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New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32338631_32338641del | CA2843744725 | BRCA2 | c.4276_4286del (p.Thr1426AspfsTer8) c.3907_3917del (p.Thr1303AspfsTer8) n.4276_4286del | |
| 13 | g.32338639dup | CA019907 | BRCA2 | c.4284dup (p.Gln1429SerfsTer9) c.3915dup (p.Gln1306SerfsTer9) n.4284dup | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338639del | CA658823573 | BRCA2 | c.4284del (p.Gln1429ArgfsTer19) c.3915del (p.Gln1306ArgfsTer19) n.4284del | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338639T>A | CA387780626 | BRCA2 | c.4284T>A (p.Phe1428Leu) c.3915T>A (p.Phe1305Leu) n.4284T>A | dbSNP |
| 13 | g.32338639T>C | CA483438142 | BRCA2 | c.4284T>C (p.Phe1428=) c.3915T>C (p.Phe1305=) n.4284T>C | dbSNP |
| 13 | g.32338639T>G | CA387780630 | BRCA2 | c.4284T>G (p.Phe1428Leu) c.3915T>G (p.Phe1305Leu) n.4284T>G | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338639T= | CA2082810176 | BRCA2 | c.4284T= (p.Phe1428=) c.3915T= (p.Phe1305=) n.4284T= | |
| 13 | g.32338640C>A | CA387780632 | BRCA2 | c.4285C>A (p.Gln1429Lys) c.3916C>A (p.Gln1306Lys) n.4285C>A | dbSNP gnomAD v4 |
| 13 | g.32338640C= | CA2082810205 | BRCA2 | c.4285C= (p.Gln1429=) c.3916C= (p.Gln1306=) n.4285C= | |
| 13 | g.32338640C>G | CA387780634 | BRCA2 | c.4285C>G (p.Gln1429Glu) c.3916C>G (p.Gln1306Glu) n.4285C>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338640C>T | CA019916 | BRCA2 | c.4285C>T (p.Gln1429Ter) c.3916C>T (p.Gln1306Ter) n.4285C>T | ClinVar dbSNP |
| 13 | g.32338640dup | CA2499222162 | BRCA2 | c.4285dup (p.Gln1429ProfsTer9) c.3916dup (p.Gln1306ProfsTer9) n.4285dup | |
| 13 | g.32338640_32338641insT | CA10589249 | BRCA2 | c.4285_4286insT (p.Gln1429LeufsTer9) c.3916_3917insT (p.Gln1306LeufsTer9) n.4285_4286insT | ClinVar dbSNP |
| 13 | g.32338641A>C | CA387780640 | BRCA2 | c.4286A>C (p.Gln1429Pro) c.3917A>C (p.Gln1306Pro) n.4286A>C | |
| 13 | g.32338641A>G | CA387780638 | BRCA2 | c.4286A>G (p.Gln1429Arg) c.3917A>G (p.Gln1306Arg) n.4286A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338641A>T | CA387780639 | BRCA2 | c.4286A>T (p.Gln1429Leu) c.3917A>T (p.Gln1306Leu) n.4286A>T | dbSNP |
| 13 | g.32338642G>A | CA483438145 | BRCA2 | c.4287G>A (p.Gln1429=) c.3918G>A (p.Gln1306=) n.4287G>A | dbSNP |
| 13 | g.32338642G>C | CA387780641 | BRCA2 | c.4287G>C (p.Gln1429His) c.3918G>C (p.Gln1306His) n.4287G>C | dbSNP gnomAD v4 |
| 13 | g.32338642G= | CA2082810225 | BRCA2 | c.4287G= (p.Gln1429=) c.3918G= (p.Gln1306=) n.4287G= | |
| 13 | g.32338642G>T | CA387780642 | BRCA2 | c.4287G>T (p.Gln1429His) c.3918G>T (p.Gln1306His) n.4287G>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338643A= | CA2082810228 | BRCA2 | c.4288A= (p.Thr1430=) c.3919A= (p.Thr1307=) n.4288A= | |
| 13 | g.32338643A>C | CA387780643 | BRCA2 | c.4288A>C (p.Thr1430Pro) c.3919A>C (p.Thr1307Pro) n.4288A>C | |
| 13 | g.32338643A>G | CA387780645 | BRCA2 | c.4288A>G (p.Thr1430Ala) c.3919A>G (p.Thr1307Ala) n.4288A>G | ClinVar dbSNP |
| 13 | g.32338643A>T | CA387780647 | BRCA2 | c.4288A>T (p.Thr1430Ser) c.3919A>T (p.Thr1307Ser) n.4288A>T | dbSNP |
| 13 | g.32338644C>A | CA387780651 | BRCA2 | c.4289C>A (p.Thr1430Asn) c.3920C>A (p.Thr1307Asn) n.4289C>A | dbSNP |
| 13 | g.32338644C= | CA2082810235 | BRCA2 | c.4289C= (p.Thr1430=) c.3920C= (p.Thr1307=) n.4289C= | |
| 13 | g.32338644C>G | CA387780656 | BRCA2 | c.4289C>G (p.Thr1430Ser) c.3920C>G (p.Thr1307Ser) n.4289C>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338644C>T | CA10579607 | BRCA2 | c.4289C>T (p.Thr1430Ile) c.3920C>T (p.Thr1307Ile) n.4289C>T | ClinVar dbSNP |
| 13 | g.32338645T>A | CA483438147 | BRCA2 | c.4290T>A (p.Thr1430=) c.3921T>A (p.Thr1307=) n.4290T>A | dbSNP |
| 13 | g.32338645T>C | CA483438149 | BRCA2 | c.4290T>C (p.Thr1430=) c.3921T>C (p.Thr1307=) n.4290T>C | ClinVar dbSNP |
| 13 | g.32338645T>G | CA483438151 | BRCA2 | c.4290T>G (p.Thr1430=) c.3921T>G (p.Thr1307=) n.4290T>G | ClinVar gnomAD v4 |
| 13 | g.32338645T= | CA2082810245 | BRCA2 | c.4290T= (p.Thr1430=) c.3921T= (p.Thr1307=) n.4290T= | |
| 13 | g.32338646G>A | CA387780658 | BRCA2 | c.4291G>A (p.Ala1431Thr) c.3922G>A (p.Ala1308Thr) n.4291G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338646G>C | CA387780659 | BRCA2 | c.4291G>C (p.Ala1431Pro) c.3922G>C (p.Ala1308Pro) n.4291G>C | ClinVar dbSNP |
| 13 | g.32338646G>T | CA387780662 | BRCA2 | c.4291G>T (p.Ala1431Ser) c.3922G>T (p.Ala1308Ser) n.4291G>T | |
| 13 | g.32338647C>A | CA387780676 | BRCA2 | c.4292C>A (p.Ala1431Glu) c.3923C>A (p.Ala1308Glu) n.4292C>A | dbSNP gnomAD v4 |
| 13 | g.32338647C= | CA2082810255 | BRCA2 | c.4292C= (p.Ala1431=) c.3923C= (p.Ala1308=) n.4292C= | |
| 13 | g.32338647C>G | CA387780675 | BRCA2 | c.4292C>G (p.Ala1431Gly) c.3923C>G (p.Ala1308Gly) n.4292C>G | dbSNP |
| 13 | g.32338647C>T | CA10579608 | BRCA2 | c.4292C>T (p.Ala1431Val) c.3923C>T (p.Ala1308Val) n.4292C>T | ClinVar dbSNP |
| 13 | g.32338648A= | CA2082810263 | BRCA2 | c.4293A= (p.Ala1431=) c.3924A= (p.Ala1308=) n.4293A= | |
| 13 | g.32338648A>C | CA483438154 | BRCA2 | c.4293A>C (p.Ala1431=) c.3924A>C (p.Ala1308=) n.4293A>C | |
| 13 | g.32338648A>G | CA019925 | BRCA2 | c.4293A>G (p.Ala1431=) c.3924A>G (p.Ala1308=) n.4293A>G | ClinVar dbSNP |
| 13 | g.32338648A>T | CA483438155 | BRCA2 | c.4293A>T (p.Ala1431=) c.3924A>T (p.Ala1308=) n.4293A>T | |
| 13 | g.32338649A= | CA2082810270 | BRCA2 | c.4294A= (p.Ser1432=) c.3925A= (p.Ser1309=) n.4294A= | |
| 13 | g.32338649A>C | CA387780677 | BRCA2 | c.4294A>C (p.Ser1432Arg) c.3925A>C (p.Ser1309Arg) n.4294A>C | |
| 13 | g.32338649A>G | CA019930 | BRCA2 | c.4294A>G (p.Ser1432Gly) c.3925A>G (p.Ser1309Gly) n.4294A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338649A>T | CA387780678 | BRCA2 | c.4294A>T (p.Ser1432Cys) c.3925A>T (p.Ser1309Cys) n.4294A>T | dbSNP |
| 13 | g.32338650G>A | CA387780679 | BRCA2 | c.4295G>A (p.Ser1432Asn) c.3926G>A (p.Ser1309Asn) n.4295G>A | ClinVar dbSNP |
| 13 | g.32338650G>C | CA387780681 | BRCA2 | c.4295G>C (p.Ser1432Thr) c.3926G>C (p.Ser1309Thr) n.4295G>C | dbSNP |
| 13 | g.32338650G= | CA2082810278 | BRCA2 | c.4295G= (p.Ser1432=) c.3926G= (p.Ser1309=) n.4295G= | |
| 13 | g.32338650G>T | CA387780683 | BRCA2 | c.4295G>T (p.Ser1432Ile) c.3926G>T (p.Ser1309Ile) n.4295G>T | dbSNP |
| 13 | g.32338651T>A | CA387780685 | BRCA2 | c.4296T>A (p.Ser1432Arg) c.3927T>A (p.Ser1309Arg) n.4296T>A | ClinVar |
| 13 | g.32338651T>C | CA483438159 | BRCA2 | c.4296T>C (p.Ser1432=) c.3927T>C (p.Ser1309=) n.4296T>C | |
| 13 | g.32338651T>G | CA16619704 | BRCA2 | c.4296T>G (p.Ser1432Arg) c.3927T>G (p.Ser1309Arg) n.4296T>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338651T= | CA2082810284 | BRCA2 | c.4296T= (p.Ser1432=) c.3927T= (p.Ser1309=) n.4296T= | |
