Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.32370402_32380145delCA2581463483BRCA2c.8332_9256del
c.8332_*623del
c.7963_8887del
c.8332_*818del
c.8332_9205del
c.799_1672del
c.8340_9264del
c.897_2134del
c.8236_9160del
13g.32370503_32371631dupCA2580087371BRCA2c.8433_8632+531dup
c.8064_8263+531dup
c.900_1099+531dup
c.8441_8640+531dup
c.998_1197+531dup
c.8337_8536+531dup
 ClinVar
13g.32370905C>ACA2727919713BRCA2c.8488-51C>A (n.8488-51C>A)
c.8119-51C>A (n.8119-51C>A)
c.955-51C>A (n.955-51C>A)
c.8496-51C>A (n.8496-51C>A)
c.1053-51C>A
c.8392-51C>A (n.8392-51C>A)
 dbSNP
13g.32370905C=CA2082815106BRCA2c.8488-51C= (n.8488-51C=)
c.8119-51C= (n.8119-51C=)
c.955-51C= (n.955-51C=)
c.8496-51C= (n.8496-51C=)
c.1053-51C=
c.8392-51C= (n.8392-51C=)
13g.32370905C>GCA2727919828BRCA2c.8488-51C>G (n.8488-51C>G)
c.8119-51C>G (n.8119-51C>G)
c.955-51C>G (n.955-51C>G)
c.8496-51C>G (n.8496-51C>G)
c.1053-51C>G
c.8392-51C>G (n.8392-51C>G)
 dbSNP
13g.32370905C>TCA2727919830BRCA2c.8488-51C>T (n.8488-51C>T)
c.8119-51C>T (n.8119-51C>T)
c.955-51C>T (n.955-51C>T)
c.8496-51C>T (n.8496-51C>T)
c.1053-51C>T
c.8392-51C>T (n.8392-51C>T)
 dbSNP
13g.32370906T>CCA2622601296BRCA2c.8488-50T>C (n.8488-50T>C)
c.8119-50T>C (n.8119-50T>C)
c.955-50T>C (n.955-50T>C)
c.8496-50T>C (n.8496-50T>C)
c.1053-50T>C
c.8392-50T>C (n.8392-50T>C)
 gnomAD v4
13g.32370907dupCA2082815108BRCA2c.8488-49dup (n.8488-49dup)
c.8119-49dup (n.8119-49dup)
c.955-49dup (n.955-49dup)
c.8496-49dup (n.8496-49dup)
c.1053-49dup
c.8392-49dup (n.8392-49dup)
 dbSNP
13g.32370908G>CCA609453996BRCA2c.8488-48G>C (n.8488-48G>C)
c.8119-48G>C (n.8119-48G>C)
c.955-48G>C (n.955-48G>C)
c.8496-48G>C (n.8496-48G>C)
c.1053-48G>C
c.8392-48G>C (n.8392-48G>C)
 dbSNP gnomAD v2 gnomAD v4
13g.32370908G=CA2082815112BRCA2c.8488-48G= (n.8488-48G=)
c.8119-48G= (n.8119-48G=)
c.955-48G= (n.955-48G=)
c.8496-48G= (n.8496-48G=)
c.1053-48G=
c.8392-48G= (n.8392-48G=)
13g.32370908G>TCA2622601297BRCA2c.8488-48G>T (n.8488-48G>T)
c.8119-48G>T (n.8119-48G>T)
c.955-48G>T (n.955-48G>T)
c.8496-48G>T (n.8496-48G>T)
c.1053-48G>T
c.8392-48G>T (n.8392-48G>T)
 gnomAD v4
13g.32370909A>TCA2727919834BRCA2c.8488-47A>T (n.8488-47A>T)
c.8119-47A>T (n.8119-47A>T)
c.955-47A>T (n.955-47A>T)
c.8496-47A>T (n.8496-47A>T)
c.1053-47A>T
c.8392-47A>T (n.8392-47A>T)
 dbSNP
13g.32370910dupCA247483938BRCA2c.8488-46dup (n.8488-46dup)
c.8119-46dup (n.8119-46dup)
c.955-46dup (n.955-46dup)
c.8496-46dup (n.8496-46dup)
c.1053-46dup
c.8392-46dup (n.8392-46dup)
 dbSNP
13g.32370910A=CA2082815123BRCA2c.8488-46A= (n.8488-46A=)
c.8119-46A= (n.8119-46A=)
c.955-46A= (n.955-46A=)
c.8496-46A= (n.8496-46A=)
c.1053-46A=
c.8392-46A= (n.8392-46A=)
13g.32370910A>GCA6941243BRCA2c.8488-46A>G (n.8488-46A>G)
c.8119-46A>G (n.8119-46A>G)
c.955-46A>G (n.955-46A>G)
c.8496-46A>G (n.8496-46A>G)
c.1053-46A>G
c.8392-46A>G (n.8392-46A>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.32370911T>ACA2727919867BRCA2c.8488-45T>A (n.8488-45T>A)
c.8119-45T>A (n.8119-45T>A)
c.955-45T>A (n.955-45T>A)
c.8496-45T>A (n.8496-45T>A)
c.1053-45T>A
c.8392-45T>A (n.8392-45T>A)
 dbSNP
13g.32370911T>CCA2727919837BRCA2c.8488-45T>C (n.8488-45T>C)
c.8119-45T>C (n.8119-45T>C)
c.955-45T>C (n.955-45T>C)
c.8496-45T>C (n.8496-45T>C)
c.1053-45T>C
c.8392-45T>C (n.8392-45T>C)
 dbSNP
13g.32370911_32370912insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCCA2546179077BRCA2c.8488-45_8488-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCC (n.8488-45_8488-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCC)
c.8119-45_8119-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCC (n.8119-45_8119-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCC)
c.955-45_955-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCC (n.955-45_955-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCC)
c.8496-45_8496-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCC (n.8496-45_8496-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCC)
c.1053-45_1053-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCC
c.8392-45_8392-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCC (n.8392-45_8392-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCC)
13g.32370911_32370912insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGGCA2560955526BRCA2c.8488-45_8488-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGG (n.8488-45_8488-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGG)
