SUSPENSION NOTICE:2024-08-07T19:00:00-0500 — 2024-09-25T08:00:00-0500
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.
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.32339243_32339296del | CA2697551768 | BRCA2 | c.4888_4941del (p.Ser1630_Thr1647del) c.4519_4572del (p.Ser1507_Thr1524del) n.4888_4941del | ClinVar |
| 13 | g.32339247_32339291delinsAAAGTATCTTTTTGAAAGTTAAAGTACATGAAAATGTAGAAAAAG | CA2082816821 | BRCA2 | c.4892_4936delinsAAAGTATCTTTTTGAAAGTTAAAGTACATGAAAATGTAGAAAAAG (p.Lys1631=) c.4523_4567delinsAAAGTATCTTTTTGAAAGTTAAAGTACATGAAAATGTAGAAAAAG (p.Lys1508=) n.4892_4936delinsAAAGTATCTTTTTGAAAGTTAAAGTACATGAAAATGTAGAAAAAG | |
| 13 | g.32339250_32339293del | CA913190948 | BRCA2 | c.4895_4938del (p.Ser1632AsnfsTer19) c.4526_4569del (p.Ser1509AsnfsTer19) n.4895_4938del | ClinVar dbSNP |
| 13 | g.32339273C>A | CA387783611 | BRCA2 | c.4918C>A (p.His1640Asn) c.4549C>A (p.His1517Asn) n.4918C>A | gnomAD v4 |
| 13 | g.32339273C= | CA2082817133 | BRCA2 | c.4918C= (p.His1640=) c.4549C= (p.His1517=) n.4918C= | |
| 13 | g.32339273C>G | CA387783612 | BRCA2 | c.4918C>G (p.His1640Asp) c.4549C>G (p.His1517Asp) n.4918C>G | |
| 13 | g.32339273C>T | CA6940826 | BRCA2 | c.4918C>T (p.His1640Tyr) c.4549C>T (p.His1517Tyr) n.4918C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32339273_32339276del | CA658761161 | BRCA2 | c.4918_4921del (p.His1640LysfsTer3) c.4549_4552del (p.His1517LysfsTer3) n.4918_4921del | |
| 13 | g.32339274A= | CA2082817147 | BRCA2 | c.4919A= (p.His1640=) c.4550A= (p.His1517=) n.4919A= | |
| 13 | g.32339274A>C | CA387783615 | BRCA2 | c.4919A>C (p.His1640Pro) c.4550A>C (p.His1517Pro) n.4919A>C | ClinVar dbSNP |
| 13 | g.32339274A>G | CA247508683 | BRCA2 | c.4919A>G (p.His1640Arg) c.4550A>G (p.His1517Arg) n.4919A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
| 13 | g.32339274A>T | CA387783617 | BRCA2 | c.4919A>T (p.His1640Leu) c.4550A>T (p.His1517Leu) n.4919A>T | dbSNP |
| 13 | g.32339275T>A | CA387783621 | BRCA2 | c.4920T>A (p.His1640Gln) c.4551T>A (p.His1517Gln) n.4920T>A | |
| 13 | g.32339275T>C | CA483438206 | BRCA2 | c.4920T>C (p.His1640=) c.4551T>C (p.His1517=) n.4920T>C | ClinVar dbSNP |
| 13 | g.32339275T>G | CA387783619 | BRCA2 | c.4920T>G (p.His1640Gln) c.4551T>G (p.His1517Gln) n.4920T>G | |
| 13 | g.32339275T= | CA2082817164 | BRCA2 | c.4920T= (p.His1640=) c.4551T= (p.His1517=) n.4920T= | |
| 13 | g.32339275_32339279delinsTGAAA | CA2082817158 | BRCA2 | c.4920_4924delinsTGAAA (p.His1640=) c.4551_4555delinsTGAAA (p.His1517=) n.4920_4924delinsTGAAA | |
| 13 | g.32339276G>A | CA387783623 | BRCA2 | c.4921G>A (p.Glu1641Lys) c.4552G>A (p.Glu1518Lys) n.4921G>A | |
| 13 | g.32339276G>C | CA387783624 | BRCA2 | c.4921G>C (p.Glu1641Gln) c.4552G>C (p.Glu1518Gln) n.4921G>C | dbSNP |
| 13 | g.32339276G= | CA2082817180 | BRCA2 | c.4921G= (p.Glu1641=) c.4552G= (p.Glu1518=) n.4921G= | |
| 13 | g.32339276G>T | CA387783625 | BRCA2 | c.4921G>T (p.Glu1641Ter) c.4552G>T (p.Glu1518Ter) n.4921G>T | ClinVar dbSNP |
| 13 | g.32339276_32339279del | CA021008 | BRCA2 | c.4921_4924del (p.Glu1641MetfsTer2) c.4552_4555del (p.Glu1518MetfsTer2) n.4921_4924del | ClinVar dbSNP |
| 13 | g.32339276_32339286delinsGAAAATGTAGA | CA2082817175 | BRCA2 | c.4921_4931delinsGAAAATGTAGA (p.Glu1641=) c.4552_4562delinsGAAAATGTAGA (p.Glu1518=) n.4921_4931delinsGAAAATGTAGA | |
| 13 | g.32339277A>C | CA387783628 | BRCA2 | c.4922A>C (p.Glu1641Ala) c.4553A>C (p.Glu1518Ala) n.4922A>C | |
| 13 | g.32339277A>G | CA387783630 | BRCA2 | c.4922A>G (p.Glu1641Gly) c.4553A>G (p.Glu1518Gly) n.4922A>G | ClinVar |
| 13 | g.32339277A>T | CA387783631 | BRCA2 | c.4922A>T (p.Glu1641Val) c.4553A>T (p.Glu1518Val) n.4922A>T | dbSNP |
| 13 | g.32339281_32339290del | CA021017 | BRCA2 | c.4926_4935del (p.Asn1642LysfsTer25) c.4557_4566del (p.Asn1519LysfsTer25) n.4926_4935del | ClinVar dbSNP |
| 13 | g.32339278A= | CA2082817193 | BRCA2 | c.4923A= (p.Glu1641=) c.4554A= (p.Glu1518=) n.4923A= | |
| 13 | g.32339278A>C | CA387783633 | BRCA2 | c.4923A>C (p.Glu1641Asp) c.4554A>C (p.Glu1518Asp) n.4923A>C | ClinVar dbSNP |
| 13 | g.32339278A>G | CA483438214 | BRCA2 | c.4923A>G (p.Glu1641=) c.4554A>G (p.Glu1518=) n.4923A>G | gnomAD v4 |
| 13 | g.32339278A>T | CA387783635 | BRCA2 | c.4923A>T (p.Glu1641Asp) c.4554A>T (p.Glu1518Asp) n.4923A>T | dbSNP |
| 13 | g.32339279A>C | CA387783636 | BRCA2 | c.4924A>C (p.Asn1642His) c.4555A>C (p.Asn1519His) n.4924A>C | dbSNP |
| 13 | g.32339279A>G | CA387783638 | BRCA2 | c.4924A>G (p.Asn1642Asp) c.4555A>G (p.Asn1519Asp) n.4924A>G | |
| 13 | g.32339279A>T | CA387783639 | BRCA2 | c.4924A>T (p.Asn1642Tyr) c.4555A>T (p.Asn1519Tyr) n.4924A>T | dbSNP |
| 13 | g.32339280A= | CA2082817201 | BRCA2 | c.4925A= (p.Asn1642=) c.4556A= (p.Asn1519=) n.4925A= | |
| 13 | g.32339280A>C | CA021014 | BRCA2 | c.4925A>C (p.Asn1642Thr) c.4556A>C (p.Asn1519Thr) n.4925A>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32339280A>G | CA387783641 | BRCA2 | c.4925A>G (p.Asn1642Ser) c.4556A>G (p.Asn1519Ser) n.4925A>G | gnomAD v4 |
| 13 | g.32339280A>T | CA387783640 | BRCA2 | c.4925A>T (p.Asn1642Ile) c.4556A>T (p.Asn1519Ile) n.4925A>T | dbSNP |
| 13 | g.32339280_32339282delinsATG | CA2082817206 | BRCA2 | c.4925_4927delinsATG (p.Asn1642=) c.4556_4558delinsATG (p.Asn1519=) n.4925_4927delinsATG | |
| 13 | g.32339281T>A | CA387783643 | BRCA2 | c.4926T>A (p.Asn1642Lys) c.4557T>A (p.Asn1519Lys) n.4926T>A | |
| 13 | g.32339281T>C | CA16606684 | BRCA2 | c.4926T>C (p.Asn1642=) c.4557T>C (p.Asn1519=) n.4926T>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32339281T>G | CA387783644 | BRCA2 | c.4926T>G (p.Asn1642Lys) c.4557T>G (p.Asn1519Lys) n.4926T>G | |
| 13 | g.32339281T= | CA2082817217 | BRCA2 | c.4926T= (p.Asn1642=) c.4557T= (p.Asn1519=) n.4926T= | |
| 13 | g.32339282_32339283del | CA916080552 | BRCA2 | c.4927_4928del (p.Val1643ArgfsTer22) c.4558_4559del (p.Val1520ArgfsTer22) n.4927_4928del | ClinVar dbSNP |
| 13 | g.32339282del | CA2695217884 | BRCA2 | c.4927del (p.Val1643Ter) c.4558del (p.Val1520Ter) n.4927del | |
| 13 | g.32339282G>A | CA10584447 | BRCA2 | c.4927G>A (p.Val1643Ile) c.4558G>A (p.Val1520Ile) n.4927G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32339282G>C | CA387783647 | BRCA2 | c.4927G>C (p.Val1643Leu) c.4558G>C (p.Val1520Leu) n.4927G>C | dbSNP |
| 13 | g.32339282G= | CA2082817224 | BRCA2 | c.4927G= (p.Val1643=) c.4558G= (p.Val1520=) n.4927G= | |
| 13 | g.32339282G>T | CA387783649 | BRCA2 | c.4927G>T (p.Val1643Leu) c.4558G>T (p.Val1520Leu) n.4927G>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32339283T>A | CA387783650 | BRCA2 | c.4928T>A (p.Val1643Glu) c.4559T>A (p.Val1520Glu) n.4928T>A | ClinVar |
| 13 | g.32339283T>C | CA021023 | BRCA2 | c.4928T>C (p.Val1643Ala) c.4559T>C (p.Val1520Ala) n.4928T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32339283T>G | CA387783652 | BRCA2 | c.4928T>G (p.Val1643Gly) c.4559T>G (p.Val1520Gly) n.4928T>G | |
| 13 | g.32339283T= | CA2082817244 | BRCA2 | c.4928T= (p.Val1643=) c.4559T= (p.Val1520=) n.4928T= | |
| 13 | g.32339283_32339288del | CA2573149298 | BRCA2 | c.4928_4933del (p.Val1643_Lys1645delinsGlu) c.4559_4564del (p.Val1520_Lys1522delinsGlu) n.4928_4933del | dbSNP |
