ter) c.3842C>A (p.Ser1281Ter) n.4211C>A | ClinVar dbSNP |
| 13 | g.32338566C= | CA2082809467 | BRCA2 | c.4211C= (p.Ser1404=) c.3842C= (p.Ser1281=) n.4211C= | |
| 13 | g.32338566C>G | CA10589245 | BRCA2 | c.4211C>G (p.Ser1404Ter) c.3842C>G (p.Ser1281Ter) n.4211C>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338566C>T | CA019726 | BRCA2 | c.4211C>T (p.Ser1404Leu) c.3842C>T (p.Ser1281Leu) n.4211C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338567A>C | CA483437934 | BRCA2 | c.4212A>C (p.Ser1404=) c.3843A>C (p.Ser1281=) n.4212A>C | ClinVar |
| 13 | g.32338567A>G | CA483437935 | BRCA2 | c.4212A>G (p.Ser1404=) c.3843A>G (p.Ser1281=) n.4212A>G | |
| 13 | g.32338567A>T | CA483437936 | BRCA2 | c.4212A>T (p.Ser1404=) c.3843A>T (p.Ser1281=) n.4212A>T | dbSNP |
| 13 | g.32338569_32338573del | CA2695199717 | BRCA2 | c.4214_4218del (p.Asn1405ArgfsTer7) c.3845_3849del (p.Asn1282ArgfsTer7) n.4214_4218del | ClinVar |
| 13 | g.32338568A= | CA2082809486 | BRCA2 | c.4213A= (p.Asn1405=) c.3844A= (p.Asn1282=) n.4213A= | |
| 13 | g.32338568A>C | CA387780266 | BRCA2 | c.4213A>C (p.Asn1405His) c.3844A>C (p.Asn1282His) n.4213A>C | ClinVar dbSNP |
| 13 | g.32338568A>G | CA387780264 | BRCA2 | c.4213A>G (p.Asn1405Asp) c.3844A>G (p.Asn1282Asp) n.4213A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338568A>T | CA387780268 | BRCA2 | c.4213A>T (p.Asn1405Tyr) c.3844A>T (p.Asn1282Tyr) n.4213A>T | dbSNP |
| 13 | g.32338569A>C | CA387780270 | BRCA2 | c.4214A>C (p.Asn1405Thr) c.3845A>C (p.Asn1282Thr) n.4214A>C | |
| 13 | g.32338569A>G | CA387780274 | BRCA2 | c.4214A>G (p.Asn1405Ser) c.3845A>G (p.Asn1282Ser) n.4214A>G | ClinVar dbSNP |
| 13 | g.32338569A>T | CA387780272 | BRCA2 | c.4214A>T (p.Asn1405Ile) c.3845A>T (p.Asn1282Ile) n.4214A>T | dbSNP |
| 13 | g.32338570T>A | CA387780275 | BRCA2 | c.4215T>A (p.Asn1405Lys) c.3846T>A (p.Asn1282Lys) n.4215T>A | ClinVar |
| 13 | g.32338570T>C | CA483437938 | BRCA2 | c.4215T>C (p.Asn1405=) c.3846T>C (p.Asn1282=) n.4215T>C | |
| 13 | g.32338570T>G | CA387780277 | BRCA2 | c.4215T>G (p.Asn1405Lys) c.3846T>G (p.Asn1282Lys) n.4215T>G | |
| 13 | g.32338570_32338573delinsTAAA | CA2082809497 | BRCA2 | c.4215_4218delinsTAAA (p.Asn1405=) c.3846_3849delinsTAAA (p.Asn1282=) n.4215_4218delinsTAAA | |
| 13 | g.32338570_32338574delinsTAAAG | CA2082809500 | BRCA2 | c.4215_4219delinsTAAAG (p.Asn1405=) c.3846_3850delinsTAAAG (p.Asn1282=) n.4215_4219delinsTAAAG | |
| 13 | g.32338571A= | CA2082809528 | BRCA2 | c.4216A= (p.Lys1406=) c.3847A= (p.Lys1283=) n.4216A= | |
| 13 | g.32338571A>C | CA387780278 | BRCA2 | c.4216A>C (p.Lys1406Gln) c.3847A>C (p.Lys1283Gln) n.4216A>C | |