| 13 | g.32338652G>A | CA387780694 | BRCA2 | c.4297G>A (p.Gly1433Arg) c.3928G>A (p.Gly1310Arg) n.4297G>A | gnomAD v4 COSMIC COSMIC |
| 13 | g.32338652G>C | CA387780696 | BRCA2 | c.4297G>C (p.Gly1433Arg) c.3928G>C (p.Gly1310Arg) n.4297G>C | |
| 13 | g.32338652G= | CA2082810290 | BRCA2 | c.4297G= (p.Gly1433=) c.3928G= (p.Gly1310=) n.4297G= | |
| 13 | g.32338652G>T | CA247507454 | BRCA2 | c.4297G>T (p.Gly1433Trp) c.3928G>T (p.Gly1310Trp) n.4297G>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338653G>A | CA6940767 | BRCA2 | c.4298G>A (p.Gly1433Glu) c.3929G>A (p.Gly1310Glu) n.4298G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338653G>C | CA387780700 | BRCA2 | c.4298G>C (p.Gly1433Ala) c.3929G>C (p.Gly1310Ala) n.4298G>C | dbSNP |
| 13 | g.32338653G= | CA2082810302 | BRCA2 | c.4298G= (p.Gly1433=) c.3929G= (p.Gly1310=) n.4298G= | |
| 13 | g.32338653G>T | CA387780703 | BRCA2 | c.4298G>T (p.Gly1433Val) c.3929G>T (p.Gly1310Val) n.4298G>T | ClinVar dbSNP |
| 13 | g.32338654G>A | CA483438163 | BRCA2 | c.4299G>A (p.Gly1433=) c.3930G>A (p.Gly1310=) n.4299G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338654G>C | CA483438160 | BRCA2 | c.4299G>C (p.Gly1433=) c.3930G>C (p.Gly1310=) n.4299G>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338654G= | CA2082810320 | BRCA2 | c.4299G= (p.Gly1433=) c.3930G= (p.Gly1310=) n.4299G= | |
| 13 | g.32338654G>T | CA483438162 | BRCA2 | c.4299G>T (p.Gly1433=) c.3930G>T (p.Gly1310=) n.4299G>T | ClinVar dbSNP |
| 13 | g.32338654_32338655delinsGA | CA2082810324 | BRCA2 | c.4299_4300delinsGA (p.Gly1433=) c.3930_3931delinsGA (p.Gly1310=) n.4299_4300delinsGA | |
| 13 | g.32338655A= | CA2082810336 | BRCA2 | c.4300A= (p.Lys1434=) c.3931A= (p.Lys1311=) n.4300A= | |
| 13 | g.32338655A>C | CA387780708 | BRCA2 | c.4300A>C (p.Lys1434Gln) c.3931A>C (p.Lys1311Gln) n.4300A>C | |
| 13 | g.32338655A>G | CA10579609 | BRCA2 | c.4300A>G (p.Lys1434Glu) c.3931A>G (p.Lys1311Glu) n.4300A>G | ClinVar dbSNP |
| 13 | g.32338655A>T | CA387780710 | BRCA2 | c.4300A>T (p.Lys1434Ter) c.3931A>T (p.Lys1311Ter) n.4300A>T | dbSNP |
| 13 | g.32338659dup | CA2697551733 | BRCA2 | c.4304dup (p.Asn1435LysfsTer3) c.3935dup (p.Asn1312LysfsTer3) n.4304dup | ClinVar |
| 13 | g.32338659del | CA10589250 | BRCA2 | c.4304del (p.Asn1435IlefsTer13) c.3935del (p.Asn1312IlefsTer13) n.4304del | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338656A= | CA2082810351 | BRCA2 | c.4301A= (p.Lys1434=) c.3932A= (p.Lys1311=) n.4301A= | |
| 13 | g.32338656A>C | CA387780713 | BRCA2 | c.4301A>C (p.Lys1434Thr) c.3932A>C (p.Lys1311Thr) n.4301A>C | |
| 13 | g.32338656A>G | CA387780714 | BRCA2 | c.4301A>G (p.Lys1434Arg) c.3932A>G (p.Lys1311Arg) n.4301A>G | dbSNP |
| 13 | g.32338656A>T | CA019939 | BRCA2 | c.4301A>T (p.Lys1434Ile) c.3932A>T (p.Lys1311Ile) n.4301A>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338657A>C | CA387780717 | BRCA2 | c.4302A>C (p.Lys1434Asn) c.3933A>C (p.Lys1311Asn) n.4302A>C | |
| 13 | g.32338657A>G | CA483438168 | BRCA2 | c.4302A>G (p.Lys1434=) c.3933A>G (p.Lys1311=) n.4302A>G | ClinVar dbSNP |
| 13 | g.32338657A>T | CA387780718 | BRCA2 | c.4302A>T (p.Lys1434Asn) c.3933A>T (p.Lys1311Asn) n.4302A>T | dbSNP |
| 13 | g.32338658A>C | CA387780719 | BRCA2 | c.4303A>C (p.Asn1435His) c.3934A>C (p.Asn1312His) n.4303A>C | |
| 13 | g.32338658A>G | CA387780721 | BRCA2 | c.4303A>G (p.Asn1435Asp) c.3934A>G (p.Asn1312Asp) n.4303A>G | |
| 13 | g.32338658A>T | CA387780730 | BRCA2 | c.4303A>T (p.Asn1435Tyr) c.3934A>T (p.Asn1312Tyr) n.4303A>T | |
| 13 | g.32338658_32338660delinsAAT | CA2082810360 | BRCA2 | c.4303_4305delinsAAT (p.Asn1435=) c.3934_3936delinsAAT (p.Asn1312=) n.4303_4305delinsAAT | |
| 13 | g.32338658_32338663delinsAATATT | CA2082810361 | BRCA2 | c.4303_4308delinsAATATT (p.Asn1435=) c.3934_3939delinsAATATT (p.Asn1312=) n.4303_4308delinsAATATT | |
| 13 | g.32338659A>C | CA387780741 | BRCA2 | c.4304A>C (p.Asn1435Thr) c.3935A>C (p.Asn1312Thr) n.4304A>C | COSMIC COSMIC |
| 13 | g.32338659A>G | CA387780736 | BRCA2 | c.4304A>G (p.Asn1435Ser) c.3935A>G (p.Asn1312Ser) n.4304A>G | dbSNP |
| 13 | g.32338659A>T | CA387780738 | BRCA2 | c.4304A>T (p.Asn1435Ile) c.3935A>T (p.Asn1312Ile) n.4304A>T | |
| 13 | g.32338659_32338660delinsAT | CA2082810388 | BRCA2 | c.4304_4305delinsAT (p.Asn1435=) c.3935_3936delinsAT (p.Asn1312=) n.4304_4305delinsAT | |
| 13 | g.32338659_32338662delinsATAT | CA2082810391 | BRCA2 | c.4304_4307delinsATAT (p.Asn1435=) c.3935_3938delinsATAT (p.Asn1312=) n.4304_4307delinsATAT | |
| 13 | g.32338661_32338662del | CA10589252 | BRCA2 | c.4306_4307del (p.Ile1436Ter) c.3937_3938del (p.Ile1313Ter) n.4306_4307del | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338660_32338664del | CA913190946 | BRCA2 | c.4305_4309del (p.Asn1435LysfsTer8) c.3936_3940del (p.Asn1312LysfsTer8) n.4305_4309del | ClinVar dbSNP |
| 13 | g.32338660del | CA10589251 | BRCA2 | c.4305del (p.Asn1435LysfsTer13) c.3936del (p.Asn1312LysfsTer13) n.4305del | ClinVar dbSNP |
| 13 | g.32338660T>A | CA387780745 | BRCA2 | c.4305T>A (p.Asn1435Lys) c.3936T>A (p.Asn1312Lys) n.4305T>A | dbSNP |
| 13 | g.32338660T>C | CA483438172 | BRCA2 | c.4305T>C (p.Asn1435=) c.3936T>C (p.Asn1312=) n.4305T>C | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338660T>G | CA10583104 | BRCA2 | c.4305T>G (p.Asn1435Lys) c.3936T>G (p.Asn1312Lys) n.4305T>G | ClinVar dbSNP |
| 13 | g.32338660T= | CA2082810408 | BRCA2 | c.4305T= (p.Asn1435=) c.3936T= (p.Asn1312=) n.4305T= | |
| 13 | g.32338662_32338664del | CA916080548 | BRCA2 | c.4307_4309del (p.Ile1436del) c.3938_3940del (p.Ile1313del) n.4307_4309del | ClinVar dbSNP |
| 13 | g.32338661del | CA2739277586 | BRCA2 | c.4306del (p.Ile1436LeufsTer12) c.3937del (p.Ile1313LeufsTer12) n.4306del | ClinVar |
| 13 | g.32338661A= | CA2082810418 | BRCA2 | c.4306A= (p.Ile1436=) c.3937A= (p.Ile1313=) n.4306A= | |
| 13 | g.32338661A>C | CA387780749 | BRCA2 | c.4306A>C (p.Ile1436Leu) c.3937A>C (p.Ile1313Leu) n.4306A>C | |
| 13 | g.32338661A>G | CA6940768 | BRCA2 | c.4306A>G (p.Ile1436Val) c.3937A>G (p.Ile1313Val) n.4306A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338661A>T | CA387780748 | BRCA2 | c.4306A>T (p.Ile1436Phe) c.3937A>T (p.Ile1313Phe) n.4306A>T | |
| 13 | g.32338662T>A | CA387780756 | BRCA2 | c.4307T>A (p.Ile1436Asn) c.3938T>A (p.Ile1313Asn) n.4307T>A | dbSNP COSMIC COSMIC |
| 13 | g.32338662T>C | CA6940769 | BRCA2 | c.4307T>C (p.Ile1436Thr) c.3938T>C (p.Ile1313Thr) n.4307T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338662T>G | CA387780759 | BRCA2 | c.4307T>G (p.Ile1436Ser) c.3938T>G (p.Ile1313Ser) n.4307T>G | |
| 13 | g.32338662T= | CA2082810423 | BRCA2 | c.4307T= (p.Ile1436=) c.3938T= (p.Ile1313=) n.4307T= | |