| 13 | g.32339283_32339291delinsTAGAAAAAG | CA2082817240 | BRCA2 | c.4928_4936delinsTAGAAAAAG (p.Val1643=) c.4559_4567delinsTAGAAAAAG (p.Val1520=) n.4928_4936delinsTAGAAAAAG | |
| 13 | g.32339284A= | CA2082817259 | BRCA2 | c.4929A= (p.Val1643=) c.4560A= (p.Val1520=) n.4929A= | |
| 13 | g.32339284A>C | CA483438232 | BRCA2 | c.4929A>C (p.Val1643=) c.4560A>C (p.Val1520=) n.4929A>C | |
| 13 | g.32339284A>G | CA10579638 | BRCA2 | c.4929A>G (p.Val1643=) c.4560A>G (p.Val1520=) n.4929A>G | ClinVar dbSNP |
| 13 | g.32339284A>T | CA483438233 | BRCA2 | c.4929A>T (p.Val1643=) c.4560A>T (p.Val1520=) n.4929A>T | dbSNP |
| 13 | g.32339285_32339292del | CA10589277 | BRCA2 | c.4930_4937del (p.Glu1644AsnfsTer19) c.4561_4568del (p.Glu1521AsnfsTer19) n.4930_4937del | ClinVar dbSNP |
| 13 | g.32339285G>A | CA387783660 | BRCA2 | c.4930G>A (p.Glu1644Lys) c.4561G>A (p.Glu1521Lys) n.4930G>A | dbSNP |
| 13 | g.32339285G>C | CA387783657 | BRCA2 | c.4930G>C (p.Glu1644Gln) c.4561G>C (p.Glu1521Gln) n.4930G>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32339285G= | CA2082817284 | BRCA2 | c.4930G= (p.Glu1644=) c.4561G= (p.Glu1521=) n.4930G= | |
| 13 | g.32339285G>T | CA387783659 | BRCA2 | c.4930G>T (p.Glu1644Ter) c.4561G>T (p.Glu1521Ter) n.4930G>T | dbSNP |
| 13 | g.32339285_32339288delinsGAAA | CA2082817265 | BRCA2 | c.4930_4933delinsGAAA (p.Glu1644=) c.4561_4564delinsGAAA (p.Glu1521=) n.4930_4933delinsGAAA | |
| 13 | g.32339286A>C | CA387783663 | BRCA2 | c.4931A>C (p.Glu1644Ala) c.4562A>C (p.Glu1521Ala) n.4931A>C | gnomAD v4 |
| 13 | g.32339286A>G | CA387783664 | BRCA2 | c.4931A>G (p.Glu1644Gly) c.4562A>G (p.Glu1521Gly) n.4931A>G | ClinVar |
| 13 | g.32339286A>T | CA387783666 | BRCA2 | c.4931A>T (p.Glu1644Val) c.4562A>T (p.Glu1521Val) n.4931A>T | dbSNP |
| 13 | g.32339290del | CA021030 | BRCA2 | c.4935del (p.Glu1646LysfsTer24) c.4566del (p.Glu1523LysfsTer24) n.4935del | ClinVar dbSNP |
| 13 | g.32339288_32339290del | CA6940827 | BRCA2 | c.4933_4935del (p.Lys1645del) c.4564_4566del (p.Lys1522del) n.4933_4935del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32339287A>C | CA387783673 | BRCA2 | c.4932A>C (p.Glu1644Asp) c.4563A>C (p.Glu1521Asp) n.4932A>C | dbSNP |
| 13 | g.32339287A>G | CA483438239 | BRCA2 | c.4932A>G (p.Glu1644=) c.4563A>G (p.Glu1521=) n.4932A>G | |
| 13 | g.32339287A>T | CA387783671 | BRCA2 | c.4932A>T (p.Glu1644Asp) c.4563A>T (p.Glu1521Asp) n.4932A>T | dbSNP |
| 13 | g.32339287_32339291delinsAAAAG | CA2082817301 | BRCA2 | c.4932_4936delinsAAAAG (p.Glu1644=) c.4563_4567delinsAAAAG (p.Glu1521=) n.4932_4936delinsAAAAG | |
| 13 | g.32339288A= | CA2082817313 | BRCA2 | c.4933A= (p.Lys1645=) c.4564A= (p.Lys1522=) n.4933A= | |
| 13 | g.32339288A>C | CA387783677 | BRCA2 | c.4933A>C (p.Lys1645Gln) c.4564A>C (p.Lys1522Gln) n.4933A>C | |
| 13 | g.32339288A>G | CA387783675 | BRCA2 | c.4933A>G (p.Lys1645Glu) c.4564A>G (p.Lys1522Glu) n.4933A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32339288A>T | CA021026 | BRCA2 | c.4933A>T (p.Lys1645Ter) c.4564A>T (p.Lys1522Ter) n.4933A>T | ClinVar dbSNP |
| 13 | g.32339288_32339291delinsAAAG | CA2082817308 | BRCA2 | c.4933_4936delinsAAAG (p.Lys1645=) c.4564_4567delinsAAAG (p.Lys1522=) n.4933_4936delinsAAAG | |
| 13 | g.32339291_32339294del | CA021036 | BRCA2 | c.4936_4939del (p.Glu1646GlnfsTer23) c.4567_4570del (p.Glu1523GlnfsTer23) n.4936_4939del | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339289A= | CA2082817334 | BRCA2 | c.4934A= (p.Lys1645=) c.4565A= (p.Lys1522=) n.4934A= | |
| 13 | g.32339289A>C | CA387783680 | BRCA2 | c.4934A>C (p.Lys1645Thr) c.4565A>C (p.Lys1522Thr) n.4934A>C | dbSNP |
| 13 | g.32339289A>G | CA387783683 | BRCA2 | c.4934A>G (p.Lys1645Arg) c.4565A>G (p.Lys1522Arg) n.4934A>G | |
| 13 | g.32339289A>T | CA387783684 | BRCA2 | c.4934A>T (p.Lys1645Ile) c.4565A>T (p.Lys1522Ile) n.4934A>T | dbSNP |
| 13 | g.32339289_32339291delinsAAG | CA2082817332 | BRCA2 | c.4934_4936delinsAAG (p.Lys1645=) c.4565_4567delinsAAG (p.Lys1522=) n.4934_4936delinsAAG | |
| 13 | g.32339291_32339293del | CA6940828 | BRCA2 | c.4936_4938del (p.Glu1646del) c.4567_4569del (p.Glu1523del) n.4936_4938del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32339290A>C | CA387783687 | BRCA2 | c.4935A>C (p.Lys1645Asn) c.4566A>C (p.Lys1522Asn) n.4935A>C | dbSNP |
| 13 | g.32339290A>G | CA483438251 | BRCA2 | c.4935A>G (p.Lys1645=) c.4566A>G (p.Lys1522=) n.4935A>G | ClinVar dbSNP |
| 13 | g.32339290A>T | CA387783689 | BRCA2 | c.4935A>T (p.Lys1645Asn) c.4566A>T (p.Lys1522Asn) n.4935A>T | dbSNP |
| 13 | g.32339290_32339291delinsT | CA915948476 | BRCA2 | c.4935_4936delinsT (p.Lys1645AsnfsTer25) c.4566_4567delinsT (p.Lys1522AsnfsTer25) n.4935_4936delinsT | ClinVar dbSNP |
| 13 | g.32339290_32339291delinsAG | CA2082817349 | BRCA2 | c.4935_4936delinsAG (p.Lys1645=) c.4566_4567delinsAG (p.Lys1522=) n.4935_4936delinsAG | |
| 13 | g.32339291_32339292del | CA021033 | BRCA2 | c.4936_4937del (p.Glu1646AsnfsTer19) c.4567_4568del (p.Glu1523AsnfsTer19) n.4936_4937del | ClinVar dbSNP |
| 13 | g.32339291del | CA6940829 | BRCA2 | c.4936del (p.Glu1646LysfsTer24) c.4567del (p.Glu1523LysfsTer24) n.4936del | ClinVar dbSNP ExAC gnomAD v2 |
| 13 | g.32339291G>A | CA387783691 | BRCA2 | c.4936G>A (p.Glu1646Lys) c.4567G>A (p.Glu1523Lys) n.4936G>A | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32339291G>C | CA387783693 | BRCA2 | c.4936G>C (p.Glu1646Gln) c.4567G>C (p.Glu1523Gln) n.4936G>C | ClinVar dbSNP COSMIC COSMIC |
| 13 | g.32339291G= | CA2082817361 | BRCA2 | c.4936G= (p.Glu1646=) c.4567G= (p.Glu1523=) n.4936G= | |
| 13 | g.32339291G>T | CA10586529 | BRCA2 | c.4936G>T (p.Glu1646Ter) c.4567G>T (p.Glu1523Ter) n.4936G>T | ClinVar dbSNP |
| 13 | g.32339292A= | CA2082817373 | BRCA2 | c.4937A= (p.Glu1646=) c.4568A= (p.Glu1523=) n.4937A= | |
| 13 | g.32339292A>C | CA6940830 | BRCA2 | c.4937A>C (p.Glu1646Ala) c.4568A>C (p.Glu1523Ala) n.4937A>C | dbSNP ExAC gnomAD v2 |
| 13 | g.32339292A>G | CA387783696 | BRCA2 | c.4937A>G (p.Glu1646Gly) c.4568A>G (p.Glu1523Gly) n.4937A>G | ClinVar dbSNP |
| 13 | g.32339292A>T | CA387783698 | BRCA2 | c.4937A>T (p.Glu1646Val) c.4568A>T (p.Glu1523Val) n.4937A>T | |
| 13 | g.32339294dup | CA10589278 | BRCA2 | c.4939dup (p.Thr1647AsnfsTer19) c.4570dup (p.Thr1524AsnfsTer19) n.4939dup | ClinVar dbSNP |
| 13 | g.32339295_32339301del | CA2580087319 | BRCA2 | c.4940_4946del (p.Thr1647LysfsTer21) c.4571_4577del (p.Thr1524LysfsTer21) n.4940_4946del | ClinVar |
| 13 | g.32339293A= | CA2082817385 | BRCA2 | c.4938A= (p.Glu1646=) c.4569A= (p.Glu1523=) n.4938A= | |
| 13 | g.32339293A>C | CA387783699 | BRCA2 | c.4938A>C (p.Glu1646Asp) c.4569A>C (p.Glu1523Asp) n.4938A>C | dbSNP |
| 13 | g.32339293A>G | CA349941 | BRCA2 | c.4938A>G (p.Glu1646=) c.4569A>G (p.Glu1523=) n.4938A>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32339293A>T | CA387783703 | BRCA2 | c.4938A>T (p.Glu1646Asp) c.4569A>T (p.Glu1523Asp) n.4938A>T | dbSNP |
| 13 | g.32339293_32339295delinsAAC | CA2082817380 | BRCA2 | c.4938_4940delinsAAC (p.Glu1646=) c.4569_4571delinsAAC (p.Glu1523=) n.4938_4940delinsAAC | |
| 13 | g.32339294A= | CA2082817400 | BRCA2 | c.4939A= (p.Thr1647=) c.4570A= (p.Thr1524=) n.4939A= | |
