Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.32339554_32340264delCA2580087342BRCA2c.5199_5909del (p.Glu1734_Ser1970del)
c.4830_5540del (p.Glu1611_Ser1847del)
n.5199_5909del
ClinVar
13g.32340106_32340965delCA645585173BRCA2c.5751_6610del (p.His1918CysfsTer20)
c.5382_6241del (p.His1795CysfsTer20)
n.5751_6610del
COSMIC COSMIC
13g.32340161_32340171delinsATGTCTGGATTCA2082827776BRCA2c.5806_5816delinsATGTCTGGATT (p.Met1936=)
c.5437_5447delinsATGTCTGGATT (p.Met1813=)
n.5806_5816delinsATGTCTGGATT
13g.32340162_32340171delinsGTCCA658656404BRCA2c.5807_5816delinsGTC (p.Met1936SerfsTer25)
c.5438_5447delinsGTC (p.Met1813SerfsTer25)
n.5807_5816delinsGTC
ClinVar dbSNP
13g.32340164_32340169delinsTCTGGACA2082827831BRCA2c.5809_5814delinsTCTGGA (p.Ser1937=)
c.5440_5445delinsTCTGGA (p.Ser1814=)
n.5809_5814delinsTCTGGA
13g.32340165_32340169delCA919242570BRCA2c.5810_5814del (p.Ser1937PhefsTer6)
c.5441_5445del (p.Ser1814PhefsTer6)
n.5810_5814del
dbSNP gnomAD v4
13g.32340169_32340172delCA1139770796BRCA2c.5814_5817del (p.Leu1939ArgfsTer23)
c.5445_5448del (p.Leu1816ArgfsTer23)
n.5814_5817del
13g.32340169A>CCA483438975BRCA2c.5814A>C (p.Gly1938=)
c.5445A>C (p.Gly1815=)
n.5814A>C
13g.32340169A>GCA483438976BRCA2c.5814A>G (p.Gly1938=)
c.5445A>G (p.Gly1815=)
n.5814A>G
dbSNP
13g.32340169A>TCA483438974BRCA2c.5814A>T (p.Gly1938=)
c.5445A>T (p.Gly1815=)
n.5814A>T
ClinVar dbSNP
13g.32340170T>ACA387787262BRCA2c.5815T>A (p.Leu1939Met)
c.5446T>A (p.Leu1816Met)
n.5815T>A
ClinVar dbSNP
13g.32340170T>CCA483438977BRCA2c.5815T>C (p.Leu1939=)
c.5446T>C (p.Leu1816=)
n.5815T>C
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32340170T>GCA387787264BRCA2c.5815T>G (p.Leu1939Val)
c.5446T>G (p.Leu1816Val)
n.5815T>G
dbSNP
13g.32340170T=CA2082827865BRCA2c.5815T= (p.Leu1939=)
c.5446T= (p.Leu1816=)
n.5815T=
13g.32340171T>ACA387787266BRCA2c.5816T>A (p.Leu1939Ter)
c.5447T>A (p.Leu1816Ter)
n.5816T>A
ClinVar dbSNP
13g.32340171T>CCA387787269BRCA2c.5816T>C (p.Leu1939Ser)
c.5447T>C (p.Leu1816Ser)
n.5816T>C
ClinVar gnomAD v4
13g.32340171T>GCA387787267BRCA2c.5816T>G (p.Leu1939Trp)
c.5447T>G (p.Leu1816Trp)
n.5816T>G
13g.32340171T=CA2082827871BRCA2c.5816T= (p.Leu1939=)
c.5447T= (p.Leu1816=)
n.5816T=
13g.32340172G>ACA483438978BRCA2c.5817G>A (p.Leu1939=)
c.5448G>A (p.Leu1816=)
n.5817G>A
ClinVar dbSNP gnomAD v4
13g.32340172G>CCA387787270BRCA2c.5817G>C (p.Leu1939Phe)
c.5448G>C (p.Leu1816Phe)
n.5817G>C
dbSNP
13g.32340172G>TCA387787272BRCA2c.5817G>T (p.Leu1939Phe)
c.5448G>T (p.Leu1816Phe)
n.5817G>T
dbSNP
13g.32340172_32340178delinsGGAGAAACA2082827877BRCA2c.5817_5823delinsGGAGAAA (p.Leu1939=)
c.5448_5454delinsGGAGAAA (p.Leu1816=)
n.5817_5823delinsGGAGAAA
13g.32340173G>ACA387787273BRCA2c.5818G>A (p.Glu1940Lys)
c.5449G>A (p.Glu1817Lys)
n.5818G>A
ClinVar
13g.32340173G>CCA387787275BRCA2c.5818G>C (p.Glu1940Gln)
c.5449G>C (p.Glu1817Gln)
n.5818G>C