| 13 | g.32338663T>A | CA483438178 | BRCA2 | c.4308T>A (p.Ile1436=) c.3939T>A (p.Ile1313=) n.4308T>A | ClinVar dbSNP |
| 13 | g.32338663T>C | CA483438176 | BRCA2 | c.4308T>C (p.Ile1436=) c.3939T>C (p.Ile1313=) n.4308T>C | |
| 13 | g.32338663T>G | CA387780762 | BRCA2 | c.4308T>G (p.Ile1436Met) c.3939T>G (p.Ile1313Met) n.4308T>G | |
| 13 | g.32338664A= | CA2082810431 | BRCA2 | c.4309A= (p.Ser1437=) c.3940A= (p.Ser1314=) n.4309A= | |
| 13 | g.32338664A>C | CA387780778 | BRCA2 | c.4309A>C (p.Ser1437Arg) c.3940A>C (p.Ser1314Arg) n.4309A>C | gnomAD v4 |
| 13 | g.32338664A>G | CA387780765 | BRCA2 | c.4309A>G (p.Ser1437Gly) c.3940A>G (p.Ser1314Gly) n.4309A>G | dbSNP gnomAD v4 |
| 13 | g.32338664A>T | CA387780774 | BRCA2 | c.4309A>T (p.Ser1437Cys) c.3940A>T (p.Ser1314Cys) n.4309A>T | ClinVar dbSNP |
| 13 | g.32338665G>A | CA387780780 | BRCA2 | c.4310G>A (p.Ser1437Asn) c.3941G>A (p.Ser1314Asn) n.4310G>A | ClinVar dbSNP |
| 13 | g.32338665G>C | CA387780781 | BRCA2 | c.4310G>C (p.Ser1437Thr) c.3941G>C (p.Ser1314Thr) n.4310G>C | ClinVar dbSNP |
| 13 | g.32338665G= | CA2082810444 | BRCA2 | c.4310G= (p.Ser1437=) c.3941G= (p.Ser1314=) n.4310G= | |
| 13 | g.32338665G>T | CA387780783 | BRCA2 | c.4310G>T (p.Ser1437Ile) c.3941G>T (p.Ser1314Ile) n.4310G>T | |
| 13 | g.32338667_32338668dup | CA16619705 | BRCA2 | c.4312_4313dup (p.Ala1439SerfsTer10) c.3943_3944dup (p.Ala1316SerfsTer10) n.4312_4313dup | ClinVar dbSNP |
| 13 | g.32338666T>A | CA387780785 | BRCA2 | c.4311T>A (p.Ser1437Arg) c.3942T>A (p.Ser1314Arg) n.4311T>A | dbSNP |
| 13 | g.32338666T>C | CA483438184 | BRCA2 | c.4311T>C (p.Ser1437=) c.3942T>C (p.Ser1314=) n.4311T>C | ClinVar dbSNP |
| 13 | g.32338666T>G | CA387780787 | BRCA2 | c.4311T>G (p.Ser1437Arg) c.3942T>G (p.Ser1314Arg) n.4311T>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338666T= | CA2082810453 | BRCA2 | c.4311T= (p.Ser1437=) c.3942T= (p.Ser1314=) n.4311T= | |
| 13 | g.32338667G>A | CA019946 | BRCA2 | c.4312G>A (p.Val1438Ile) c.3943G>A (p.Val1315Ile) n.4312G>A | ClinVar dbSNP |
| 13 | g.32338667G>C | CA387780792 | BRCA2 | c.4312G>C (p.Val1438Leu) c.3943G>C (p.Val1315Leu) n.4312G>C | dbSNP |
| 13 | g.32338667G= | CA2082810472 | BRCA2 | c.4312G= (p.Val1438=) c.3943G= (p.Val1315=) n.4312G= | |
| 13 | g.32338667G>T | CA387780790 | BRCA2 | c.4312G>T (p.Val1438Phe) c.3943G>T (p.Val1315Phe) n.4312G>T | |
| 13 | g.32338668T>A | CA387780793 | BRCA2 | c.4313T>A (p.Val1438Asp) c.3944T>A (p.Val1315Asp) n.4313T>A | dbSNP |
| 13 | g.32338668T>C | CA387780795 | BRCA2 | c.4313T>C (p.Val1438Ala) c.3944T>C (p.Val1315Ala) n.4313T>C | ClinVar dbSNP |
| 13 | g.32338668T>G | CA387780796 | BRCA2 | c.4313T>G (p.Val1438Gly) c.3944T>G (p.Val1315Gly) n.4313T>G | |
| 13 | g.32338668_32338669delinsTC | CA2082810480 | BRCA2 | c.4313_4314delinsTC (p.Val1438=) c.3944_3945delinsTC (p.Val1315=) n.4313_4314delinsTC | |
| 13 | g.32338669del | CA019954 | BRCA2 | c.4314del (p.Ala1439ProfsTer9) c.3945del (p.Ala1316ProfsTer9) n.4314del | ClinVar dbSNP |
| 13 | g.32338669C>A | CA483438185 | BRCA2 | c.4314C>A (p.Val1438=) c.3945C>A (p.Val1315=) n.4314C>A | dbSNP gnomAD v4 |
| 13 | g.32338669C= | CA2082810496 | BRCA2 | c.4314C= (p.Val1438=) c.3945C= (p.Val1315=) n.4314C= | |
| 13 | g.32338669C>G | CA483438186 | BRCA2 | c.4314C>G (p.Val1438=) c.3945C>G (p.Val1315=) n.4314C>G | dbSNP |
| 13 | g.32338669C>T | CA019951 | BRCA2 | c.4314C>T (p.Val1438=) c.3945C>T (p.Val1315=) n.4314C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 13 | g.32338670G>A | CA019960 | BRCA2 | c.4315G>A (p.Ala1439Thr) c.3946G>A (p.Ala1316Thr) n.4315G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 13 | g.32338670G>C | CA387780800 | BRCA2 | c.4315G>C (p.Ala1439Pro) c.3946G>C (p.Ala1316Pro) n.4315G>C | |
| 13 | g.32338670G= | CA2082810517 | BRCA2 | c.4315G= (p.Ala1439=) c.3946G= (p.Ala1316=) n.4315G= | |
| 13 | g.32338670G>T | CA387780802 | BRCA2 | c.4315G>T (p.Ala1439Ser) c.3946G>T (p.Ala1316Ser) n.4315G>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338671C>A | CA019966 | BRCA2 | c.4316C>A (p.Ala1439Asp) c.3947C>A (p.Ala1316Asp) n.4316C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338671C= | CA2082810534 | BRCA2 | c.4316C= (p.Ala1439=) c.3947C= (p.Ala1316=) n.4316C= | |
| 13 | g.32338671C>G | CA387780809 | BRCA2 | c.4316C>G (p.Ala1439Gly) c.3947C>G (p.Ala1316Gly) n.4316C>G | |
| 13 | g.32338671C>T | CA387780811 | BRCA2 | c.4316C>T (p.Ala1439Val) c.3947C>T (p.Ala1316Val) n.4316C>T | ClinVar dbSNP |
| 13 | g.32338671_32338682delinsCCAAAGAGTCAT | CA2082810533 | BRCA2 | c.4316_4327delinsCCAAAGAGTCAT (p.Ala1439=) c.3947_3958delinsCCAAAGAGTCAT (p.Ala1316=) n.4316_4327delinsCCAAAGAGTCAT | |
| 13 | g.32338672C>A | CA483438189 | BRCA2 | c.4317C>A (p.Ala1439=) c.3948C>A (p.Ala1316=) n.4317C>A | dbSNP gnomAD v4 |
| 13 | g.32338672C>G | CA483438191 | BRCA2 | c.4317C>G (p.Ala1439=) c.3948C>G (p.Ala1316=) n.4317C>G | dbSNP |
| 13 | g.32338672C>T | CA483438192 | BRCA2 | c.4317C>T (p.Ala1439=) c.3948C>T (p.Ala1316=) n.4317C>T | dbSNP COSMIC COSMIC |
| 13 | g.32338672_32338674delinsCAA | CA2082810551 | BRCA2 | c.4317_4319delinsCAA (p.Ala1439=) c.3948_3950delinsCAA (p.Ala1316=) n.4317_4319delinsCAA | |
| 13 | g.32338674_32338681del | CA2580087273 | BRCA2 | c.4319_4326del (p.Lys1440IlefsTer2) c.3950_3957del (p.Lys1317IlefsTer2) n.4319_4326del | ClinVar |
| 13 | g.32338672_32338682del | CA913188571 | BRCA2 | c.4317_4327del (p.Lys1440Ter) c.3948_3958del (p.Lys1317Ter) n.4317_4327del | ClinVar dbSNP |
| 13 | g.32338673A= | CA2082810576 | BRCA2 | c.4318A= (p.Lys1440=) c.3949A= (p.Lys1317=) n.4318A= | |
| 13 | g.32338673A>C | CA387780813 | BRCA2 | c.4318A>C (p.Lys1440Gln) c.3949A>C (p.Lys1317Gln) n.4318A>C | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338673A>G | CA019972 | BRCA2 | c.4318A>G (p.Lys1440Glu) c.3949A>G (p.Lys1317Glu) n.4318A>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338673A>T | CA387780815 | BRCA2 | c.4318A>T (p.Lys1440Ter) c.3949A>T (p.Lys1317Ter) n.4318A>T | ClinVar dbSNP |
| 13 | g.32338675del | CA2695218199 | BRCA2 | c.4320del (p.Glu1441SerfsTer7) c.3951del (p.Glu1318SerfsTer7) n.4320del | |
| 13 | g.32338674_32338675del | CA019975 | BRCA2 | c.4319_4320del (p.Lys1440ArgfsTer4) c.3950_3951del (p.Lys1317ArgfsTer4) n.4319_4320del | ClinVar dbSNP |
| 13 | g.32338674A= | CA2082810592 | BRCA2 | c.4319A= (p.Lys1440=) c.3950A= (p.Lys1317=) n.4319A= | |
| 13 | g.32338674A>C | CA387780816 | BRCA2 | c.4319A>C (p.Lys1440Thr) c.3950A>C (p.Lys1317Thr) n.4319A>C | |
| 13 | g.32338674A>G | CA019980 | BRCA2 | c.4319A>G (p.Lys1440Arg) c.3950A>G (p.Lys1317Arg) n.4319A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338674A>T | CA387780817 | BRCA2 | c.4319A>T (p.Lys1440Ile) c.3950A>T (p.Lys1317Ile) n.4319A>T | dbSNP |