| 13 | g.32339294A>C | CA387783704 | BRCA2 | c.4939A>C (p.Thr1647Pro) c.4570A>C (p.Thr1524Pro) n.4939A>C | dbSNP |
| 13 | g.32339294A>G | CA387783705 | BRCA2 | c.4939A>G (p.Thr1647Ala) c.4570A>G (p.Thr1524Ala) n.4939A>G | ClinVar dbSNP |
| 13 | g.32339294A>T | CA387783706 | BRCA2 | c.4939A>T (p.Thr1647Ser) c.4570A>T (p.Thr1524Ser) n.4939A>T | dbSNP |
| 13 | g.32339294_32339295delinsAC | CA2082817403 | BRCA2 | c.4939_4940delinsAC (p.Thr1647=) c.4570_4571delinsAC (p.Thr1524=) n.4939_4940delinsAC | |
| 13 | g.32339295_32339296del | CA021044 | BRCA2 | c.4940_4941del (p.Thr1647SerfsTer18) c.4571_4572del (p.Thr1524SerfsTer18) n.4940_4941del | ClinVar dbSNP |
| 13 | g.32339295del | CA10586530 | BRCA2 | c.4940del (p.Thr1647LysfsTer23) c.4571del (p.Thr1524LysfsTer23) n.4940del | ClinVar dbSNP |
| 13 | g.32339295C>A | CA387783713 | BRCA2 | c.4940C>A (p.Thr1647Lys) c.4571C>A (p.Thr1524Lys) n.4940C>A | ClinVar dbSNP |
| 13 | g.32339295C= | CA2082817416 | BRCA2 | c.4940C= (p.Thr1647=) c.4571C= (p.Thr1524=) n.4940C= | |
| 13 | g.32339295C>G | CA387783709 | BRCA2 | c.4940C>G (p.Thr1647Arg) c.4571C>G (p.Thr1524Arg) n.4940C>G | ClinVar dbSNP |
| 13 | g.32339295C>T | CA387783711 | BRCA2 | c.4940C>T (p.Thr1647Ile) c.4571C>T (p.Thr1524Ile) n.4940C>T | ClinVar dbSNP |
| 13 | g.32339296A= | CA2082817428 | BRCA2 | c.4941A= (p.Thr1647=) c.4572A= (p.Thr1524=) n.4941A= | |
| 13 | g.32339296A>C | CA483438262 | BRCA2 | c.4941A>C (p.Thr1647=) c.4572A>C (p.Thr1524=) n.4941A>C | ClinVar |
| 13 | g.32339296A>G | CA10579639 | BRCA2 | c.4941A>G (p.Thr1647=) c.4572A>G (p.Thr1524=) n.4941A>G | ClinVar dbSNP |
| 13 | g.32339296A>T | CA483438263 | BRCA2 | c.4941A>T (p.Thr1647=) c.4572A>T (p.Thr1524=) n.4941A>T | dbSNP |
| 13 | g.32339297G>A | CA021048 | BRCA2 | c.4942G>A (p.Ala1648Thr) c.4573G>A (p.Ala1525Thr) n.4942G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339297G>C | CA387783715 | BRCA2 | c.4942G>C (p.Ala1648Pro) c.4573G>C (p.Ala1525Pro) n.4942G>C | dbSNP |
| 13 | g.32339297G= | CA2082817440 | BRCA2 | c.4942G= (p.Ala1648=) c.4573G= (p.Ala1525=) n.4942G= | |
| 13 | g.32339297G>T | CA387783717 | BRCA2 | c.4942G>T (p.Ala1648Ser) c.4573G>T (p.Ala1525Ser) n.4942G>T | |
| 13 | g.32339298del | CA2499222182 | BRCA2 | c.4943del (p.Ala1648GlufsTer22) c.4574del (p.Ala1525GlufsTer22) n.4943del | ClinVar dbSNP |
| 13 | g.32339298C>A | CA387783719 | BRCA2 | c.4943C>A (p.Ala1648Glu) c.4574C>A (p.Ala1525Glu) n.4943C>A | ClinVar dbSNP gnomAD v2 |
| 13 | g.32339298C= | CA2082817456 | BRCA2 | c.4943C= (p.Ala1648=) c.4574C= (p.Ala1525=) n.4943C= | |
| 13 | g.32339298C>G | CA387783720 | BRCA2 | c.4943C>G (p.Ala1648Gly) c.4574C>G (p.Ala1525Gly) n.4943C>G | gnomAD v4 |
| 13 | g.32339298C>T | CA387783721 | BRCA2 | c.4943C>T (p.Ala1648Val) c.4574C>T (p.Ala1525Val) n.4943C>T | ClinVar dbSNP |
| 13 | g.32339298_32339300delinsCAA | CA2082817460 | BRCA2 | c.4943_4945delinsCAA (p.Ala1648=) c.4574_4576delinsCAA (p.Ala1525=) n.4943_4945delinsCAA | |
| 13 | g.32339299A>C | CA483438265 | BRCA2 | c.4944A>C (p.Ala1648=) c.4575A>C (p.Ala1525=) n.4944A>C | |
| 13 | g.32339299A>G | CA483438267 | BRCA2 | c.4944A>G (p.Ala1648=) c.4575A>G (p.Ala1525=) n.4944A>G | |
| 13 | g.32339299A>T | CA483438268 | BRCA2 | c.4944A>T (p.Ala1648=) c.4575A>T (p.Ala1525=) n.4944A>T | |
| 13 | g.32339303del | CA483438266 | BRCA2 | c.4948del (p.Ser1650ValfsTer20) c.4579del (p.Ser1527ValfsTer20) n.4948del | ClinVar dbSNP COSMIC COSMIC |
| 13 | g.32339302_32339303del | CA021051 | BRCA2 | c.4947_4948del (p.Pro1651CysfsTer14) c.4578_4579del (p.Pro1528CysfsTer14) n.4947_4948del | ClinVar dbSNP |
| 13 | g.32339300A= | CA2082817474 | BRCA2 | c.4945A= (p.Lys1649=) c.4576A= (p.Lys1526=) n.4945A= | |
| 13 | g.32339300A>C | CA387783726 | BRCA2 | c.4945A>C (p.Lys1649Gln) c.4576A>C (p.Lys1526Gln) n.4945A>C | dbSNP |
| 13 | g.32339300A>G | CA6940831 | BRCA2 | c.4945A>G (p.Lys1649Glu) c.4576A>G (p.Lys1526Glu) n.4945A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32339300A>T | CA387783725 | BRCA2 | c.4945A>T (p.Lys1649Ter) c.4576A>T (p.Lys1526Ter) n.4945A>T | dbSNP COSMIC |
| 13 | g.32339301A>C | CA387783733 | BRCA2 | c.4946A>C (p.Lys1649Thr) c.4577A>C (p.Lys1526Thr) n.4946A>C | |
| 13 | g.32339301A>G | CA387783734 | BRCA2 | c.4946A>G (p.Lys1649Arg) c.4577A>G (p.Lys1526Arg) n.4946A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339301A>T | CA387783736 | BRCA2 | c.4946A>T (p.Lys1649Ile) c.4577A>T (p.Lys1526Ile) n.4946A>T | dbSNP |
| 13 | g.32339302A>C | CA387783737 | BRCA2 | c.4947A>C (p.Lys1649Asn) c.4578A>C (p.Lys1526Asn) n.4947A>C | ClinVar dbSNP |
| 13 | g.32339302A>G | CA483438272 | BRCA2 | c.4947A>G (p.Lys1649=) c.4578A>G (p.Lys1526=) n.4947A>G | dbSNP |
| 13 | g.32339302A>T | CA387783738 | BRCA2 | c.4947A>T (p.Lys1649Asn) c.4578A>T (p.Lys1526Asn) n.4947A>T | dbSNP |
| 13 | g.32339303A>C | CA387783746 | BRCA2 | c.4948A>C (p.Ser1650Arg) c.4579A>C (p.Ser1527Arg) n.4948A>C | |
| 13 | g.32339303A>G | CA387783740 | BRCA2 | c.4948A>G (p.Ser1650Gly) c.4579A>G (p.Ser1527Gly) n.4948A>G | |
| 13 | g.32339303A>T | CA387783742 | BRCA2 | c.4948A>T (p.Ser1650Cys) c.4579A>T (p.Ser1527Cys) n.4948A>T | ClinVar dbSNP |
| 13 | g.32339303_32339304delinsAG | CA2082817486 | BRCA2 | c.4948_4949delinsAG (p.Ser1650=) c.4579_4580delinsAG (p.Ser1527=) n.4948_4949delinsAG | |
| 13 | g.32339304del | CA915948477 | BRCA2 | c.4949del (p.Ser1650IlefsTer20) c.4580del (p.Ser1527IlefsTer20) n.4949del | ClinVar dbSNP |
| 13 | g.32339304G>A | CA387783748 | BRCA2 | c.4949G>A (p.Ser1650Asn) c.4580G>A (p.Ser1527Asn) n.4949G>A | dbSNP gnomAD v4 |
| 13 | g.32339304G>C | CA387783750 | BRCA2 | c.4949G>C (p.Ser1650Thr) c.4580G>C (p.Ser1527Thr) n.4949G>C | dbSNP |
| 13 | g.32339304G>T | CA387783751 | BRCA2 | c.4949G>T (p.Ser1650Ile) c.4580G>T (p.Ser1527Ile) n.4949G>T | |
| 13 | g.32339305T>A | CA387783753 | BRCA2 | c.4950T>A (p.Ser1650Arg) c.4581T>A (p.Ser1527Arg) n.4950T>A | dbSNP |
| 13 | g.32339305T>C | CA483438274 | BRCA2 | c.4950T>C (p.Ser1650=) c.4581T>C (p.Ser1527=) n.4950T>C | |
| 13 | g.32339305T>G | CA387783754 | BRCA2 | c.4950T>G (p.Ser1650Arg) c.4581T>G (p.Ser1527Arg) n.4950T>G | dbSNP |
| 13 | g.32339305_32339306delinsTC | CA2082817495 | BRCA2 | c.4950_4951delinsTC (p.Ser1650=) c.4581_4582delinsTC (p.Ser1527=) n.4950_4951delinsTC | |
| 13 | g.32339306C>A | CA387783759 | BRCA2 | c.4951C>A (p.Pro1651Thr) c.4582C>A (p.Pro1528Thr) n.4951C>A | dbSNP |
| 13 | g.32339306C= | CA2082817501 | BRCA2 | c.4951C= (p.Pro1651=) c.4582C= (p.Pro1528=) n.4951C= | |
| 13 | g.32339306C>G | CA387783757 | BRCA2 | c.4951C>G (p.Pro1651Ala) c.4582C>G (p.Pro1528Ala) n.4951C>G | |
| 13 | g.32339306C>T | CA6940832 | BRCA2 | c.4951C>T (p.Pro1651Ser) c.4582C>T (p.Pro1528Ser) n.4951C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32339307del | CA021054 | BRCA2 | c.4952del (p.Pro1651LeufsTer19) c.4583del (p.Pro1528LeufsTer19) n.4952del | ClinVar dbSNP |
| 13 | g.32339307C>A | CA387783760 | BRCA2 | c.4952C>A (p.Pro1651His) c.4583C>A (p.Pro1528His) n.4952C>A | ClinVar dbSNP |
| 13 | g.32339307C= | CA2082817516 | BRCA2 | c.4952C= (p.Pro1651=) c.4583C= (p.Pro1528=) n.4952C= | |