| 13 | g.32338571A>G | CA10579604 | BRCA2 | c.4216A>G (p.Lys1406Glu) c.3847A>G (p.Lys1283Glu) n.4216A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338571A>T | CA387780281 | BRCA2 | c.4216A>T (p.Lys1406Ter) c.3847A>T (p.Lys1283Ter) n.4216A>T | dbSNP |
| 13 | g.32338571_32338573del | CA019735 | BRCA2 | c.4216_4218del (p.Lys1406del) c.3847_3849del (p.Lys1283del) n.4216_4218del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338573_32338576del | CA019739 | BRCA2 | c.4218_4221del (p.Lys1406AsnfsTer3) c.3849_3852del (p.Lys1283AsnfsTer3) n.4218_4221del | ClinVar dbSNP gnomAD v4 COSMIC |
| 13 | g.32338572A>C | CA387780285 | BRCA2 | c.4217A>C (p.Lys1406Thr) c.3848A>C (p.Lys1283Thr) n.4217A>C | |
| 13 | g.32338572A>G | CA387780287 | BRCA2 | c.4217A>G (p.Lys1406Arg) c.3848A>G (p.Lys1283Arg) n.4217A>G | |
| 13 | g.32338572A>T | CA387780288 | BRCA2 | c.4217A>T (p.Lys1406Ile) c.3848A>T (p.Lys1283Ile) n.4217A>T | dbSNP |
| 13 | g.32338573A= | CA2082809535 | BRCA2 | c.4218A= (p.Lys1406=) c.3849A= (p.Lys1283=) n.4218A= | |
| 13 | g.32338573A>C | CA387780291 | BRCA2 | c.4218A>C (p.Lys1406Asn) c.3849A>C (p.Lys1283Asn) n.4218A>C | ClinVar dbSNP |
| 13 | g.32338573A>G | CA483437942 | BRCA2 | c.4218A>G (p.Lys1406=) c.3849A>G (p.Lys1283=) n.4218A>G | ClinVar dbSNP |
| 13 | g.32338573A>T | CA387780292 | BRCA2 | c.4218A>T (p.Lys1406Asn) c.3849A>T (p.Lys1283Asn) n.4218A>T | dbSNP |
| 13 | g.32338574G>A | CA387780294 | BRCA2 | c.4219G>A (p.Glu1407Lys) c.3850G>A (p.Glu1284Lys) n.4219G>A | dbSNP |
| 13 | g.32338574G>C | CA387780298 | BRCA2 | c.4219G>C (p.Glu1407Gln) c.3850G>C (p.Glu1284Gln) n.4219G>C | dbSNP COSMIC COSMIC |
| 13 | g.32338574G>T | CA387780296 | BRCA2 | c.4219G>T (p.Glu1407Ter) c.3850G>T (p.Glu1284Ter) n.4219G>T | ClinVar dbSNP |
| 13 | g.32338574_32338575delinsGA | CA2082809546 | BRCA2 | c.4219_4220delinsGA (p.Glu1407=) c.3850_3851delinsGA (p.Glu1284=) n.4219_4220delinsGA | |
| 13 | g.32338575A= | CA2082809563 | BRCA2 | c.4220A= (p.Glu1407=) c.3851A= (p.Glu1284=) n.4220A= | |
| 13 | g.32338575A>C | CA387780300 | BRCA2 | c.4220A>C (p.Glu1407Ala) c.3851A>C (p.Glu1284Ala) n.4220A>C | |
| 13 | g.32338575A>G | CA387780302 | BRCA2 | c.4220A>G (p.Glu1407Gly) c.3851A>G (p.Glu1284Gly) n.4220A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338575A>T | CA387780304 | BRCA2 | c.4220A>T (p.Glu1407Val) c.3851A>T (p.Glu1284Val) n.4220A>T | ClinVar dbSNP |
| 13 | g.32338576del | CA10589246 | BRCA2 | c.4221del (p.Glu1407AspfsTer3) c.3852del (p.Glu1284AspfsTer3) n.4221del | ClinVar dbSNP |
| 13 | g.32338576A>C | CA387780307 | BRCA2 | c.4221A>C (p.Glu1407Asp) c.3852A>C (p.Glu1284Asp) n.4221A>C | dbSNP |