| 13 | g.32338674_32338676delinsAAG | CA2082810600 | BRCA2 | c.4319_4321delinsAAG (p.Lys1440=) c.3950_3952delinsAAG (p.Lys1317=) n.4319_4321delinsAAG | |
| 13 | g.32338675A= | CA2082810617 | BRCA2 | c.4320A= (p.Lys1440=) c.3951A= (p.Lys1317=) n.4320A= | |
| 13 | g.32338675A>C | CA6940771 | BRCA2 | c.4320A>C (p.Lys1440Asn) c.3951A>C (p.Lys1317Asn) n.4320A>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338675A>G | CA6940770 | BRCA2 | c.4320A>G (p.Lys1440=) c.3951A>G (p.Lys1317=) n.4320A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338675A>T | CA387780819 | BRCA2 | c.4320A>T (p.Lys1440Asn) c.3951A>T (p.Lys1317Asn) n.4320A>T | |
| 13 | g.32338677_32338678del | CA915948461 | BRCA2 | c.4322_4323del (p.Glu1441ValfsTer3) c.3953_3954del (p.Glu1318ValfsTer3) n.4322_4323del | ClinVar dbSNP |
| 13 | g.32338676G>A | CA387780820 | BRCA2 | c.4321G>A (p.Glu1441Lys) c.3952G>A (p.Glu1318Lys) n.4321G>A | ClinVar dbSNP |
| 13 | g.32338676G>C | CA10579610 | BRCA2 | c.4321G>C (p.Glu1441Gln) c.3952G>C (p.Glu1318Gln) n.4321G>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338676G= | CA2082810641 | BRCA2 | c.4321G= (p.Glu1441=) c.3952G= (p.Glu1318=) n.4321G= | |
| 13 | g.32338676G>T | CA387780821 | BRCA2 | c.4321G>T (p.Glu1441Ter) c.3952G>T (p.Glu1318Ter) n.4321G>T | ClinVar dbSNP COSMIC COSMIC |
| 13 | g.32338677A= | CA2082810665 | BRCA2 | c.4322A= (p.Glu1441=) c.3953A= (p.Glu1318=) n.4322A= | |
| 13 | g.32338677A>C | CA387780824 | BRCA2 | c.4322A>C (p.Glu1441Ala) c.3953A>C (p.Glu1318Ala) n.4322A>C | ClinVar dbSNP |
| 13 | g.32338677A>G | CA387780825 | BRCA2 | c.4322A>G (p.Glu1441Gly) c.3953A>G (p.Glu1318Gly) n.4322A>G | ClinVar dbSNP |
| 13 | g.32338677A>T | CA387780826 | BRCA2 | c.4322A>T (p.Glu1441Val) c.3953A>T (p.Glu1318Val) n.4322A>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338678G>A | CA10579611 | BRCA2 | c.4323G>A (p.Glu1441=) c.3954G>A (p.Glu1318=) n.4323G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338678G>C | CA387780829 | BRCA2 | c.4323G>C (p.Glu1441Asp) c.3954G>C (p.Glu1318Asp) n.4323G>C | dbSNP |
| 13 | g.32338678G= | CA2082810677 | BRCA2 | c.4323G= (p.Glu1441=) c.3954G= (p.Glu1318=) n.4323G= | |
| 13 | g.32338678G>T | CA387780828 | BRCA2 | c.4323G>T (p.Glu1441Asp) c.3954G>T (p.Glu1318Asp) n.4323G>T | COSMIC COSMIC |
| 13 | g.32338679T>A | CA387780830 | BRCA2 | c.4324T>A (p.Ser1442Thr) c.3955T>A (p.Ser1319Thr) n.4324T>A | dbSNP |
| 13 | g.32338679T>C | CA387780831 | BRCA2 | c.4324T>C (p.Ser1442Pro) c.3955T>C (p.Ser1319Pro) n.4324T>C | dbSNP |
| 13 | g.32338679T>G | CA387780832 | BRCA2 | c.4324T>G (p.Ser1442Ala) c.3955T>G (p.Ser1319Ala) n.4324T>G | dbSNP gnomAD v4 |
| 13 | g.32338680C>A | CA019986 | BRCA2 | c.4325C>A (p.Ser1442Ter) c.3956C>A (p.Ser1319Ter) n.4325C>A | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
| 13 | g.32338680C= | CA2082810692 | BRCA2 | c.4325C= (p.Ser1442=) c.3956C= (p.Ser1319=) n.4325C= | |
| 13 | g.32338680C>G | CA019993 | BRCA2 | c.4325C>G (p.Ser1442Ter) c.3956C>G (p.Ser1319Ter) n.4325C>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338680C>T | CA387780833 | BRCA2 | c.4325C>T (p.Ser1442Leu) c.3956C>T (p.Ser1319Leu) n.4325C>T | ClinVar dbSNP |
| 13 | g.32338681A= | CA2082810707 | BRCA2 | c.4326A= (p.Ser1442=) c.3957A= (p.Ser1319=) n.4326A= | |
| 13 | g.32338681A>C | CA483438210 | BRCA2 | c.4326A>C (p.Ser1442=) c.3957A>C (p.Ser1319=) n.4326A>C | |
| 13 | g.32338681A>G | CA247507538 | BRCA2 | c.4326A>G (p.Ser1442=) c.3957A>G (p.Ser1319=) n.4326A>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338681A>T | CA483438209 | BRCA2 | c.4326A>T (p.Ser1442=) c.3957A>T (p.Ser1319=) n.4326A>T | |
| 13 | g.32338682T>A | CA387780836 | BRCA2 | c.4327T>A (p.Phe1443Ile) c.3958T>A (p.Phe1320Ile) n.4327T>A | dbSNP |
| 13 | g.32338682T>C | CA387780838 | BRCA2 | c.4327T>C (p.Phe1443Leu) c.3958T>C (p.Phe1320Leu) n.4327T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338682T>G | CA387780840 | BRCA2 | c.4327T>G (p.Phe1443Val) c.3958T>G (p.Phe1320Val) n.4327T>G | dbSNP |
| 13 | g.32338682T= | CA2082810717 | BRCA2 | c.4327T= (p.Phe1443=) c.3958T= (p.Phe1320=) n.4327T= | |
| 13 | g.32338684del | CA2695218200 | BRCA2 | c.4329del (p.Phe1443LeufsTer5) c.3960del (p.Phe1320LeufsTer5) n.4329del | |
| 13 | g.32338683T>A | CA387780847 | BRCA2 | c.4328T>A (p.Phe1443Tyr) c.3959T>A (p.Phe1320Tyr) n.4328T>A | dbSNP |
| 13 | g.32338683T>C | CA387780848 | BRCA2 | c.4328T>C (p.Phe1443Ser) c.3959T>C (p.Phe1320Ser) n.4328T>C | |
| 13 | g.32338683T>G | CA387780842 | BRCA2 | c.4328T>G (p.Phe1443Cys) c.3959T>G (p.Phe1320Cys) n.4328T>G | ClinVar |
| 13 | g.32338684T>A | CA387780850 | BRCA2 | c.4329T>A (p.Phe1443Leu) c.3960T>A (p.Phe1320Leu) n.4329T>A | dbSNP |
| 13 | g.32338684T>C | CA483438219 | BRCA2 | c.4329T>C (p.Phe1443=) c.3960T>C (p.Phe1320=) n.4329T>C | |
| 13 | g.32338684T>G | CA387780851 | BRCA2 | c.4329T>G (p.Phe1443Leu) c.3960T>G (p.Phe1320Leu) n.4329T>G | ClinVar |
| 13 | g.32338684_32338689delinsTAATAA | CA2082810726 | BRCA2 | c.4329_4334delinsTAATAA (p.Phe1443=) c.3960_3965delinsTAATAA (p.Phe1320=) n.4329_4334delinsTAATAA | |
| 13 | g.32338685A>C | CA387780853 | BRCA2 | c.4330A>C (p.Asn1444His) c.3961A>C (p.Asn1321His) n.4330A>C | |
| 13 | g.32338685A>G | CA387780854 | BRCA2 | c.4330A>G (p.Asn1444Asp) c.3961A>G (p.Asn1321Asp) n.4330A>G | |
| 13 | g.32338685A>T | CA387780855 | BRCA2 | c.4330A>T (p.Asn1444Tyr) c.3961A>T (p.Asn1321Tyr) n.4330A>T | dbSNP |
| 13 | g.32338688_32338692del | CA913190947 | BRCA2 | c.4333_4337del (p.Lys1445CysfsTer5) c.3964_3968del (p.Lys1322CysfsTer5) n.4333_4337del | ClinVar dbSNP |
| 13 | g.32338686A= | CA2082810733 | BRCA2 | c.4331A= (p.Asn1444=) c.3962A= (p.Asn1321=) n.4331A= | |
| 13 | g.32338686A>C | CA387780858 | BRCA2 | c.4331A>C (p.Asn1444Thr) c.3962A>C (p.Asn1321Thr) n.4331A>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338686A>G | CA019996 | BRCA2 | c.4331A>G (p.Asn1444Ser) c.3962A>G (p.Asn1321Ser) n.4331A>G | ClinVar dbSNP |
| 13 | g.32338686A>T | CA387780857 | BRCA2 | c.4331A>T (p.Asn1444Ile) c.3962A>T (p.Asn1321Ile) n.4331A>T | dbSNP |
| 13 | g.32338687T>A | CA387780860 | BRCA2 | c.4332T>A (p.Asn1444Lys) c.3963T>A (p.Asn1321Lys) n.4332T>A | |
| 13 | g.32338687T>C | CA483438228 | BRCA2 | c.4332T>C (p.Asn1444=) c.3963T>C (p.Asn1321=) n.4332T>C | gnomAD v4 |
| 13 | g.32338687T>G | CA387780861 | BRCA2 | c.4332T>G (p.Asn1444Lys) c.3963T>G (p.Asn1321Lys) n.4332T>G | |
| 13 | g.32338688A= | CA2082810748 | BRCA2 | c.4333A= (p.Lys1445=) c.3964A= (p.Lys1322=) n.4333A= | |
| 13 | g.32338688A>C | CA387780863 | BRCA2 | c.4333A>C (p.Lys1445Gln) c.3964A>C (p.Lys1322Gln) n.4333A>C | |