| 13 | g.32339307C>G | CA387783762 | BRCA2 | c.4952C>G (p.Pro1651Arg) c.4583C>G (p.Pro1528Arg) n.4952C>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32339307C>T | CA6940833 | BRCA2 | c.4952C>T (p.Pro1651Leu) c.4583C>T (p.Pro1528Leu) n.4952C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32339308T>A | CA483438276 | BRCA2 | c.4953T>A (p.Pro1651=) c.4584T>A (p.Pro1528=) n.4953T>A | dbSNP |
| 13 | g.32339308T>C | CA6940834 | BRCA2 | c.4953T>C (p.Pro1651=) c.4584T>C (p.Pro1528=) n.4953T>C | ClinVar dbSNP ExAC gnomAD v2 |
| 13 | g.32339308T>G | CA483438277 | BRCA2 | c.4953T>G (p.Pro1651=) c.4584T>G (p.Pro1528=) n.4953T>G | |
| 13 | g.32339308T= | CA2082817528 | BRCA2 | c.4953T= (p.Pro1651=) c.4584T= (p.Pro1528=) n.4953T= | |
| 13 | g.32339309G>A | CA387783769 | BRCA2 | c.4954G>A (p.Ala1652Thr) c.4585G>A (p.Ala1529Thr) n.4954G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339309G>C | CA021057 | BRCA2 | c.4954G>C (p.Ala1652Pro) c.4585G>C (p.Ala1529Pro) n.4954G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32339309G= | CA2082817533 | BRCA2 | c.4954G= (p.Ala1652=) c.4585G= (p.Ala1529=) n.4954G= | |
| 13 | g.32339309G>T | CA387783766 | BRCA2 | c.4954G>T (p.Ala1652Ser) c.4585G>T (p.Ala1529Ser) n.4954G>T | dbSNP |
| 13 | g.32339310C>A | CA387783771 | BRCA2 | c.4955C>A (p.Ala1652Glu) c.4586C>A (p.Ala1529Glu) n.4955C>A | dbSNP |
| 13 | g.32339310C>G | CA387783772 | BRCA2 | c.4955C>G (p.Ala1652Gly) c.4586C>G (p.Ala1529Gly) n.4955C>G | dbSNP |
| 13 | g.32339310C>T | CA387783773 | BRCA2 | c.4955C>T (p.Ala1652Val) c.4586C>T (p.Ala1529Val) n.4955C>T | gnomAD v4 |
| 13 | g.32339311A>C | CA483438278 | BRCA2 | c.4956A>C (p.Ala1652=) c.4587A>C (p.Ala1529=) n.4956A>C | dbSNP |
| 13 | g.32339311A>G | CA483438279 | BRCA2 | c.4956A>G (p.Ala1652=) c.4587A>G (p.Ala1529=) n.4956A>G | dbSNP gnomAD v4 |
| 13 | g.32339311A>T | CA483438280 | BRCA2 | c.4956A>T (p.Ala1652=) c.4587A>T (p.Ala1529=) n.4956A>T | dbSNP |
| 13 | g.32339312A= | CA2082817543 | BRCA2 | c.4957A= (p.Thr1653=) c.4588A= (p.Thr1530=) n.4957A= | |
| 13 | g.32339312A>C | CA387783775 | BRCA2 | c.4957A>C (p.Thr1653Pro) c.4588A>C (p.Thr1530Pro) n.4957A>C | dbSNP |
| 13 | g.32339312A>G | CA021061 | BRCA2 | c.4957A>G (p.Thr1653Ala) c.4588A>G (p.Thr1530Ala) n.4957A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339312A>T | CA387783777 | BRCA2 | c.4957A>T (p.Thr1653Ser) c.4588A>T (p.Thr1530Ser) n.4957A>T | dbSNP |
| 13 | g.32339313C>A | CA387783779 | BRCA2 | c.4958C>A (p.Thr1653Asn) c.4589C>A (p.Thr1530Asn) n.4958C>A | |
| 13 | g.32339313C= | CA2082817553 | BRCA2 | c.4958C= (p.Thr1653=) c.4589C= (p.Thr1530=) n.4958C= | |
| 13 | g.32339313C>G | CA387783782 | BRCA2 | c.4958C>G (p.Thr1653Ser) c.4589C>G (p.Thr1530Ser) n.4958C>G | dbSNP |
| 13 | g.32339313C>T | CA387783780 | BRCA2 | c.4958C>T (p.Thr1653Ile) c.4589C>T (p.Thr1530Ile) n.4958C>T | ClinVar dbSNP |
| 13 | g.32339314T>A | CA483438281 | BRCA2 | c.4959T>A (p.Thr1653=) c.4590T>A (p.Thr1530=) n.4959T>A | dbSNP |
| 13 | g.32339314T>C | CA483438282 | BRCA2 | c.4959T>C (p.Thr1653=) c.4590T>C (p.Thr1530=) n.4959T>C | dbSNP |
| 13 | g.32339314T>G | CA483438283 | BRCA2 | c.4959T>G (p.Thr1653=) c.4590T>G (p.Thr1530=) n.4959T>G | |
| 13 | g.32339315dup | CA10589279 | BRCA2 | c.4960dup (p.Cys1654LeufsTer12) c.4591dup (p.Cys1531LeufsTer12) n.4960dup | ClinVar dbSNP |
| 13 | g.32339314_32339318delinsG | CA2825002151 | BRCA2 | c.4959_4963delinsG (p.Cys1654ThrfsTer15) c.4590_4594delinsG (p.Cys1531ThrfsTer15) n.4959_4963delinsG | ClinVar |
| 13 | g.32339315T>A | CA387783785 | BRCA2 | c.4960T>A (p.Cys1654Ser) c.4591T>A (p.Cys1531Ser) n.4960T>A | |
| 13 | g.32339315T>C | CA387783786 | BRCA2 | c.4960T>C (p.Cys1654Arg) c.4591T>C (p.Cys1531Arg) n.4960T>C | ClinVar |
| 13 | g.32339315T>G | CA10579640 | BRCA2 | c.4960T>G (p.Cys1654Gly) c.4591T>G (p.Cys1531Gly) n.4960T>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339315T= | CA2082817565 | BRCA2 | c.4960T= (p.Cys1654=) c.4591T= (p.Cys1531=) n.4960T= | |
| 13 | g.32339316_32339326del | CA2573149304 | BRCA2 | c.4961_4971del (p.Cys1654SerfsTer8) c.4592_4602del (p.Cys1531SerfsTer8) n.4961_4971del | ClinVar dbSNP |
| 13 | g.32339316G>A | CA387783787 | BRCA2 | c.4961G>A (p.Cys1654Tyr) c.4592G>A (p.Cys1531Tyr) n.4961G>A | |
| 13 | g.32339316G>C | CA387783788 | BRCA2 | c.4961G>C (p.Cys1654Ser) c.4592G>C (p.Cys1531Ser) n.4961G>C | |
| 13 | g.32339316G>T | CA387783789 | BRCA2 | c.4961G>T (p.Cys1654Phe) c.4592G>T (p.Cys1531Phe) n.4961G>T | |
| 13 | g.32339316_32339317delinsGT | CA2082817572 | BRCA2 | c.4961_4962delinsGT (p.Cys1654=) c.4592_4593delinsGT (p.Cys1531=) n.4961_4962delinsGT | |
| 13 | g.32339317T>A | CA16043338 | BRCA2 | c.4962T>A (p.Cys1654Ter) c.4593T>A (p.Cys1531Ter) n.4962T>A | ClinVar dbSNP |
| 13 | g.32339317T>C | CA483438285 | BRCA2 | c.4962T>C (p.Cys1654=) c.4593T>C (p.Cys1531=) n.4962T>C | |
| 13 | g.32339317T>G | CA387783791 | BRCA2 | c.4962T>G (p.Cys1654Trp) c.4593T>G (p.Cys1531Trp) n.4962T>G | dbSNP |
| 13 | g.32339317T= | CA2082817580 | BRCA2 | c.4962T= (p.Cys1654=) c.4593T= (p.Cys1531=) n.4962T= | |
| 13 | g.32339318dup | CA2695217885 | BRCA2 | c.4963dup (p.Tyr1655LeufsTer11) c.4594dup (p.Tyr1532LeufsTer11) n.4963dup | |
| 13 | g.32339318del | CA10575849 | BRCA2 | c.4963del (p.Tyr1655ThrfsTer15) c.4594del (p.Tyr1532ThrfsTer15) n.4963del | ClinVar dbSNP |
| 13 | g.32339318T>A | CA387783794 | BRCA2 | c.4963T>A (p.Tyr1655Asn) c.4594T>A (p.Tyr1532Asn) n.4963T>A | ClinVar dbSNP |
| 13 | g.32339318T>C | CA387783795 | BRCA2 | c.4963T>C (p.Tyr1655His) c.4594T>C (p.Tyr1532His) n.4963T>C | ClinVar dbSNP |
| 13 | g.32339318T>G | CA387783796 | BRCA2 | c.4963T>G (p.Tyr1655Asp) c.4594T>G (p.Tyr1532Asp) n.4963T>G | |
| 13 | g.32339318T= | CA2082817593 | BRCA2 | c.4963T= (p.Tyr1655=) c.4594T= (p.Tyr1532=) n.4963T= | |
| 13 | g.32339319A>C | CA387783802 | BRCA2 | c.4964A>C (p.Tyr1655Ser) c.4595A>C (p.Tyr1532Ser) n.4964A>C | dbSNP |
| 13 | g.32339319A>G | CA387783801 | BRCA2 | c.4964A>G (p.Tyr1655Cys) c.4595A>G (p.Tyr1532Cys) n.4964A>G | dbSNP |
| 13 | g.32339319A>T | CA387783799 | BRCA2 | c.4964A>T (p.Tyr1655Phe) c.4595A>T (p.Tyr1532Phe) n.4964A>T | dbSNP |
| 13 | g.32339319dup | CA021064 | BRCA2 | c.4964dup (p.Tyr1655Ter) c.4595dup (p.Tyr1532Ter) n.4964dup | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32339319_32339320delinsAC | CA2082817603 | BRCA2 | c.4964_4965delinsAC (p.Tyr1655=) c.4595_4596delinsAC (p.Tyr1532=) n.4964_4965delinsAC | |
| 13 | g.32339320_32339323del | CA2739277588 | BRCA2 | c.4965_4968del (p.Tyr1655Ter) c.4596_4599del (p.Tyr1532Ter) n.4965_4968del | ClinVar |
| 13 | g.32339320del | CA021074 | BRCA2 | c.4965del (p.Tyr1655Ter) c.4596del (p.Tyr1532Ter) n.4965del | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339320C>A | CA021066 | BRCA2 | c.4965C>A (p.Tyr1655Ter) c.4596C>A (p.Tyr1532Ter) n.4965C>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339320C= | CA2082817613 | BRCA2 | c.4965C= (p.Tyr1655=) c.4596C= (p.Tyr1532=) n.4965C= | |
| 13 | g.32339320C>G | CA021070 | BRCA2 | c.4965C>G (p.Tyr1655Ter) c.4596C>G (p.Tyr1532Ter) n.4965C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32339320C>T | CA483438290 | BRCA2 | c.4965C>T (p.Tyr1655=) c.4596C>T (p.Tyr1532=) n.4965C>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339320delinsGA | CA10586531 | BRCA2 | c.4965delinsGA (p.Tyr1655Ter) c.4596delinsGA (p.Tyr1532Ter) n.4965delinsGA | ClinVar dbSNP |