| 13 | g.32338576A>G | CA483437948 | BRCA2 | c.4221A>G (p.Glu1407=) c.3852A>G (p.Glu1284=) n.4221A>G | dbSNP |
| 13 | g.32338576A>T | CA387780309 | BRCA2 | c.4221A>T (p.Glu1407Asp) c.3852A>T (p.Glu1284Asp) n.4221A>T | dbSNP |
| 13 | g.32338577_32338578del | CA2580087261 | BRCA2 | c.4222_4223del (p.Gln1408ValfsTer5) c.3853_3854del (p.Gln1285ValfsTer5) n.4222_4223del | ClinVar |
| 13 | g.32338577C>A | CA387780311 | BRCA2 | c.4222C>A (p.Gln1408Lys) c.3853C>A (p.Gln1285Lys) n.4222C>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338577C= | CA2082809588 | BRCA2 | c.4222C= (p.Gln1408=) c.3853C= (p.Gln1285=) n.4222C= | |
| 13 | g.32338577C>G | CA387780313 | BRCA2 | c.4222C>G (p.Gln1408Glu) c.3853C>G (p.Gln1285Glu) n.4222C>G | dbSNP gnomAD v4 |
| 13 | g.32338577C>T | CA019744 | BRCA2 | c.4222C>T (p.Gln1408Ter) c.3853C>T (p.Gln1285Ter) n.4222C>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338577dup | CA2573149372 | BRCA2 | c.4222dup (p.Gln1408ProfsTer6) c.3853dup (p.Gln1285ProfsTer6) n.4222dup | ClinVar dbSNP |
| 13 | g.32338577_32338578delinsCA | CA2082809581 | BRCA2 | c.4222_4223delinsCA (p.Gln1408=) c.3853_3854delinsCA (p.Gln1285=) n.4222_4223delinsCA | |
| 13 | g.32338577_32338581delinsCAGTT | CA2082809578 | BRCA2 | c.4222_4226delinsCAGTT (p.Gln1408=) c.3853_3857delinsCAGTT (p.Gln1285=) n.4222_4226delinsCAGTT | |
| 13 | g.32338578del | CA019749 | BRCA2 | c.4223del (p.Gln1408ArgfsTer2) c.3854del (p.Gln1285ArgfsTer2) n.4223del | ClinVar dbSNP |
| 13 | g.32338578A= | CA2082809603 | BRCA2 | c.4223A= (p.Gln1408=) c.3854A= (p.Gln1285=) n.4223A= | |
| 13 | g.32338578A>C | CA387780320 | BRCA2 | c.4223A>C (p.Gln1408Pro) c.3854A>C (p.Gln1285Pro) n.4223A>C | |
| 13 | g.32338578A>G | CA6940760 | BRCA2 | c.4223A>G (p.Gln1408Arg) c.3854A>G (p.Gln1285Arg) n.4223A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338578A>T | CA387780318 | BRCA2 | c.4223A>T (p.Gln1408Leu) c.3854A>T (p.Gln1285Leu) n.4223A>T | dbSNP |
| 13 | g.32338579_32338582del | CA954694064 | BRCA2 | c.4224_4227del (p.Thr1410LeufsTer8) c.3855_3858del (p.Thr1287LeufsTer8) n.4224_4227del | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338579G>A | CA337867 | BRCA2 | c.4224G>A (p.Gln1408=) c.3855G>A (p.Gln1285=) n.4224G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338579G>C | CA387780322 | BRCA2 | c.4224G>C (p.Gln1408His) c.3855G>C (p.Gln1285His) n.4224G>C | |
| 13 | g.32338579G= | CA2082809612 | BRCA2 | c.4224G= (p.Gln1408=) c.3855G= (p.Gln1285=) n.4224G= | |
| 13 | g.32338579G>T | CA387780324 | BRCA2 | c.4224G>T (p.Gln1408His) c.3855G>T (p.Gln1285His) n.4224G>T |