| 13 | g.32338688A>G | CA020001 | BRCA2 | c.4333A>G (p.Lys1445Glu) c.3964A>G (p.Lys1322Glu) n.4333A>G | ClinVar dbSNP |
| 13 | g.32338688A>T | CA387780864 | BRCA2 | c.4333A>T (p.Lys1445Ter) c.3964A>T (p.Lys1322Ter) n.4333A>T | dbSNP |
| 13 | g.32338688_32338693delinsAAAATT | CA2082810746 | BRCA2 | c.4333_4338delinsAAAATT (p.Lys1445=) c.3964_3969delinsAAAATT (p.Lys1322=) n.4333_4338delinsAAAATT | |
| 13 | g.32338689A= | CA2082810758 | BRCA2 | c.4334A= (p.Lys1445=) c.3965A= (p.Lys1322=) n.4334A= | |
| 13 | g.32338689A>C | CA387780866 | BRCA2 | c.4334A>C (p.Lys1445Thr) c.3965A>C (p.Lys1322Thr) n.4334A>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338689A>G | CA387780870 | BRCA2 | c.4334A>G (p.Lys1445Arg) c.3965A>G (p.Lys1322Arg) n.4334A>G | gnomAD v4 |
| 13 | g.32338689A>T | CA387780868 | BRCA2 | c.4334A>T (p.Lys1445Ile) c.3965A>T (p.Lys1322Ile) n.4334A>T | dbSNP |
| 13 | g.32338689_32338693del | CA10589253 | BRCA2 | c.4334_4338del (p.Lys1445SerfsTer5) c.3965_3969del (p.Lys1322SerfsTer5) n.4334_4338del | ClinVar dbSNP |
| 13 | g.32338690A= | CA2082810770 | BRCA2 | c.4335A= (p.Lys1445=) c.3966A= (p.Lys1322=) n.4335A= | |
| 13 | g.32338690A>C | CA16614301 | BRCA2 | c.4335A>C (p.Lys1445Asn) c.3966A>C (p.Lys1322Asn) n.4335A>C | ClinVar dbSNP |
| 13 | g.32338690A>G | CA483438235 | BRCA2 | c.4335A>G (p.Lys1445=) c.3966A>G (p.Lys1322=) n.4335A>G | |
| 13 | g.32338690A>T | CA387780871 | BRCA2 | c.4335A>T (p.Lys1445Asn) c.3966A>T (p.Lys1322Asn) n.4335A>T | gnomAD v4 |
| 13 | g.32338691A= | CA2082810784 | BRCA2 | c.4336A= (p.Ile1446=) c.3967A= (p.Ile1323=) n.4336A= | |
| 13 | g.32338691A>C | CA387780873 | BRCA2 | c.4336A>C (p.Ile1446Leu) c.3967A>C (p.Ile1323Leu) n.4336A>C | |
| 13 | g.32338691A>G | CA10577471 | BRCA2 | c.4336A>G (p.Ile1446Val) c.3967A>G (p.Ile1323Val) n.4336A>G | ClinVar dbSNP |
| 13 | g.32338691A>T | CA387780875 | BRCA2 | c.4336A>T (p.Ile1446Phe) c.3967A>T (p.Ile1323Phe) n.4336A>T | dbSNP |
| 13 | g.32338692T>A | CA387780877 | BRCA2 | c.4337T>A (p.Ile1446Asn) c.3968T>A (p.Ile1323Asn) n.4337T>A | dbSNP |
| 13 | g.32338692T>C | CA387780878 | BRCA2 | c.4337T>C (p.Ile1446Thr) c.3968T>C (p.Ile1323Thr) n.4337T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338692T>G | CA387780879 | BRCA2 | c.4337T>G (p.Ile1446Ser) c.3968T>G (p.Ile1323Ser) n.4337T>G | dbSNP |
| 13 | g.32338692T= | CA2082810792 | BRCA2 | c.4337T= (p.Ile1446=) c.3968T= (p.Ile1323=) n.4337T= | |
| 13 | g.32338693T>A | CA483438237 | BRCA2 | c.4338T>A (p.Ile1446=) c.3969T>A (p.Ile1323=) n.4338T>A | dbSNP |
| 13 | g.32338693T>C | CA348801 | BRCA2 | c.4338T>C (p.Ile1446=) c.3969T>C (p.Ile1323=) n.4338T>C | ClinVar dbSNP |
| 13 | g.32338693T>G | CA387780880 | BRCA2 | c.4338T>G (p.Ile1446Met) c.3969T>G (p.Ile1323Met) n.4338T>G | |
| 13 | g.32338693T= | CA2082810810 | BRCA2 | c.4338T= (p.Ile1446=) c.3969T= (p.Ile1323=) n.4338T= | |
| 13 | g.32338693_32338694delinsTG | CA2082810804 | BRCA2 | c.4338_4339delinsTG (p.Ile1446=) c.3969_3970delinsTG (p.Ile1323=) n.4338_4339delinsTG | |
| 13 | g.32338694del | CA020014 | BRCA2 | c.4339del (p.Val1447Ter) c.3970del (p.Val1324Ter) n.4339del | ClinVar dbSNP |
| 13 | g.32338694G>A | CA16619706 | BRCA2 | c.4339G>A (p.Val1447Ile) c.3970G>A (p.Val1324Ile) n.4339G>A | ClinVar dbSNP |
| 13 | g.32338694G>C | CA387780883 | BRCA2 | c.4339G>C (p.Val1447Leu) c.3970G>C (p.Val1324Leu) n.4339G>C | dbSNP |
| 13 | g.32338694G= | CA2082810824 | BRCA2 | c.4339G= (p.Val1447=) c.3970G= (p.Val1324=) n.4339G= | |
| 13 | g.32338694G>T | CA387780881 | BRCA2 | c.4339G>T (p.Val1447Leu) c.3970G>T (p.Val1324Leu) n.4339G>T | ClinVar |
| 13 | g.32338695T>A | CA387780885 | BRCA2 | c.4340T>A (p.Val1447Glu) c.3971T>A (p.Val1324Glu) n.4340T>A | |
| 13 | g.32338695T>C | CA387780887 | BRCA2 | c.4340T>C (p.Val1447Ala) c.3971T>C (p.Val1324Ala) n.4340T>C | ClinVar dbSNP |
| 13 | g.32338695T>G | CA387780888 | BRCA2 | c.4340T>G (p.Val1447Gly) c.3971T>G (p.Val1324Gly) n.4340T>G | |
| 13 | g.32338695T= | CA2082810830 | BRCA2 | c.4340T= (p.Val1447=) c.3971T= (p.Val1324=) n.4340T= | |
| 13 | g.32338696A>C | CA483438241 | BRCA2 | c.4341A>C (p.Val1447=) c.3972A>C (p.Val1324=) n.4341A>C | |
| 13 | g.32338696A>G | CA483438242 | BRCA2 | c.4341A>G (p.Val1447=) c.3972A>G (p.Val1324=) n.4341A>G | ClinVar dbSNP |
| 13 | g.32338696A>T | CA483438243 | BRCA2 | c.4341A>T (p.Val1447=) c.3972A>T (p.Val1324=) n.4341A>T | dbSNP |
| 13 | g.32338697_32338698del | CA2499222163 | BRCA2 | c.4342_4343del (p.Asn1448PhefsTer3) c.3973_3974del (p.Asn1325PhefsTer3) n.4342_4343del | ClinVar |
| 13 | g.32338697A>C | CA387780889 | BRCA2 | c.4342A>C (p.Asn1448His) c.3973A>C (p.Asn1325His) n.4342A>C | |
| 13 | g.32338697A>G | CA387780891 | BRCA2 | c.4342A>G (p.Asn1448Asp) c.3973A>G (p.Asn1325Asp) n.4342A>G | |
| 13 | g.32338697A>T | CA387780892 | BRCA2 | c.4342A>T (p.Asn1448Tyr) c.3973A>T (p.Asn1325Tyr) n.4342A>T | dbSNP |
| 13 | g.32338698A= | CA2082810838 | BRCA2 | c.4343A= (p.Asn1448=) c.3974A= (p.Asn1325=) n.4343A= | |
| 13 | g.32338698A>C | CA387780896 | BRCA2 | c.4343A>C (p.Asn1448Thr) c.3974A>C (p.Asn1325Thr) n.4343A>C | |
| 13 | g.32338698A>G | CA387780894 | BRCA2 | c.4343A>G (p.Asn1448Ser) c.3974A>G (p.Asn1325Ser) n.4343A>G | |
| 13 | g.32338698A>T | CA6940772 | BRCA2 | c.4343A>T (p.Asn1448Ile) c.3974A>T (p.Asn1325Ile) n.4343A>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338698_32338703delinsATTTCT | CA2082810852 | BRCA2 | c.4343_4348delinsATTTCT (p.Asn1448=) c.3974_3979delinsATTTCT (p.Asn1325=) n.4343_4348delinsATTTCT | |
| 13 | g.32338699T>A | CA387780897 | BRCA2 | c.4344T>A (p.Asn1448Lys) c.3975T>A (p.Asn1325Lys) n.4344T>A | dbSNP |
| 13 | g.32338699T>C | CA483438246 | BRCA2 | c.4344T>C (p.Asn1448=) c.3975T>C (p.Asn1325=) n.4344T>C | ClinVar gnomAD v4 |
| 13 | g.32338699T>G | CA16619707 | BRCA2 | c.4344T>G (p.Asn1448Lys) c.3975T>G (p.Asn1325Lys) n.4344T>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338699T= | CA2082810863 | BRCA2 | c.4344T= (p.Asn1448=) c.3975T= (p.Asn1325=) n.4344T= | |
| 13 | g.32338700_32338701dup | CA891842167 | BRCA2 | c.4345_4346dup (p.Phe1450SerfsTer14) c.3976_3977dup (p.Phe1327SerfsTer14) n.4345_4346dup | |
| 13 | g.32338701_32338705del | CA645509346 | BRCA2 | c.4346_4350del (p.Phe1449Ter) c.3977_3981del (p.Phe1326Ter) n.4346_4350del | ClinVar dbSNP |
| 13 | g.32338700T>A | CA387780900 | BRCA2 | c.4345T>A (p.Phe1449Ile) c.3976T>A (p.Phe1326Ile) n.4345T>A | |
| 13 | g.32338700T>C | CA387780901 | BRCA2 | c.4345T>C (p.Phe1449Leu) c.3976T>C (p.Phe1326Leu) n.4345T>C | |
| 13 | g.32338700T>G | CA387780903 | BRCA2 | c.4345T>G (p.Phe1449Val) c.3976T>G (p.Phe1326Val) n.4345T>G | dbSNP |
| 13 | g.32338701T>A | CA387780905 | BRCA2 | c.4346T>A (p.Phe1449Tyr) c.3977T>A (p.Phe1326Tyr) n.4346T>A | ClinVar dbSNP |