| 13 | g.32339321A= | CA2082817623 | BRCA2 | c.4966A= (p.Thr1656=) c.4597A= (p.Thr1533=) n.4966A= | |
| 13 | g.32339321A>C | CA6940835 | BRCA2 | c.4966A>C (p.Thr1656Pro) c.4597A>C (p.Thr1533Pro) n.4966A>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32339321A>G | CA387783809 | BRCA2 | c.4966A>G (p.Thr1656Ala) c.4597A>G (p.Thr1533Ala) n.4966A>G | dbSNP |
| 13 | g.32339321A>T | CA387783811 | BRCA2 | c.4966A>T (p.Thr1656Ser) c.4597A>T (p.Thr1533Ser) n.4966A>T | dbSNP |
| 13 | g.32339322C>A | CA387783813 | BRCA2 | c.4967C>A (p.Thr1656Lys) c.4598C>A (p.Thr1533Lys) n.4967C>A | |
| 13 | g.32339322C= | CA2082817630 | BRCA2 | c.4967C= (p.Thr1656=) c.4598C= (p.Thr1533=) n.4967C= | |
| 13 | g.32339322C>G | CA10579641 | BRCA2 | c.4967C>G (p.Thr1656Arg) c.4598C>G (p.Thr1533Arg) n.4967C>G | ClinVar dbSNP |
| 13 | g.32339322C>T | CA387783815 | BRCA2 | c.4967C>T (p.Thr1656Ile) c.4598C>T (p.Thr1533Ile) n.4967C>T | ClinVar dbSNP |
| 13 | g.32339323A= | CA2082817648 | BRCA2 | c.4968A= (p.Thr1656=) c.4599A= (p.Thr1533=) n.4968A= | |
| 13 | g.32339323A>C | CA16613979 | BRCA2 | c.4968A>C (p.Thr1656=) c.4599A>C (p.Thr1533=) n.4968A>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339323A>G | CA16614153 | BRCA2 | c.4968A>G (p.Thr1656=) c.4599A>G (p.Thr1533=) n.4968A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32339323A>T | CA483438293 | BRCA2 | c.4968A>T (p.Thr1656=) c.4599A>T (p.Thr1533=) n.4968A>T | ClinVar dbSNP |
| 13 | g.32339323_32339324insGT | CA2499222183 | BRCA2 | c.4968_4969insGT (p.Asn1657ValfsTer14) c.4599_4600insGT (p.Asn1534ValfsTer14) n.4968_4969insGT | |
| 13 | g.32339323_32339324insCACCACACCCAAACACACCCAACAC | CA2798720054 | BRCA2 | c.4968_4969insCACCACACCCAAACACACCCAACAC (p.Asn1657HisfsTer17) c.4599_4600insCACCACACCCAAACACACCCAACAC (p.Asn1534HisfsTer17) n.4968_4969insCACCACACCCAAACACACCCAACAC | |
| 13 | g.32339324A= | CA2082817655 | BRCA2 | c.4969A= (p.Asn1657=) c.4600A= (p.Asn1534=) n.4969A= | |
| 13 | g.32339324A>C | CA021077 | BRCA2 | c.4969A>C (p.Asn1657His) c.4600A>C (p.Asn1534His) n.4969A>C | ClinVar dbSNP |
| 13 | g.32339324A>G | CA021079 | BRCA2 | c.4969A>G (p.Asn1657Asp) c.4600A>G (p.Asn1534Asp) n.4969A>G | ClinVar dbSNP |
| 13 | g.32339324A>T | CA387783818 | BRCA2 | c.4969A>T (p.Asn1657Tyr) c.4600A>T (p.Asn1534Tyr) n.4969A>T | ClinVar dbSNP |
| 13 | g.32339325A= | CA2082817674 | BRCA2 | c.4970A= (p.Asn1657=) c.4601A= (p.Asn1534=) n.4970A= | |
| 13 | g.32339325A>C | CA387783824 | BRCA2 | c.4970A>C (p.Asn1657Thr) c.4601A>C (p.Asn1534Thr) n.4970A>C | ClinVar dbSNP |
| 13 | g.32339325A>G | CA16614154 | BRCA2 | c.4970A>G (p.Asn1657Ser) c.4601A>G (p.Asn1534Ser) n.4970A>G | ClinVar dbSNP |
| 13 | g.32339325A>T | CA387783821 | BRCA2 | c.4970A>T (p.Asn1657Ile) c.4601A>T (p.Asn1534Ile) n.4970A>T | |
| 13 | g.32339326T>A | CA387783827 | BRCA2 | c.4971T>A (p.Asn1657Lys) c.4602T>A (p.Asn1534Lys) n.4971T>A | dbSNP |
| 13 | g.32339326T>C | CA483438295 | BRCA2 | c.4971T>C (p.Asn1657=) c.4602T>C (p.Asn1534=) n.4971T>C | |
| 13 | g.32339326T>G | CA387783825 | BRCA2 | c.4971T>G (p.Asn1657Lys) c.4602T>G (p.Asn1534Lys) n.4971T>G | dbSNP |
| 13 | g.32339327C>A | CA387783831 | BRCA2 | c.4972C>A (p.Gln1658Lys) c.4603C>A (p.Gln1535Lys) n.4972C>A | dbSNP |
| 13 | g.32339327C= | CA2082817683 | BRCA2 | c.4972C= (p.Gln1658=) c.4603C= (p.Gln1535=) n.4972C= | |
| 13 | g.32339327C>G | CA387783830 | BRCA2 | c.4972C>G (p.Gln1658Glu) c.4603C>G (p.Gln1535Glu) n.4972C>G | ClinVar dbSNP |
| 13 | g.32339327C>T | CA10586532 | BRCA2 | c.4972C>T (p.Gln1658Ter) c.4603C>T (p.Gln1535Ter) n.4972C>T | ClinVar dbSNP COSMIC COSMIC |
| 13 | g.32339328A= | CA2082817706 | BRCA2 | c.4973A= (p.Gln1658=) c.4604A= (p.Gln1535=) n.4973A= | |
| 13 | g.32339328A>C | CA387783835 | BRCA2 | c.4973A>C (p.Gln1658Pro) c.4604A>C (p.Gln1535Pro) n.4973A>C | |
| 13 | g.32339328A>G | CA387783837 | BRCA2 | c.4973A>G (p.Gln1658Arg) c.4604A>G (p.Gln1535Arg) n.4973A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339328A>T | CA387783838 | BRCA2 | c.4973A>T (p.Gln1658Leu) c.4604A>T (p.Gln1535Leu) n.4973A>T | dbSNP |
| 13 | g.32339328_32339329delinsAG | CA2082817712 | BRCA2 | c.4973_4974delinsAG (p.Gln1658=) c.4604_4605delinsAG (p.Gln1535=) n.4973_4974delinsAG | |
| 13 | g.32339329del | CA658823625 | BRCA2 | c.4974del (p.Gln1658HisfsTer12) c.4605del (p.Gln1535HisfsTer12) n.4974del | ClinVar dbSNP |
| 13 | g.32339329G>A | CA483438299 | BRCA2 | c.4974G>A (p.Gln1658=) c.4605G>A (p.Gln1535=) n.4974G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339329G>C | CA387783840 | BRCA2 | c.4974G>C (p.Gln1658His) c.4605G>C (p.Gln1535His) n.4974G>C | ClinVar dbSNP |
| 13 | g.32339329G= | CA2082817719 | BRCA2 | c.4974G= (p.Gln1658=) c.4605G= (p.Gln1535=) n.4974G= | |
| 13 | g.32339329G>T | CA387783841 | BRCA2 | c.4974G>T (p.Gln1658His) c.4605G>T (p.Gln1535His) n.4974G>T | ClinVar dbSNP |
| 13 | g.32339330T>A | CA387783843 | BRCA2 | c.4975T>A (p.Ser1659Thr) c.4606T>A (p.Ser1536Thr) n.4975T>A | |
| 13 | g.32339330T>C | CA387783844 | BRCA2 | c.4975T>C (p.Ser1659Pro) c.4606T>C (p.Ser1536Pro) n.4975T>C | gnomAD v4 |
| 13 | g.32339330T>G | CA021085 | BRCA2 | c.4975T>G (p.Ser1659Ala) c.4606T>G (p.Ser1536Ala) n.4975T>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339330T= | CA2082817731 | BRCA2 | c.4975T= (p.Ser1659=) c.4606T= (p.Ser1536=) n.4975T= | |
| 13 | g.32339330_32339331insG | CA658823626 | BRCA2 | c.4975_4976insG (p.Ser1659CysfsTer7) c.4606_4607insG (p.Ser1536CysfsTer7) n.4975_4976insG | ClinVar dbSNP |
| 13 | g.32339331C>A | CA387783847 | BRCA2 | c.4976C>A (p.Ser1659Tyr) c.4607C>A (p.Ser1536Tyr) n.4976C>A | dbSNP |
| 13 | g.32339331C= | CA2082817753 | BRCA2 | c.4976C= (p.Ser1659=) c.4607C= (p.Ser1536=) n.4976C= | |
| 13 | g.32339331C>G | CA387783848 | BRCA2 | c.4976C>G (p.Ser1659Cys) c.4607C>G (p.Ser1536Cys) n.4976C>G | dbSNP |
| 13 | g.32339331C>T | CA387783850 | BRCA2 | c.4976C>T (p.Ser1659Phe) c.4607C>T (p.Ser1536Phe) n.4976C>T | ClinVar dbSNP |
| 13 | g.32339334del | CA2695199696 | BRCA2 | c.4979del (p.Pro1660LeufsTer10) c.4610del (p.Pro1537LeufsTer10) n.4979del | ClinVar |
| 13 | g.32339331_32339332insG | CA021089 | BRCA2 | c.4976_4977insG (p.Tyr1661LeufsTer5) c.4607_4608insG (p.Tyr1538LeufsTer5) n.4976_4977insG | ClinVar dbSNP |
| 13 | g.32339332C>A | CA483438300 | BRCA2 | c.4977C>A (p.Ser1659=) c.4608C>A (p.Ser1536=) n.4977C>A | dbSNP |
| 13 | g.32339332C= | CA2082817763 | BRCA2 | c.4977C= (p.Ser1659=) c.4608C= (p.Ser1536=) n.4977C= | |
| 13 | g.32339332C>G | CA483438301 | BRCA2 | c.4977C>G (p.Ser1659=) c.4608C>G (p.Ser1536=) n.4977C>G | dbSNP |
| 13 | g.32339332C>T | CA021093 | BRCA2 | c.4977C>T (p.Ser1659=) c.4608C>T (p.Ser1536=) n.4977C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32339333C>A | CA387783853 | BRCA2 | c.4978C>A (p.Pro1660Thr) c.4609C>A (p.Pro1537Thr) n.4978C>A | dbSNP |
| 13 | g.32339333C>G | CA387783855 | BRCA2 | c.4978C>G (p.Pro1660Ala) c.4609C>G (p.Pro1537Ala) n.4978C>G | dbSNP |