13g.32340173G=CA2082827889BRCA2c.5818G= (p.Glu1940=)
c.5449G= (p.Glu1817=)
n.5818G=
13g.32340173G>TCA387787277BRCA2c.5818G>T (p.Glu1940Ter)
c.5449G>T (p.Glu1817Ter)
n.5818G>T
ClinVar dbSNP
13g.32340174_32340179delCA919242571BRCA2c.5819_5824del (p.Glu1940_Lys1941del)
c.5450_5455del (p.Glu1817_Lys1818del)
n.5819_5824del
dbSNP gnomAD v4
13g.32340173_32340187delinsGAGAAAGTTTCTAAACA2082827888BRCA2c.5818_5832delinsGAGAAAGTTTCTAAA (p.Glu1940=)
c.5449_5463delinsGAGAAAGTTTCTAAA (p.Glu1817=)
n.5818_5832delinsGAGAAAGTTTCTAAA
13g.32340174A=CA2082827898BRCA2c.5819A= (p.Glu1940=)
c.5450A= (p.Glu1817=)
n.5819A=
13g.32340174A>CCA387787278BRCA2c.5819A>C (p.Glu1940Ala)
c.5450A>C (p.Glu1817Ala)
n.5819A>C
ClinVar dbSNP
13g.32340174A>GCA387787280BRCA2c.5819A>G (p.Glu1940Gly)
c.5450A>G (p.Glu1817Gly)
n.5819A>G
ClinVar dbSNP
13g.32340174A>TCA387787282BRCA2c.5819A>T (p.Glu1940Val)
c.5450A>T (p.Glu1817Val)
n.5819A>T
dbSNP
13g.32340175_32340188delCA023268BRCA2c.5820_5833del (p.Glu1940AspfsTer5)
c.5451_5464del (p.Glu1817AspfsTer5)
n.5820_5833del
ClinVar dbSNP
13g.32340175G>ACA483438980BRCA2c.5820G>A (p.Glu1940=)
c.5451G>A (p.Glu1817=)
n.5820G>A
ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32340175G>CCA387787283BRCA2c.5820G>C (p.Glu1940Asp)
c.5451G>C (p.Glu1817Asp)
n.5820G>C
dbSNP
13g.32340175G=CA2082827908BRCA2c.5820G= (p.Glu1940=)
c.5451G= (p.Glu1817=)
n.5820G=
13g.32340175G>TCA387787284BRCA2c.5820G>T (p.Glu1940Asp)
c.5451G>T (p.Glu1817Asp)
n.5820G>T
dbSNP
13g.32340175_32340176delinsGACA2082827907BRCA2c.5820_5821delinsGA (p.Glu1940=)
c.5451_5452delinsGA (p.Glu1817=)
n.5820_5821delinsGA
13g.32340176A=CA2082827926BRCA2c.5821A= (p.Lys1941=)
c.5452A= (p.Lys1818=)
n.5821A=
13g.32340176A>CCA387787290BRCA2c.5821A>C (p.Lys1941Gln)
c.5452A>C (p.Lys1818Gln)
n.5821A>C
ClinVar dbSNP
13g.32340176A>GCA387787288BRCA2c.5821A>G (p.Lys1941Glu)
c.5452A>G (p.Lys1818Glu)
n.5821A>G
ClinVar dbSNP
13g.32340176A>TCA387787287BRCA2c.5821A>T (p.Lys1941Ter)
c.5452A>T (p.Lys1818Ter)
n.5821A>T
dbSNP
13g.32340178delCA023272BRCA2c.5823del (p.Val1942PhefsTer21)
c.5454del (p.Val1819PhefsTer21)
n.5823del
ClinVar dbSNP
13g.32340177_32340178delCA2580087781BRCA2c.5822_5823del (p.Lys1941SerfsTer3)
c.5453_5454del (p.Lys1818SerfsTer3)
n.5822_5823del
ClinVar
13g.32340177A>CCA387787291BRCA2c.5822A>C (p.Lys1941Thr)
c.5453A>C (p.Lys1818Thr)
n.5822A>C
13g.32340177A>GCA387787292BRCA2c.5822A>G (p.Lys1941Arg)
c.5453A>G (p.Lys1818Arg)
n.5822A>G
13g.32340177A>TCA387787294BRCA2c.5822A>T (p.Lys1941Ile)
c.5453A>T (p.Lys1818Ile)
n.5822A>T
dbSNP
13g.32340178A>CCA387787295BRCA2c.5823A>C (p.Lys1941Asn)
c.5454A>C (p.Lys1818Asn)
n.5823A>C
13g.32340178A>GCA483438982BRCA2c.5823A>G (p.Lys1941=)
c.5454A>G (p.Lys1818=)
n.5823A>G
ClinVar dbSNP gnomAD v4
13g.32340178A>TCA387787297BRCA2c.5823A>T (p.Lys1941Asn)
c.5454A>T (p.Lys1818Asn)
n.5823A>T
dbSNP

Number of alleles fetched