| 13 | g.32338701T>C | CA387780908 | BRCA2 | c.4346T>C (p.Phe1449Ser) c.3977T>C (p.Phe1326Ser) n.4346T>C | ClinVar |
| 13 | g.32338701T>G | CA387780907 | BRCA2 | c.4346T>G (p.Phe1449Cys) c.3977T>G (p.Phe1326Cys) n.4346T>G | |
| 13 | g.32338702C>A | CA16614149 | BRCA2 | c.4347C>A (p.Phe1449Leu) c.3978C>A (p.Phe1326Leu) n.4347C>A | ClinVar dbSNP |
| 13 | g.32338702C= | CA2082810872 | BRCA2 | c.4347C= (p.Phe1449=) c.3978C= (p.Phe1326=) n.4347C= | |
| 13 | g.32338702C>G | CA387780909 | BRCA2 | c.4347C>G (p.Phe1449Leu) c.3978C>G (p.Phe1326Leu) n.4347C>G | dbSNP |
| 13 | g.32338702C>T | CA483438252 | BRCA2 | c.4347C>T (p.Phe1449=) c.3978C>T (p.Phe1326=) n.4347C>T | dbSNP |
| 13 | g.32338703T>A | CA387780912 | BRCA2 | c.4348T>A (p.Phe1450Ile) c.3979T>A (p.Phe1327Ile) n.4348T>A | dbSNP |
| 13 | g.32338703T>C | CA387780913 | BRCA2 | c.4348T>C (p.Phe1450Leu) c.3979T>C (p.Phe1327Leu) n.4348T>C | |
| 13 | g.32338703T>G | CA387780919 | BRCA2 | c.4348T>G (p.Phe1450Val) c.3979T>G (p.Phe1327Val) n.4348T>G | |
| 13 | g.32338705dup | CA2580087275 | BRCA2 | c.4350dup (p.Asp1451Ter) c.3981dup (p.Asp1328Ter) n.4350dup | ClinVar |
| 13 | g.32338704T>A | CA387780921 | BRCA2 | c.4349T>A (p.Phe1450Tyr) c.3980T>A (p.Phe1327Tyr) n.4349T>A | dbSNP |
| 13 | g.32338704T>C | CA020021 | BRCA2 | c.4349T>C (p.Phe1450Ser) c.3980T>C (p.Phe1327Ser) n.4349T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338704T>G | CA387780924 | BRCA2 | c.4349T>G (p.Phe1450Cys) c.3980T>G (p.Phe1327Cys) n.4349T>G | |
| 13 | g.32338704T= | CA2082810885 | BRCA2 | c.4349T= (p.Phe1450=) c.3980T= (p.Phe1327=) n.4349T= | |
| 13 | g.32338705T>A | CA387780926 | BRCA2 | c.4350T>A (p.Phe1450Leu) c.3981T>A (p.Phe1327Leu) n.4350T>A | dbSNP |
| 13 | g.32338705T>C | CA483438254 | BRCA2 | c.4350T>C (p.Phe1450=) c.3981T>C (p.Phe1327=) n.4350T>C | COSMIC COSMIC |
| 13 | g.32338705T>G | CA387780927 | BRCA2 | c.4350T>G (p.Phe1450Leu) c.3981T>G (p.Phe1327Leu) n.4350T>G | |
| 13 | g.32338706G>A | CA387780929 | BRCA2 | c.4351G>A (p.Asp1451Asn) c.3982G>A (p.Asp1328Asn) n.4351G>A | ClinVar dbSNP |
| 13 | g.32338706G>C | CA387780930 | BRCA2 | c.4351G>C (p.Asp1451His) c.3982G>C (p.Asp1328His) n.4351G>C | dbSNP |
| 13 | g.32338706G= | CA2082810898 | BRCA2 | c.4351G= (p.Asp1451=) c.3982G= (p.Asp1328=) n.4351G= | |
| 13 | g.32338706G>T | CA387780933 | BRCA2 | c.4351G>T (p.Asp1451Tyr) c.3982G>T (p.Asp1328Tyr) n.4351G>T | dbSNP gnomAD v4 |
| 13 | g.32338706_32338713delinsGATCAGAA | CA2082810897 | BRCA2 | c.4351_4358delinsGATCAGAA (p.Asp1451=) c.3982_3989delinsGATCAGAA (p.Asp1328=) n.4351_4358delinsGATCAGAA | |
| 13 | g.32338707A= | CA2082810910 | BRCA2 | c.4352A= (p.Asp1451=) c.3983A= (p.Asp1328=) n.4352A= | |
| 13 | g.32338707A>C | CA387780936 | BRCA2 | c.4352A>C (p.Asp1451Ala) c.3983A>C (p.Asp1328Ala) n.4352A>C | ClinVar |
| 13 | g.32338707A>G | CA020025 | BRCA2 | c.4352A>G (p.Asp1451Gly) c.3983A>G (p.Asp1328Gly) n.4352A>G | ClinVar dbSNP |
| 13 | g.32338707A>T | CA387780934 | BRCA2 | c.4352A>T (p.Asp1451Val) c.3983A>T (p.Asp1328Val) n.4352A>T | ClinVar dbSNP |
| 13 | g.32338708_32338714del | CA658823579 | BRCA2 | c.4353_4359del (p.Pro1454AsnfsTer7) c.3984_3990del (p.Pro1331AsnfsTer7) n.4353_4359del | ClinVar dbSNP |
| 13 | g.32338708T>A | CA387780940 | BRCA2 | c.4353T>A (p.Asp1451Glu) c.3984T>A (p.Asp1328Glu) n.4353T>A | dbSNP |
| 13 | g.32338708T>C | CA483438258 | BRCA2 | c.4353T>C (p.Asp1451=) c.3984T>C (p.Asp1328=) n.4353T>C | ClinVar dbSNP |
| 13 | g.32338708T>G | CA387780938 | BRCA2 | c.4353T>G (p.Asp1451Glu) c.3984T>G (p.Asp1328Glu) n.4353T>G | ClinVar dbSNP |
| 13 | g.32338708T= | CA2082810925 | BRCA2 | c.4353T= (p.Asp1451=) c.3984T= (p.Asp1328=) n.4353T= | |
| 13 | g.32338709C>A | CA387780943 | BRCA2 | c.4354C>A (p.Gln1452Lys) c.3985C>A (p.Gln1329Lys) n.4354C>A | dbSNP |
| 13 | g.32338709C= | CA2082810939 | BRCA2 | c.4354C= (p.Gln1452=) c.3985C= (p.Gln1329=) n.4354C= | |
| 13 | g.32338709C>G | CA020031 | BRCA2 | c.4354C>G (p.Gln1452Glu) c.3985C>G (p.Gln1329Glu) n.4354C>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338709C>T | CA16606424 | BRCA2 | c.4354C>T (p.Gln1452Ter) c.3985C>T (p.Gln1329Ter) n.4354C>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338710A= | CA2082810948 | BRCA2 | c.4355A= (p.Gln1452=) c.3986A= (p.Gln1329=) n.4355A= | |
| 13 | g.32338710A>C | CA387780945 | BRCA2 | c.4355A>C (p.Gln1452Pro) c.3986A>C (p.Gln1329Pro) n.4355A>C | |
| 13 | g.32338710A>G | CA10579612 | BRCA2 | c.4355A>G (p.Gln1452Arg) c.3986A>G (p.Gln1329Arg) n.4355A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338710A>T | CA387780948 | BRCA2 | c.4355A>T (p.Gln1452Leu) c.3986A>T (p.Gln1329Leu) n.4355A>T | dbSNP |
| 13 | g.32338711G>A | CA483438261 | BRCA2 | c.4356G>A (p.Gln1452=) c.3987G>A (p.Gln1329=) n.4356G>A | dbSNP gnomAD v4 |
| 13 | g.32338711G>C | CA387780949 | BRCA2 | c.4356G>C (p.Gln1452His) c.3987G>C (p.Gln1329His) n.4356G>C | dbSNP |
| 13 | g.32338711G>T | CA387780950 | BRCA2 | c.4356G>T (p.Gln1452His) c.3987G>T (p.Gln1329His) n.4356G>T | |
| 13 | g.32338712A= | CA2082810957 | BRCA2 | c.4357A= (p.Lys1453=) c.3988A= (p.Lys1330=) n.4357A= | |
| 13 | g.32338712A>C | CA387780951 | BRCA2 | c.4357A>C (p.Lys1453Gln) c.3988A>C (p.Lys1330Gln) n.4357A>C | |
| 13 | g.32338712A>G | CA020036 | BRCA2 | c.4357A>G (p.Lys1453Glu) c.3988A>G (p.Lys1330Glu) n.4357A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338712A>T | CA387780952 | BRCA2 | c.4357A>T (p.Lys1453Ter) c.3988A>T (p.Lys1330Ter) n.4357A>T | dbSNP COSMIC COSMIC |
| 13 | g.32338713A= | CA2082810967 | BRCA2 | c.4358A= (p.Lys1453=) c.3989A= (p.Lys1330=) n.4358A= | |
| 13 | g.32338713A>C | CA387780954 | BRCA2 | c.4358A>C (p.Lys1453Thr) c.3989A>C (p.Lys1330Thr) n.4358A>C | ClinVar |
| 13 | g.32338713A>G | CA387780955 | BRCA2 | c.4358A>G (p.Lys1453Arg) c.3989A>G (p.Lys1330Arg) n.4358A>G | ClinVar dbSNP |
| 13 | g.32338713A>T | CA387780957 | BRCA2 | c.4358A>T (p.Lys1453Ile) c.3989A>T (p.Lys1330Ile) n.4358A>T | dbSNP |
| 13 | g.32338714A= | CA2082810976 | BRCA2 | c.4359A= (p.Lys1453=) c.3990A= (p.Lys1330=) n.4359A= | |
| 13 | g.32338714A>C | CA387780962 | BRCA2 | c.4359A>C (p.Lys1453Asn) c.3990A>C (p.Lys1330Asn) n.4359A>C | |
| 13 | g.32338714A>G | CA6940773 | BRCA2 | c.4359A>G (p.Lys1453=) c.3990A>G (p.Lys1330=) n.4359A>G | ClinVar dbSNP ExAC gnomAD v2 |
| 13 | g.32338714A>T | CA387780960 | BRCA2 | c.4359A>T (p.Lys1453Asn) c.3990A>T (p.Lys1330Asn) n.4359A>T | ClinVar dbSNP |
| 13 | g.32338714_32338715delinsAC | CA2082810972 | BRCA2 | c.4359_4360delinsAC (p.Lys1453=) c.3990_3991delinsAC (p.Lys1330=) n.4359_4360delinsAC | |
| 13 | g.32338715C>A | CA387780965 | BRCA2 | c.4360C>A (p.Pro1454Thr) c.3991C>A (p.Pro1331Thr) n.4360C>A | dbSNP |