| 13 | g.32339333C>T | CA387783854 | BRCA2 | c.4978C>T (p.Pro1660Ser) c.4609C>T (p.Pro1537Ser) n.4978C>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339334C>A | CA387783856 | BRCA2 | c.4979C>A (p.Pro1660His) c.4610C>A (p.Pro1537His) n.4979C>A | dbSNP |
| 13 | g.32339334C= | CA2082817777 | BRCA2 | c.4979C= (p.Pro1660=) c.4610C= (p.Pro1537=) n.4979C= | |
| 13 | g.32339334C>G | CA387783857 | BRCA2 | c.4979C>G (p.Pro1660Arg) c.4610C>G (p.Pro1537Arg) n.4979C>G | dbSNP |
| 13 | g.32339334C>T | CA021095 | BRCA2 | c.4979C>T (p.Pro1660Leu) c.4610C>T (p.Pro1537Leu) n.4979C>T | ClinVar dbSNP |
| 13 | g.32339334_32339335del | CA2499222184 | BRCA2 | c.4979_4980del (p.Pro1660LeufsTer5) c.4610_4611del (p.Pro1537LeufsTer5) n.4979_4980del | ClinVar |
| 13 | g.32339334_32339335delinsCT | CA2082817781 | BRCA2 | c.4979_4980delinsCT (p.Pro1660=) c.4610_4611delinsCT (p.Pro1537=) n.4979_4980delinsCT | |
| 13 | g.32339335T>A | CA483438304 | BRCA2 | c.4980T>A (p.Pro1660=) c.4611T>A (p.Pro1537=) n.4980T>A | dbSNP |
| 13 | g.32339335T>C | CA483438306 | BRCA2 | c.4980T>C (p.Pro1660=) c.4611T>C (p.Pro1537=) n.4980T>C | dbSNP |
| 13 | g.32339335T>G | CA483438303 | BRCA2 | c.4980T>G (p.Pro1660=) c.4611T>G (p.Pro1537=) n.4980T>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339335T= | CA2082817792 | BRCA2 | c.4980T= (p.Pro1660=) c.4611T= (p.Pro1537=) n.4980T= | |
| 13 | g.32339335_32339336dup | CA915948478 | BRCA2 | c.4980_4981dup (p.Tyr1661PhefsTer10) c.4611_4612dup (p.Tyr1538PhefsTer10) n.4980_4981dup | ClinVar dbSNP |
| 13 | g.32339336del | CA10589280 | BRCA2 | c.4981del (p.Tyr1661IlefsTer9) c.4612del (p.Tyr1538IlefsTer9) n.4981del | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339337_32339339del | CA2740097656 | BRCA2 | c.4982_4984del (p.Tyr1661del) c.4613_4615del (p.Tyr1538del) n.4982_4984del | ClinVar |
| 13 | g.32339335_32339336insG | CA658823627 | BRCA2 | c.4980_4981insG (p.Tyr1661ValfsTer5) c.4611_4612insG (p.Tyr1538ValfsTer5) n.4980_4981insG | ClinVar dbSNP |
| 13 | g.32339336T>A | CA387783860 | BRCA2 | c.4981T>A (p.Tyr1661Asn) c.4612T>A (p.Tyr1538Asn) n.4981T>A | dbSNP |
| 13 | g.32339336T>C | CA021101 | BRCA2 | c.4981T>C (p.Tyr1661His) c.4612T>C (p.Tyr1538His) n.4981T>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32339336T>G | CA387783862 | BRCA2 | c.4981T>G (p.Tyr1661Asp) c.4612T>G (p.Tyr1538Asp) n.4981T>G | |
| 13 | g.32339336T= | CA2082817802 | BRCA2 | c.4981T= (p.Tyr1661=) c.4612T= (p.Tyr1538=) n.4981T= | |
| 13 | g.32339336_32339337insGAAT | CA2580087320 | BRCA2 | c.4981_4982insGAAT (p.Tyr1661Ter) c.4612_4613insGAAT (p.Tyr1538Ter) n.4981_4982insGAAT | ClinVar |
| 13 | g.32339336_32339340delinsTATTC | CA2082817804 | BRCA2 | c.4981_4985delinsTATTC (p.Tyr1661=) c.4612_4616delinsTATTC (p.Tyr1538=) n.4981_4985delinsTATTC | |
| 13 | g.32339336_32339337insG | CA021098 | BRCA2 | c.4981_4982insG (p.Tyr1661Ter) c.4612_4613insG (p.Tyr1538Ter) n.4981_4982insG | ClinVar dbSNP |
| 13 | g.32339337A= | CA2082817820 | BRCA2 | c.4982A= (p.Tyr1661=) c.4613A= (p.Tyr1538=) n.4982A= | |
| 13 | g.32339337A>C | CA387783865 | BRCA2 | c.4982A>C (p.Tyr1661Ser) c.4613A>C (p.Tyr1538Ser) n.4982A>C | |
| 13 | g.32339337A>G | CA387783866 | BRCA2 | c.4982A>G (p.Tyr1661Cys) c.4613A>G (p.Tyr1538Cys) n.4982A>G | dbSNP |
| 13 | g.32339337A>T | CA247508812 | BRCA2 | c.4982A>T (p.Tyr1661Phe) c.4613A>T (p.Tyr1538Phe) n.4982A>T | ClinVar dbSNP |
| 13 | g.32339338_32339341del | CA915948479 | BRCA2 | c.4983_4986del (p.Tyr1661Ter) c.4614_4617del (p.Tyr1538Ter) n.4983_4986del | ClinVar dbSNP |
| 13 | g.32339338T>A | CA387783868 | BRCA2 | c.4983T>A (p.Tyr1661Ter) c.4614T>A (p.Tyr1538Ter) n.4983T>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339338T>C | CA483438310 | BRCA2 | c.4983T>C (p.Tyr1661=) c.4614T>C (p.Tyr1538=) n.4983T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339338T>G | CA16616709 | BRCA2 | c.4983T>G (p.Tyr1661Ter) c.4614T>G (p.Tyr1538Ter) n.4983T>G | ClinVar dbSNP |
| 13 | g.32339338T= | CA2082817829 | BRCA2 | c.4983T= (p.Tyr1661=) c.4614T= (p.Tyr1538=) n.4983T= | |
| 13 | g.32339338_32339342delinsTTCAG | CA2082817828 | BRCA2 | c.4983_4987delinsTTCAG (p.Tyr1661=) c.4614_4618delinsTTCAG (p.Tyr1538=) n.4983_4987delinsTTCAG | |
| 13 | g.32339339T>A | CA387783871 | BRCA2 | c.4984T>A (p.Ser1662Thr) c.4615T>A (p.Ser1539Thr) n.4984T>A | dbSNP |
| 13 | g.32339339T>C | CA387783872 | BRCA2 | c.4984T>C (p.Ser1662Pro) c.4615T>C (p.Ser1539Pro) n.4984T>C | ClinVar |
| 13 | g.32339339T>G | CA387783874 | BRCA2 | c.4984T>G (p.Ser1662Ala) c.4615T>G (p.Ser1539Ala) n.4984T>G | |
| 13 | g.32339342_32339345del | CA021107 | BRCA2 | c.4987_4990del (p.Val1663LeufsTer6) c.4618_4621del (p.Val1540LeufsTer6) n.4987_4990del | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339340C>A | CA387783877 | BRCA2 | c.4985C>A (p.Ser1662Ter) c.4616C>A (p.Ser1539Ter) n.4985C>A | dbSNP |
| 13 | g.32339340C= | CA2082817855 | BRCA2 | c.4985C= (p.Ser1662=) c.4616C= (p.Ser1539=) n.4985C= | |
| 13 | g.32339340C>G | CA10589281 | BRCA2 | c.4985C>G (p.Ser1662Ter) c.4616C>G (p.Ser1539Ter) n.4985C>G | ClinVar dbSNP |
| 13 | g.32339340C>T | CA387783879 | BRCA2 | c.4985C>T (p.Ser1662Leu) c.4616C>T (p.Ser1539Leu) n.4985C>T | ClinVar dbSNP |
| 13 | g.32339340_32339342delinsCAG | CA2082817850 | BRCA2 | c.4985_4987delinsCAG (p.Ser1662=) c.4616_4618delinsCAG (p.Ser1539=) n.4985_4987delinsCAG | |
| 13 | g.32339341del | CA2739277589 | BRCA2 | c.4986del (p.Val1663SerfsTer7) c.4617del (p.Val1540SerfsTer7) n.4986del | ClinVar |
| 13 | g.32339341A= | CA2082817859 | BRCA2 | c.4986A= (p.Ser1662=) c.4617A= (p.Ser1539=) n.4986A= | |
| 13 | g.32339341A>C | CA021105 | BRCA2 | c.4986A>C (p.Ser1662=) c.4617A>C (p.Ser1539=) n.4986A>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339341A>G | CA483438314 | BRCA2 | c.4986A>G (p.Ser1662=) c.4617A>G (p.Ser1539=) n.4986A>G | ClinVar dbSNP |
| 13 | g.32339341A>T | CA483438313 | BRCA2 | c.4986A>T (p.Ser1662=) c.4617A>T (p.Ser1539=) n.4986A>T | dbSNP |
| 13 | g.32339341_32339342del | CA919242668 | BRCA2 | c.4986_4987del (p.Val1663HisfsTer2) c.4617_4618del (p.Val1540HisfsTer2) n.4986_4987del | dbSNP |
| 13 | g.32339342G>A | CA387783882 | BRCA2 | c.4987G>A (p.Val1663Ile) c.4618G>A (p.Val1540Ile) n.4987G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339342G>C | CA021111 | BRCA2 | c.4987G>C (p.Val1663Leu) c.4618G>C (p.Val1540Leu) n.4987G>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32339342G= | CA2082817892 | BRCA2 | c.4987G= (p.Val1663=) c.4618G= (p.Val1540=) n.4987G= | |
| 13 | g.32339342G>T | CA6940836 | BRCA2 | c.4987G>T (p.Val1663Phe) c.4618G>T (p.Val1540Phe) n.4987G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32339343T>A | CA387783884 | BRCA2 | c.4988T>A (p.Val1663Asp) c.4619T>A (p.Val1540Asp) n.4988T>A | dbSNP |
| 13 | g.32339343T>C | CA16614162 | BRCA2 | c.4988T>C (p.Val1663Ala) c.4619T>C (p.Val1540Ala) n.4988T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339343T>G | CA387783885 | BRCA2 | c.4988T>G (p.Val1663Gly) c.4619T>G (p.Val1540Gly) n.4988T>G | |
| 13 | g.32339343T= | CA2082817902 | BRCA2 | c.4988T= (p.Val1663=) c.4619T= (p.Val1540=) n.4988T= | |
| 13 | g.32339344C>A | CA483438318 | BRCA2 | c.4989C>A (p.Val1663=) c.4620C>A (p.Val1540=) n.4989C>A | dbSNP gnomAD v4 |