| 13 | g.32338715C= | CA2082810985 | BRCA2 | c.4360C= (p.Pro1454=) c.3991C= (p.Pro1331=) n.4360C= | |
| 13 | g.32338715C>G | CA387780966 | BRCA2 | c.4360C>G (p.Pro1454Ala) c.3991C>G (p.Pro1331Ala) n.4360C>G | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338715C>T | CA387780968 | BRCA2 | c.4360C>T (p.Pro1454Ser) c.3991C>T (p.Pro1331Ser) n.4360C>T | ClinVar dbSNP |
| 13 | g.32338716del | CA915948462 | BRCA2 | c.4361del (p.Pro1454GlnfsTer9) c.3992del (p.Pro1331GlnfsTer9) n.4361del | ClinVar dbSNP |
| 13 | g.32338716C>A | CA387780970 | BRCA2 | c.4361C>A (p.Pro1454Gln) c.3992C>A (p.Pro1331Gln) n.4361C>A | dbSNP |
| 13 | g.32338716C= | CA2082810995 | BRCA2 | c.4361C= (p.Pro1454=) c.3992C= (p.Pro1331=) n.4361C= | |
| 13 | g.32338716C>G | CA6940774 | BRCA2 | c.4361C>G (p.Pro1454Arg) c.3992C>G (p.Pro1331Arg) n.4361C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338716C>T | CA6940775 | BRCA2 | c.4361C>T (p.Pro1454Leu) c.3992C>T (p.Pro1331Leu) n.4361C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338716_32338719del | CA1139770856 | BRCA2 | c.4361_4364del (p.Pro1454GlnfsTer8) c.3992_3995del (p.Pro1331GlnfsTer8) n.4361_4364del | |
| 13 | g.32338716_32338723delinsTCAGAT | CA2580087277 | BRCA2 | c.4361_4368delinsTCAGAT (p.Pro1454LeufsTer5) c.3992_3999delinsTCAGAT (p.Pro1331LeufsTer5) n.4361_4368delinsTCAGAT | ClinVar |
| 13 | g.32338717A= | CA2082811004 | BRCA2 | c.4362A= (p.Pro1454=) c.3993A= (p.Pro1331=) n.4362A= | |
| 13 | g.32338717A>C | CA483438269 | BRCA2 | c.4362A>C (p.Pro1454=) c.3993A>C (p.Pro1331=) n.4362A>C | dbSNP |
| 13 | g.32338717A>G | CA483438271 | BRCA2 | c.4362A>G (p.Pro1454=) c.3993A>G (p.Pro1331=) n.4362A>G | ClinVar dbSNP |
| 13 | g.32338717A>T | CA483438270 | BRCA2 | c.4362A>T (p.Pro1454=) c.3993A>T (p.Pro1331=) n.4362A>T | dbSNP |
| 13 | g.32338718G>A | CA387780974 | BRCA2 | c.4363G>A (p.Glu1455Lys) c.3994G>A (p.Glu1332Lys) n.4363G>A | dbSNP |
| 13 | g.32338718G>C | CA387780976 | BRCA2 | c.4363G>C (p.Glu1455Gln) c.3994G>C (p.Glu1332Gln) n.4363G>C | dbSNP |
| 13 | g.32338718G= | CA2082811010 | BRCA2 | c.4363G= (p.Glu1455=) c.3994G= (p.Glu1332=) n.4363G= | |
| 13 | g.32338718G>T | CA387780978 | BRCA2 | c.4363G>T (p.Glu1455Ter) c.3994G>T (p.Glu1332Ter) n.4363G>T | ClinVar dbSNP |
| 13 | g.32338719A= | CA2082811019 | BRCA2 | c.4364A= (p.Glu1455=) c.3995A= (p.Glu1332=) n.4364A= | |
| 13 | g.32338719A>C | CA387780979 | BRCA2 | c.4364A>C (p.Glu1455Ala) c.3995A>C (p.Glu1332Ala) n.4364A>C | |
| 13 | g.32338719A>G | CA387780981 | BRCA2 | c.4364A>G (p.Glu1455Gly) c.3995A>G (p.Glu1332Gly) n.4364A>G | |
| 13 | g.32338719A>T | CA387780982 | BRCA2 | c.4364A>T (p.Glu1455Val) c.3995A>T (p.Glu1332Val) n.4364A>T | ClinVar dbSNP |
| 13 | g.32338720del | CA2499222164 | BRCA2 | c.4365del (p.Glu1456AsnfsTer7) c.3996del (p.Glu1333AsnfsTer7) n.4365del | ClinVar dbSNP |
| 13 | g.32338720A= | CA2082811025 | BRCA2 | c.4365A= (p.Glu1455=) c.3996A= (p.Glu1332=) n.4365A= | |
| 13 | g.32338720A>C | CA387780986 | BRCA2 | c.4365A>C (p.Glu1455Asp) c.3996A>C (p.Glu1332Asp) n.4365A>C | |
| 13 | g.32338720A>G | CA483438273 | BRCA2 | c.4365A>G (p.Glu1455=) c.3996A>G (p.Glu1332=) n.4365A>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338720A>T | CA387780984 | BRCA2 | c.4365A>T (p.Glu1455Asp) c.3996A>T (p.Glu1332Asp) n.4365A>T | dbSNP |
| 13 | g.32338721G>A | CA10579613 | BRCA2 | c.4366G>A (p.Glu1456Lys) c.3997G>A (p.Glu1333Lys) n.4366G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338721G>C | CA387780989 | BRCA2 | c.4366G>C (p.Glu1456Gln) c.3997G>C (p.Glu1333Gln) n.4366G>C | dbSNP |
| 13 | g.32338721G= | CA2082811036 | BRCA2 | c.4366G= (p.Glu1456=) c.3997G= (p.Glu1333=) n.4366G= | |
| 13 | g.32338721G>T | CA10589254 | BRCA2 | c.4366G>T (p.Glu1456Ter) c.3997G>T (p.Glu1333Ter) n.4366G>T | ClinVar dbSNP |
| 13 | g.32338722A= | CA2082811060 | BRCA2 | c.4367A= (p.Glu1456=) c.3998A= (p.Glu1333=) n.4367A= | |
| 13 | g.32338722A>C | CA10583105 | BRCA2 | c.4367A>C (p.Glu1456Ala) c.3998A>C (p.Glu1333Ala) n.4367A>C | ClinVar dbSNP |
| 13 | g.32338722A>G | CA387780990 | BRCA2 | c.4367A>G (p.Glu1456Gly) c.3998A>G (p.Glu1333Gly) n.4367A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338722A>T | CA387780991 | BRCA2 | c.4367A>T (p.Glu1456Val) c.3998A>T (p.Glu1333Val) n.4367A>T | dbSNP |
| 13 | g.32338723A= | CA2082811072 | BRCA2 | c.4368A= (p.Glu1456=) c.3999A= (p.Glu1333=) n.4368A= | |
| 13 | g.32338723A>C | CA387780992 | BRCA2 | c.4368A>C (p.Glu1456Asp) c.3999A>C (p.Glu1333Asp) n.4368A>C | |
| 13 | g.32338723A>G | CA483438275 | BRCA2 | c.4368A>G (p.Glu1456=) c.3999A>G (p.Glu1333=) n.4368A>G | ClinVar dbSNP |
| 13 | g.32338723A>T | CA387780993 | BRCA2 | c.4368A>T (p.Glu1456Asp) c.3999A>T (p.Glu1333Asp) n.4368A>T | ClinVar dbSNP |
| 13 | g.32338724T>A | CA387780994 | BRCA2 | c.4369T>A (p.Leu1457Met) c.4000T>A (p.Leu1334Met) n.4369T>A | dbSNP |
| 13 | g.32338724T>C | CA020040 | BRCA2 | c.4369T>C (p.Leu1457=) c.4000T>C (p.Leu1334=) n.4369T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338724T>G | CA387780996 | BRCA2 | c.4369T>G (p.Leu1457Val) c.4000T>G (p.Leu1334Val) n.4369T>G | dbSNP |
| 13 | g.32338724T= | CA2082811081 | BRCA2 | c.4369T= (p.Leu1457=) c.4000T= (p.Leu1334=) n.4369T= | |
| 13 | g.32338725del | CA2825002139 | BRCA2 | c.4370del (p.Leu1457CysfsTer6) c.4001del (p.Leu1334CysfsTer6) n.4370del | ClinVar |
| 13 | g.32338725T>A | CA387780998 | BRCA2 | c.4370T>A (p.Leu1457Ter) c.4001T>A (p.Leu1334Ter) n.4370T>A | dbSNP |
| 13 | g.32338725T>C | CA387780999 | BRCA2 | c.4370T>C (p.Leu1457Ser) c.4001T>C (p.Leu1334Ser) n.4370T>C | dbSNP COSMIC COSMIC |
| 13 | g.32338725T>G | CA387781001 | BRCA2 | c.4370T>G (p.Leu1457Trp) c.4001T>G (p.Leu1334Trp) n.4370T>G | |
| 13 | g.32338726G>A | CA020045 | BRCA2 | c.4371G>A (p.Leu1457=) c.4002G>A (p.Leu1334=) n.4371G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338726G>C | CA387781006 | BRCA2 | c.4371G>C (p.Leu1457Phe) c.4002G>C (p.Leu1334Phe) n.4371G>C | dbSNP gnomAD v4 |
| 13 | g.32338726G= | CA2082811096 | BRCA2 | c.4371G= (p.Leu1457=) c.4002G= (p.Leu1334=) n.4371G= | |
| 13 | g.32338726G>T | CA387781004 | BRCA2 | c.4371G>T (p.Leu1457Phe) c.4002G>T (p.Leu1334Phe) n.4371G>T | ClinVar dbSNP |
| 13 | g.32338727del | CA2573149378 | BRCA2 | c.4372del (p.His1458IlefsTer5) c.4003del (p.His1335IlefsTer5) n.4372del | ClinVar dbSNP |
| 13 | g.32338727C>A | CA387781008 | BRCA2 | c.4372C>A (p.His1458Asn) c.4003C>A (p.His1335Asn) n.4372C>A | ClinVar |
| 13 | g.32338727C= | CA2082811106 | BRCA2 | c.4372C= (p.His1458=) c.4003C= (p.His1335=) n.4372C= | |
| 13 | g.32338727C>G | CA387781010 | BRCA2 | c.4372C>G (p.His1458Asp) c.4003C>G (p.His1335Asp) n.4372C>G | ClinVar |
| 13 | g.32338727C>T | CA020050 | BRCA2 | c.4372C>T (p.His1458Tyr) c.4003C>T (p.His1335Tyr) n.4372C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338728A= | CA2082811111 | BRCA2 | c.4373A= (p.His1458=) c.4004A= (p.His1335=) n.4373A= | |
| 13 | g.32338728A>C | CA387781012 | BRCA2 | c.4373A>C (p.His1458Pro) c.4004A>C (p.His1335Pro) n.4373A>C | |
| 13 | g.32338728A>G | CA020055 | BRCA2 | c.4373A>G (p.His1458Arg) c.4004A>G (p.His1335Arg) n.4373A>G | ClinVar dbSNP gnomAD v2 |
| 13 | g.32338728A>T | CA387781014 | BRCA2 | c.4373A>T (p.His1458Leu) c.4004A>T (p.His1335Leu) n.4373A>T | dbSNP |
| 13 | g.32338729T>A | CA387781016 | BRCA2 | c.4374T>A (p.His1458Gln) c.4005T>A (p.His1335Gln) n.4374T>A | ClinVar dbSNP |
| 13 | g.32338729T>C | CA16614302 | BRCA2 | c.4374T>C (p.His1458=) c.4005T>C (p.His1335=) n.4374T>C | ClinVar dbSNP |
| 13 | g.32338729T>G | CA387781018 | BRCA2 | c.4374T>G (p.His1458Gln) c.4005T>G (p.His1335Gln) n.4374T>G | |
| 13 | g.32338729T= | CA2082811127 | BRCA2 | c.4374T= (p.His1458=) c.4005T= (p.His1335=) n.4374T= | |
| 13 | g.32338729_32338730delinsTA | CA2082811134 | BRCA2 | c.4374_4375delinsTA (p.His1458=) c.4005_4006delinsTA (p.His1335=) n.4374_4375delinsTA | |
| 13 | g.32338730A= | CA2082811150 | BRCA2 | c.4375A= (p.Asn1459=) c.4006A= (p.Asn1336=) n.4375A= | |
| 13 | g.32338730A>C | CA387781019 | BRCA2 | c.4375A>C (p.Asn1459His) c.4006A>C (p.Asn1336His) n.4375A>C | gnomAD v4 |
| 13 | g.32338730A>G | CA387781021 | BRCA2 | c.4375A>G (p.Asn1459Asp) c.4006A>G (p.Asn1336Asp) n.4375A>G | |
| 13 | g.32338730A>T | CA387781023 | BRCA2 | c.4375A>T (p.Asn1459Tyr) c.4006A>T (p.Asn1336Tyr) n.4375A>T | ClinVar dbSNP |
| 13 | g.32338731dup | CA1139663199 | BRCA2 | c.4376dup (p.Asn1459LysfsTer7) c.4007dup (p.Asn1336LysfsTer7) n.4376dup | ClinVar dbSNP |
| 13 | g.32338731del | CA645509347 | BRCA2 | c.4376del (p.Asn1459ThrfsTer4) c.4007del (p.Asn1336ThrfsTer4) n.4376del | ClinVar dbSNP |
| 13 | g.32338731A= | CA2082811158 | BRCA2 | c.4376A= (p.Asn1459=) c.4007A= (p.Asn1336=) n.4376A= | |
| 13 | g.32338731A>C | CA387781025 | BRCA2 | c.4376A>C (p.Asn1459Thr) c.4007A>C (p.Asn1336Thr) n.4376A>C | |
| 13 | g.32338731A>G | CA020060 | BRCA2 | c.4376A>G (p.Asn1459Ser) c.4007A>G (p.Asn1336Ser) n.4376A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338731A>T | CA387781027 | BRCA2 | c.4376A>T (p.Asn1459Ile) c.4007A>T (p.Asn1336Ile) n.4376A>T | dbSNP |
| 13 | g.32338732C>A | CA387781029 | BRCA2 | c.4377C>A (p.Asn1459Lys) c.4008C>A (p.Asn1336Lys) n.4377C>A | |
| 13 | g.32338732C= | CA2082811167 | BRCA2 | c.4377C= (p.Asn1459=) c.4008C= (p.Asn1336=) n.4377C= | |
| 13 | g.32338732C>G | CA020067 | BRCA2 | c.4377C>G (p.Asn1459Lys) c.4008C>G (p.Asn1336Lys) n.4377C>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338732C>T | CA483438284 | BRCA2 | c.4377C>T (p.Asn1459=) c.4008C>T (p.Asn1336=) n.4377C>T | |
| 13 | g.32338732_32338734delinsCTT | CA2082811171 | BRCA2 | c.4377_4379delinsCTT (p.Asn1459=) c.4008_4010delinsCTT (p.Asn1336=) n.4377_4379delinsCTT | |
| 13 | g.32338733T>A | CA387781039 | BRCA2 | c.4378T>A (p.Phe1460Ile) c.4009T>A (p.Phe1337Ile) n.4378T>A | dbSNP |
| 13 | g.32338733T>C | CA387781035 | BRCA2 | c.4378T>C (p.Phe1460Leu) c.4009T>C (p.Phe1337Leu) n.4378T>C | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338733T>G | CA387781034 | BRCA2 | c.4378T>G (p.Phe1460Val) c.4009T>G (p.Phe1337Val) n.4378T>G | ClinVar dbSNP |
| 13 | g.32338733T= | CA2082811199 | BRCA2 | c.4378T= (p.Phe1460=) c.4009T= (p.Phe1337=) n.4378T= | |
| 13 | g.32338735_32338736del | CA020074 | BRCA2 | c.4380_4381del (p.Ser1461LeufsTer4) c.4011_4012del (p.Ser1338LeufsTer4) n.4380_4381del | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338734T>A | CA387781042 | BRCA2 | c.4379T>A (p.Phe1460Tyr) c.4010T>A (p.Phe1337Tyr) n.4379T>A | |
| 13 | g.32338734T>C | CA387781046 | BRCA2 | c.4379T>C (p.Phe1460Ser) c.4010T>C (p.Phe1337Ser) n.4379T>C | ClinVar dbSNP |
| 13 | g.32338734T>G | CA387781047 | BRCA2 | c.4379T>G (p.Phe1460Cys) c.4010T>G (p.Phe1337Cys) n.4379T>G | |
| 13 | g.32338734T= | CA2082811212 | BRCA2 | c.4379T= (p.Phe1460=) c.4010T= (p.Phe1337=) n.4379T= | |
| 13 | g.32338735T>A | CA387781049 | BRCA2 | c.4380T>A (p.Phe1460Leu) c.4011T>A (p.Phe1337Leu) n.4380T>A | |
| 13 | g.32338735T>C | CA483438286 | BRCA2 | c.4380T>C (p.Phe1460=) c.4011T>C (p.Phe1337=) n.4380T>C | |
| 13 | g.32338735T>G | CA387781050 | BRCA2 | c.4380T>G (p.Phe1460Leu) c.4011T>G (p.Phe1337Leu) n.4380T>G | |
| 13 | g.32338736T>A | CA387781051 | BRCA2 | c.4381T>A (p.Ser1461Thr) c.4012T>A (p.Ser1338Thr) n.4381T>A | dbSNP |
| 13 | g.32338736T>C | CA16613884 | BRCA2 | c.4381T>C (p.Ser1461Pro) c.4012T>C (p.Ser1338Pro) n.4381T>C | ClinVar dbSNP |
| 13 | g.32338736T>G | CA387781054 | BRCA2 | c.4381T>G (p.Ser1461Ala) c.4012T>G (p.Ser1338Ala) n.4381T>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338736T= | CA2082811218 | BRCA2 | c.4381T= (p.Ser1461=) c.4012T= (p.Ser1338=) n.4381T= | |
| 13 | g.32338737C>A | CA387781056 | BRCA2 | c.4382C>A (p.Ser1461Tyr) c.4013C>A (p.Ser1338Tyr) n.4382C>A | dbSNP |
| 13 | g.32338737C= | CA2082811246 | BRCA2 | c.4382C= (p.Ser1461=) c.4013C= (p.Ser1338=) n.4382C= | |
| 13 | g.32338737C>G | CA387781058 | BRCA2 | c.4382C>G (p.Ser1461Cys) c.4013C>G (p.Ser1338Cys) n.4382C>G | dbSNP |
| 13 | g.32338737C>T | CA387781059 | BRCA2 | c.4382C>T (p.Ser1461Phe) c.4013C>T (p.Ser1338Phe) n.4382C>T | ClinVar dbSNP |
| 13 | g.32338737_32338739delinsCCT | CA2082811244 | BRCA2 | c.4382_4384delinsCCT (p.Ser1461=) c.4013_4015delinsCCT (p.Ser1338=) n.4382_4384delinsCCT | |
| 13 | g.32338738C>A | CA483438287 | BRCA2 | c.4383C>A (p.Ser1461=) c.4014C>A (p.Ser1338=) n.4383C>A | ClinVar dbSNP |
| 13 | g.32338738C= | CA2082811254 | BRCA2 | c.4383C= (p.Ser1461=) c.4014C= (p.Ser1338=) n.4383C= | |
| 13 | g.32338738C>G | CA483438288 | BRCA2 | c.4383C>G (p.Ser1461=) c.4014C>G (p.Ser1338=) n.4383C>G | ClinVar dbSNP |
| 13 | g.32338738C>T | CA483438289 | BRCA2 | c.4383C>T (p.Ser1461=) c.4014C>T (p.Ser1338=) n.4383C>T | dbSNP |
| 13 | g.32338738_32338739del | CA10579614 | BRCA2 | c.4383_4384del (p.Leu1462LysfsTer3) c.4014_4015del (p.Leu1339LysfsTer3) n.4383_4384del | ClinVar dbSNP |
| 13 | g.32338739T>A | CA387781062 | BRCA2 | c.4384T>A (p.Leu1462Ile) c.4015T>A (p.Leu1339Ile) n.4384T>A | ClinVar dbSNP |
| 13 | g.32338739T>C | CA483438291 | BRCA2 | c.4384T>C (p.Leu1462=) c.4015T>C (p.Leu1339=) n.4384T>C | dbSNP |
| 13 | g.32338739T>G | CA387781064 | BRCA2 | c.4384T>G (p.Leu1462Val) c.4015T>G (p.Leu1339Val) n.4384T>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338739T= | CA2082811271 | BRCA2 | c.4384T= (p.Leu1462=) c.4015T= (p.Leu1339=) n.4384T= | |
| 13 | g.32338740dup | CA10589255 | BRCA2 | c.4385dup (p.Leu1462PhefsTer4) c.4016dup (p.Leu1339PhefsTer4) n.4385dup | ClinVar dbSNP |