| 13 | g.32339344C>G | CA483438319 | BRCA2 | c.4989C>G (p.Val1663=) c.4620C>G (p.Val1540=) n.4989C>G | |
| 13 | g.32339344C>T | CA483438320 | BRCA2 | c.4989C>T (p.Val1663=) c.4620C>T (p.Val1540=) n.4989C>T | dbSNP |
| 13 | g.32339344_32339346delinsCAT | CA2082817909 | BRCA2 | c.4989_4991delinsCAT (p.Val1663=) c.4620_4622delinsCAT (p.Val1540=) n.4989_4991delinsCAT | |
| 13 | g.32339345del | CA2840299320 | BRCA2 | c.4990del (p.Ile1664LeufsTer6) c.4621del (p.Ile1541LeufsTer6) n.4990del | |
| 13 | g.32339345A= | CA2082817917 | BRCA2 | c.4990A= (p.Ile1664=) c.4621A= (p.Ile1541=) n.4990A= | |
| 13 | g.32339345A>C | CA387783887 | BRCA2 | c.4990A>C (p.Ile1664Leu) c.4621A>C (p.Ile1541Leu) n.4990A>C | |
| 13 | g.32339345A>G | CA387783889 | BRCA2 | c.4990A>G (p.Ile1664Val) c.4621A>G (p.Ile1541Val) n.4990A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339345A>T | CA387783888 | BRCA2 | c.4990A>T (p.Ile1664Phe) c.4621A>T (p.Ile1541Phe) n.4990A>T | |
| 13 | g.32339345_32339346del | CA021114 | BRCA2 | c.4990_4991del (p.Ile1664Ter) c.4621_4622del (p.Ile1541Ter) n.4990_4991del | ClinVar dbSNP |
| 13 | g.32339346T>A | CA387783890 | BRCA2 | c.4991T>A (p.Ile1664Asn) c.4622T>A (p.Ile1541Asn) n.4991T>A | dbSNP |
| 13 | g.32339346T>C | CA338267 | BRCA2 | c.4991T>C (p.Ile1664Thr) c.4622T>C (p.Ile1541Thr) n.4991T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339346T>G | CA387783891 | BRCA2 | c.4991T>G (p.Ile1664Ser) c.4622T>G (p.Ile1541Ser) n.4991T>G | |
| 13 | g.32339346T= | CA2082817921 | BRCA2 | c.4991T= (p.Ile1664=) c.4622T= (p.Ile1541=) n.4991T= | |
| 13 | g.32339347T>A | CA483438323 | BRCA2 | c.4992T>A (p.Ile1664=) c.4623T>A (p.Ile1541=) n.4992T>A | dbSNP |
| 13 | g.32339347T>C | CA483438322 | BRCA2 | c.4992T>C (p.Ile1664=) c.4623T>C (p.Ile1541=) n.4992T>C | dbSNP |
| 13 | g.32339347T>G | CA387783892 | BRCA2 | c.4992T>G (p.Ile1664Met) c.4623T>G (p.Ile1541Met) n.4992T>G | |
| 13 | g.32339348G>A | CA387783894 | BRCA2 | c.4993G>A (p.Glu1665Lys) c.4624G>A (p.Glu1542Lys) n.4993G>A | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32339348G>C | CA387783896 | BRCA2 | c.4993G>C (p.Glu1665Gln) c.4624G>C (p.Glu1542Gln) n.4993G>C | ClinVar dbSNP COSMIC |
| 13 | g.32339348G= | CA2082817927 | BRCA2 | c.4993G= (p.Glu1665=) c.4624G= (p.Glu1542=) n.4993G= | |
| 13 | g.32339348G>T | CA387783897 | BRCA2 | c.4993G>T (p.Glu1665Ter) c.4624G>T (p.Glu1542Ter) n.4993G>T | |
| 13 | g.32339349A= | CA2082817938 | BRCA2 | c.4994A= (p.Glu1665=) c.4625A= (p.Glu1542=) n.4994A= | |
| 13 | g.32339349A>C | CA387783898 | BRCA2 | c.4994A>C (p.Glu1665Ala) c.4625A>C (p.Glu1542Ala) n.4994A>C | dbSNP |
| 13 | g.32339349A>G | CA6940837 | BRCA2 | c.4994A>G (p.Glu1665Gly) c.4625A>G (p.Glu1542Gly) n.4994A>G | ClinVar dbSNP ExAC gnomAD v2 |
| 13 | g.32339349A>T | CA387783899 | BRCA2 | c.4994A>T (p.Glu1665Val) c.4625A>T (p.Glu1542Val) n.4994A>T | dbSNP |
| 13 | g.32339352del | CA2580087321 | BRCA2 | c.4997del (p.Asn1666IlefsTer4) c.4628del (p.Asn1543IlefsTer4) n.4997del | ClinVar |
| 13 | g.32339350A>C | CA387783901 | BRCA2 | c.4995A>C (p.Glu1665Asp) c.4626A>C (p.Glu1542Asp) n.4995A>C | |
| 13 | g.32339350A>G | CA483438325 | BRCA2 | c.4995A>G (p.Glu1665=) c.4626A>G (p.Glu1542=) n.4995A>G | dbSNP |
| 13 | g.32339350A>T | CA387783900 | BRCA2 | c.4995A>T (p.Glu1665Asp) c.4626A>T (p.Glu1542Asp) n.4995A>T | dbSNP |
| 13 | g.32339351A= | CA2082817952 | BRCA2 | c.4996A= (p.Asn1666=) c.4627A= (p.Asn1543=) n.4996A= | |
| 13 | g.32339351A>C | CA387783902 | BRCA2 | c.4996A>C (p.Asn1666His) c.4627A>C (p.Asn1543His) n.4996A>C | |
| 13 | g.32339351A>G | CA6940838 | BRCA2 | c.4996A>G (p.Asn1666Asp) c.4627A>G (p.Asn1543Asp) n.4996A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32339351A>T | CA387783904 | BRCA2 | c.4996A>T (p.Asn1666Tyr) c.4627A>T (p.Asn1543Tyr) n.4996A>T | dbSNP |
| 13 | g.32339352A= | CA2082817956 | BRCA2 | c.4997A= (p.Asn1666=) c.4628A= (p.Asn1543=) n.4997A= | |
| 13 | g.32339352A>C | CA387783906 | BRCA2 | c.4997A>C (p.Asn1666Thr) c.4628A>C (p.Asn1543Thr) n.4997A>C | dbSNP |
| 13 | g.32339352A>G | CA387783908 | BRCA2 | c.4997A>G (p.Asn1666Ser) c.4628A>G (p.Asn1543Ser) n.4997A>G | ClinVar dbSNP |
| 13 | g.32339352A>T | CA387783910 | BRCA2 | c.4997A>T (p.Asn1666Ile) c.4628A>T (p.Asn1543Ile) n.4997A>T | dbSNP |
| 13 | g.32339353T>A | CA387783911 | BRCA2 | c.4998T>A (p.Asn1666Lys) c.4629T>A (p.Asn1543Lys) n.4998T>A | dbSNP |
| 13 | g.32339353T>C | CA483438327 | BRCA2 | c.4998T>C (p.Asn1666=) c.4629T>C (p.Asn1543=) n.4998T>C | dbSNP gnomAD v4 |
| 13 | g.32339353T>G | CA387783913 | BRCA2 | c.4998T>G (p.Asn1666Lys) c.4629T>G (p.Asn1543Lys) n.4998T>G | |
| 13 | g.32339354dup | CA021117 | BRCA2 | c.4999dup (p.Ser1667PhefsTer10) c.4630dup (p.Ser1544PhefsTer10) n.4999dup | ClinVar dbSNP |
| 13 | g.32339354T>A | CA387783914 | BRCA2 | c.4999T>A (p.Ser1667Thr) c.4630T>A (p.Ser1544Thr) n.4999T>A | ClinVar dbSNP |
| 13 | g.32339354T>C | CA387783917 | BRCA2 | c.4999T>C (p.Ser1667Pro) c.4630T>C (p.Ser1544Pro) n.4999T>C | dbSNP |
| 13 | g.32339354T>G | CA387783916 | BRCA2 | c.4999T>G (p.Ser1667Ala) c.4630T>G (p.Ser1544Ala) n.4999T>G | |
| 13 | g.32339355C>A | CA387783919 | BRCA2 | c.5000C>A (p.Ser1667Ter) c.4631C>A (p.Ser1544Ter) n.5000C>A | dbSNP |
| 13 | g.32339355C= | CA2082817965 | BRCA2 | c.5000C= (p.Ser1667=) c.4631C= (p.Ser1544=) n.5000C= | |
| 13 | g.32339355C>G | CA021122 | BRCA2 | c.5000C>G (p.Ser1667Ter) c.4631C>G (p.Ser1544Ter) n.5000C>G | ClinVar dbSNP |
| 13 | g.32339355C>T | CA387783921 | BRCA2 | c.5000C>T (p.Ser1667Leu) c.4631C>T (p.Ser1544Leu) n.5000C>T | ClinVar dbSNP |
| 13 | g.32339356A= | CA2082817985 | BRCA2 | c.5001A= (p.Ser1667=) c.4632A= (p.Ser1544=) n.5001A= | |
| 13 | g.32339356A>C | CA247508843 | BRCA2 | c.5001A>C (p.Ser1667=) c.4632A>C (p.Ser1544=) n.5001A>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339356A>G | CA483438330 | BRCA2 | c.5001A>G (p.Ser1667=) c.4632A>G (p.Ser1544=) n.5001A>G | dbSNP gnomAD v4 |
| 13 | g.32339356A>T | CA483438331 | BRCA2 | c.5001A>T (p.Ser1667=) c.4632A>T (p.Ser1544=) n.5001A>T | dbSNP |
| 13 | g.32339357G>A | CA021125 | BRCA2 | c.5002G>A (p.Ala1668Thr) c.4633G>A (p.Ala1545Thr) n.5002G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32339357G>C | CA10583110 | BRCA2 | c.5002G>C (p.Ala1668Pro) c.4633G>C (p.Ala1545Pro) n.5002G>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339357G= | CA2082817998 | BRCA2 | c.5002G= (p.Ala1668=) c.4633G= (p.Ala1545=) n.5002G= | |
| 13 | g.32339357G>T | CA387783924 | BRCA2 | c.5002G>T (p.Ala1668Ser) c.4633G>T (p.Ala1545Ser) n.5002G>T | dbSNP |
| 13 | g.32339358C>A | CA387783926 | BRCA2 | c.5003C>A (p.Ala1668Asp) c.4634C>A (p.Ala1545Asp) n.5003C>A | dbSNP |
| 13 | g.32339358C= | CA2082818007 | BRCA2 | c.5003C= (p.Ala1668=) c.4634C= (p.Ala1545=) n.5003C= | |
| 13 | g.32339358C>G | CA021128 | BRCA2 | c.5003C>G (p.Ala1668Gly) c.4634C>G (p.Ala1545Gly) n.5003C>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339358C>T | CA387783929 | BRCA2 | c.5003C>T (p.Ala1668Val) c.4634C>T (p.Ala1545Val) n.5003C>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339359del | CA2843744728 | BRCA2 | c.5004del (p.Leu1669Ter) c.4635del (p.Leu1546Ter) n.5004del | |
| 13 | g.32339359C>A | CA483438335 | BRCA2 | c.5004C>A (p.Ala1668=) c.4635C>A (p.Ala1545=) n.5004C>A | dbSNP gnomAD v4 |
| 13 | g.32339359C= | CA2082818014 | BRCA2 | c.5004C= (p.Ala1668=) c.4635C= (p.Ala1545=) n.5004C= | |
| 13 | g.32339359C>G | CA483438336 | BRCA2 | c.5004C>G (p.Ala1668=) c.4635C>G (p.Ala1545=) n.5004C>G | ClinVar dbSNP |
| 13 | g.32339359C>T | CA483438337 | BRCA2 | c.5004C>T (p.Ala1668=) c.4635C>T (p.Ala1545=) n.5004C>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339359_32339360delinsCT | CA2082818038 | BRCA2 | c.5004_5005delinsCT (p.Ala1668=) c.4635_4636delinsCT (p.Ala1545=) n.5004_5005delinsCT | |
| 13 | g.32339360T>A | CA6940839 | BRCA2 | c.5005T>A (p.Leu1669Ile) c.4636T>A (p.Leu1546Ile) n.5005T>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32339360T>C | CA483438342 | BRCA2 | c.5005T>C (p.Leu1669=) c.4636T>C (p.Leu1546=) n.5005T>C | dbSNP |
| 13 | g.32339360T>G | CA387783930 | BRCA2 | c.5005T>G (p.Leu1669Val) c.4636T>G (p.Leu1546Val) n.5005T>G | |
| 13 | g.32339360T= | CA2082818053 | BRCA2 | c.5005T= (p.Leu1669=) c.4636T= (p.Leu1546=) n.5005T= | |
| 13 | g.32339361del | CA915948480 | BRCA2 | c.5006del (p.Leu1669Ter) c.4637del (p.Leu1546Ter) n.5006del | ClinVar dbSNP |
| 13 | g.32339361T>A | CA387783931 | BRCA2 | c.5006T>A (p.Leu1669Ter) c.4637T>A (p.Leu1546Ter) n.5006T>A | dbSNP |
| 13 | g.32339361T>C | CA387783932 | BRCA2 | c.5006T>C (p.Leu1669Ser) c.4637T>C (p.Leu1546Ser) n.5006T>C | dbSNP |
| 13 | g.32339361T>G | CA387783933 | BRCA2 | c.5006T>G (p.Leu1669Ter) c.4637T>G (p.Leu1546Ter) n.5006T>G | ClinVar dbSNP |
| 13 | g.32339361T= | CA2082818065 | BRCA2 | c.5006T= (p.Leu1669=) c.4637T= (p.Leu1546=) n.5006T= | |
| 13 | g.32339362A= | CA2082818070 | BRCA2 | c.5007A= (p.Leu1669=) c.4638A= (p.Leu1546=) n.5007A= | |
| 13 | g.32339362A>C | CA387783934 | BRCA2 | c.5007A>C (p.Leu1669Phe) c.4638A>C (p.Leu1546Phe) n.5007A>C | |
| 13 | g.32339362A>G | CA483438343 | BRCA2 | c.5007A>G (p.Leu1669=) c.4638A>G (p.Leu1546=) n.5007A>G | |
| 13 | g.32339362A>T | CA387783935 | BRCA2 | c.5007A>T (p.Leu1669Phe) c.4638A>T (p.Leu1546Phe) n.5007A>T | ClinVar dbSNP |
| 13 | g.32339363G>A | CA387783936 | BRCA2 | c.5008G>A (p.Ala1670Thr) c.4639G>A (p.Ala1547Thr) n.5008G>A | |
| 13 | g.32339363G>C | CA387783937 | BRCA2 | c.5008G>C (p.Ala1670Pro) c.4639G>C (p.Ala1547Pro) n.5008G>C | |
| 13 | g.32339363G>T | CA387783938 | BRCA2 | c.5008G>T (p.Ala1670Ser) c.4639G>T (p.Ala1547Ser) n.5008G>T | dbSNP |
| 13 | g.32339364C>A | CA387783939 | BRCA2 | c.5009C>A (p.Ala1670Asp) c.4640C>A (p.Ala1547Asp) n.5009C>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339364C= | CA2082818081 | BRCA2 | c.5009C= (p.Ala1670=) c.4640C= (p.Ala1547=) n.5009C= | |
| 13 | g.32339364C>G | CA387783941 | BRCA2 | c.5009C>G (p.Ala1670Gly) c.4640C>G (p.Ala1547Gly) n.5009C>G | |
| 13 | g.32339364C>T | CA387783940 | BRCA2 | c.5009C>T (p.Ala1670Val) c.4640C>T (p.Ala1547Val) n.5009C>T | ClinVar dbSNP |
| 13 | g.32339365T>A | CA483438345 | BRCA2 | c.5010T>A (p.Ala1670=) c.4641T>A (p.Ala1547=) n.5010T>A | ClinVar dbSNP |
| 13 | g.32339365T>C | CA483438346 | BRCA2 | c.5010T>C (p.Ala1670=) c.4641T>C (p.Ala1547=) n.5010T>C | |
| 13 | g.32339365T>G | CA16606792 | BRCA2 | c.5010T>G (p.Ala1670=) c.4641T>G (p.Ala1547=) n.5010T>G | ClinVar dbSNP COSMIC COSMIC |
| 13 | g.32339365T= | CA2082818102 | BRCA2 | c.5010T= (p.Ala1670=) c.4641T= (p.Ala1547=) n.5010T= | |
| 13 | g.32339369dup | CA021132 | BRCA2 | c.5014dup (p.Tyr1672LeufsTer5) c.4645dup (p.Tyr1549LeufsTer5) n.5014dup | ClinVar dbSNP |
| 13 | g.32339366T>A | CA387783942 | BRCA2 | c.5011T>A (p.Phe1671Ile) c.4642T>A (p.Phe1548Ile) n.5011T>A | |
| 13 | g.32339366T>C | CA387783943 | BRCA2 | c.5011T>C (p.Phe1671Leu) c.4642T>C (p.Phe1548Leu) n.5011T>C | |
| 13 | g.32339366T>G | CA387783944 | BRCA2 | c.5011T>G (p.Phe1671Val) c.4642T>G (p.Phe1548Val) n.5011T>G | ClinVar dbSNP |
| 13 | g.32339366T= | CA2082818113 | BRCA2 | c.5011T= (p.Phe1671=) c.4642T= (p.Phe1548=) n.5011T= | |
| 13 | g.32339367T>A | CA387783945 | BRCA2 | c.5012T>A (p.Phe1671Tyr) c.4643T>A (p.Phe1548Tyr) n.5012T>A | dbSNP |
| 13 | g.32339367T>C | CA387783946 | BRCA2 | c.5012T>C (p.Phe1671Ser) c.4643T>C (p.Phe1548Ser) n.5012T>C | dbSNP |
| 13 | g.32339367T>G | CA387783947 | BRCA2 | c.5012T>G (p.Phe1671Cys) c.4643T>G (p.Phe1548Cys) n.5012T>G | |
| 13 | g.32339368T>A | CA387783948 | BRCA2 | c.5013T>A (p.Phe1671Leu) c.4644T>A (p.Phe1548Leu) n.5013T>A | dbSNP |
| 13 | g.32339368T>C | CA483438348 | BRCA2 | c.5013T>C (p.Phe1671=) c.4644T>C (p.Phe1548=) n.5013T>C | |
| 13 | g.32339368T>G | CA387783949 | BRCA2 | c.5013T>G (p.Phe1671Leu) c.4644T>G (p.Phe1548Leu) n.5013T>G | |
| 13 | g.32339369T>A | CA387783950 | BRCA2 | c.5014T>A (p.Tyr1672Asn) c.4645T>A (p.Tyr1549Asn) n.5014T>A | dbSNP |
| 13 | g.32339369T>C | CA6940840 | BRCA2 | c.5014T>C (p.Tyr1672His) c.4645T>C (p.Tyr1549His) n.5014T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32339369T>G | CA387783951 | BRCA2 | c.5014T>G (p.Tyr1672Asp) c.4645T>G (p.Tyr1549Asp) n.5014T>G | |
| 13 | g.32339369T= | CA2082818118 | BRCA2 | c.5014T= (p.Tyr1672=) c.4645T= (p.Tyr1549=) n.5014T= | |
| 13 | g.32339370A= | CA2082818136 | BRCA2 | c.5015A= (p.Tyr1672=) c.4646A= (p.Tyr1549=) n.5015A= | |
| 13 | g.32339370A>C | CA387783952 | BRCA2 | c.5015A>C (p.Tyr1672Ser) c.4646A>C (p.Tyr1549Ser) n.5015A>C | dbSNP |
| 13 | g.32339370A>G | CA387783953 | BRCA2 | c.5015A>G (p.Tyr1672Cys) c.4646A>G (p.Tyr1549Cys) n.5015A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339370A>T | CA387783954 | BRCA2 | c.5015A>T (p.Tyr1672Phe) c.4646A>T (p.Tyr1549Phe) n.5015A>T | dbSNP |
| 13 | g.32339371C>A | CA387783955 | BRCA2 | c.5016C>A (p.Tyr1672Ter) c.4647C>A (p.Tyr1549Ter) n.5016C>A | |
| 13 | g.32339371C= | CA2082818137 | BRCA2 | c.5016C= (p.Tyr1672=) c.4647C= (p.Tyr1549=) n.5016C= | |
| 13 | g.32339371C>G | CA348640 | BRCA2 | c.5016C>G (p.Tyr1672Ter) c.4647C>G (p.Tyr1549Ter) n.5016C>G | ClinVar dbSNP |
| 13 | g.32339371C>T | CA483438353 | BRCA2 | c.5016C>T (p.Tyr1672=) c.4647C>T (p.Tyr1549=) n.5016C>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339372A= | CA2082818146 | BRCA2 | c.5017A= (p.Thr1673=) c.4648A= (p.Thr1550=) n.5017A= | |
| 13 | g.32339372A>C | CA387783956 | BRCA2 | c.5017A>C (p.Thr1673Pro) c.4648A>C (p.Thr1550Pro) n.5017A>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339372A>G | CA387783957 | BRCA2 | c.5017A>G (p.Thr1673Ala) c.4648A>G (p.Thr1550Ala) n.5017A>G | dbSNP gnomAD v4 |
| 13 | g.32339372A>T | CA6940841 | BRCA2 | c.5017A>T (p.Thr1673Ser) c.4648A>T (p.Thr1550Ser) n.5017A>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32339372dup | CA915948481 | BRCA2 | c.5017dup (p.Thr1673AsnfsTer4) c.4648dup (p.Thr1550AsnfsTer4) n.5017dup | ClinVar dbSNP |
| 13 | g.32339373C>A | CA387783958 | BRCA2 | c.5018C>A (p.Thr1673Lys) c.4649C>A (p.Thr1550Lys) n.5018C>A | dbSNP |
| 13 | g.32339373C= | CA2082818156 | BRCA2 | c.5018C= (p.Thr1673=) c.4649C= (p.Thr1550=) n.5018C= | |
| 13 | g.32339373C>G | CA387783959 | BRCA2 | c.5018C>G (p.Thr1673Arg) c.4649C>G (p.Thr1550Arg) n.5018C>G | dbSNP |
| 13 | g.32339373C>T | CA247508871 | BRCA2 | c.5018C>T (p.Thr1673Ile) c.4649C>T (p.Thr1550Ile) n.5018C>T | ClinVar dbSNP gnomAD v4 |