c.8119-45_8119-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGG (n.8119-45_8119-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGG)
c.955-45_955-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGG (n.955-45_955-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGG)
c.8496-45_8496-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGG (n.8496-45_8496-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGG)
c.1053-45_1053-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGG
c.8392-45_8392-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGG (n.8392-45_8392-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGG)
13g.32370911_32370912insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGGGTTTTTGAGCCA2506011789BRCA2c.8488-45_8488-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGGGTTTTTGAGC (n.8488-45_8488-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGGGTTTTTGAGC)
c.8119-45_8119-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGGGTTTTTGAGC (n.8119-45_8119-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGGGTTTTTGAGC)
c.955-45_955-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGGGTTTTTGAGC (n.955-45_955-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGGGTTTTTGAGC)
c.8496-45_8496-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGGGTTTTTGAGC (n.8496-45_8496-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGGGTTTTTGAGC)
c.1053-45_1053-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGGGTTTTTGAGC
c.8392-45_8392-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGGGTTTTTGAGC (n.8392-45_8392-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGGGTTTTTGAGC)
13g.32370911_32370912insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGGGTTTTTGAGCGTTTTTTGAAAGACA2515086587BRCA2c.8488-45_8488-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGGGTTTTTGAGCGTTTTTTGAAAGA (n.8488-45_8488-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGGGTTTTTGAGCGTTTTTTGAAAGA)
c.8119-45_8119-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGGGTTTTTGAGCGTTTTTTGAAAGA (n.8119-45_8119-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGGGTTTTTGAGCGTTTTTTGAAAGA)
c.955-45_955-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGGGTTTTTGAGCGTTTTTTGAAAGA (n.955-45_955-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGGGTTTTTGAGCGTTTTTTGAAAGA)
c.8496-45_8496-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGGGTTTTTGAGCGTTTTTTGAAAGA (n.8496-45_8496-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGGGTTTTTGAGCGTTTTTTGAAAGA)
c.1053-45_1053-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGGGTTTTTGAGCGTTTTTTGAAAGA
c.8392-45_8392-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGGGTTTTTGAGCGTTTTTTGAAAGA (n.8392-45_8392-44insCACCCTCAAGTAGAGGTTGAATGGGCTATTTTTCCTTGATTTTCCGGGGTTTTTGAGCGTTTTTTGAAAGA)
13g.32370912G>CCA2727919943BRCA2c.8488-44G>C (n.8488-44G>C)
c.8119-44G>C (n.8119-44G>C)
c.955-44G>C (n.955-44G>C)
c.8496-44G>C (n.8496-44G>C)
c.1053-44G>C
c.8392-44G>C (n.8392-44G>C)
 dbSNP
13g.32370912G>TCA2727919942BRCA2c.8488-44G>T (n.8488-44G>T)
c.8119-44G>T (n.8119-44G>T)
c.955-44G>T (n.955-44G>T)
c.8496-44G>T (n.8496-44G>T)
c.1053-44G>T
c.8392-44G>T (n.8392-44G>T)
 dbSNP
13g.32370914T>CCA2575387995BRCA2c.8488-42T>C (n.8488-42T>C)
c.8119-42T>C (n.8119-42T>C)
c.955-42T>C (n.955-42T>C)
c.8496-42T>C (n.8496-42T>C)
c.1053-42T>C
c.8392-42T>C (n.8392-42T>C)
13g.32370914T>GCA2082815126BRCA2c.8488-42T>G (n.8488-42T>G)
c.8119-42T>G (n.8119-42T>G)
c.955-42T>G (n.955-42T>G)
c.8496-42T>G (n.8496-42T>G)
c.1053-42T>G
c.8392-42T>G (n.8392-42T>G)
 dbSNP gnomAD v4
13g.32370914T=CA2082815124BRCA2c.8488-42T= (n.8488-42T=)
c.8119-42T= (n.8119-42T=)
c.955-42T= (n.955-42T=)
c.8496-42T= (n.8496-42T=)
c.1053-42T=
c.8392-42T= (n.8392-42T=)
13g.32370915A=CA2082815127BRCA2c.8488-41A= (n.8488-41A=)
c.8119-41A= (n.8119-41A=)
c.955-41A= (n.955-41A=)
c.8496-41A= (n.8496-41A=)
c.1053-41A=
c.8392-41A= (n.8392-41A=)
13g.32370915A>TCA247483940BRCA2c.8488-41A>T (n.8488-41A>T)
c.8119-41A>T (n.8119-41A>T)
c.955-41A>T (n.955-41A>T)
c.8496-41A>T (n.8496-41A>T)
c.1053-41A>T
c.8392-41A>T (n.8392-41A>T)
 dbSNP
13g.32370915dupCA609453997BRCA2c.8488-41dup (n.8488-41dup)
c.8119-41dup (n.8119-41dup)
c.955-41dup (n.955-41dup)
c.8496-41dup (n.8496-41dup)
c.1053-41dup
c.8392-41dup (n.8392-41dup)
 dbSNP gnomAD v2 gnomAD v4
13g.32370916T>ACA2727878208BRCA2c.8488-40T>A (n.8488-40T>A)
c.8119-40T>A (n.8119-40T>A)
c.955-40T>A (n.955-40T>A)
c.8496-40T>A (n.8496-40T>A)
c.1053-40T>A
c.8392-40T>A (n.8392-40T>A)
 dbSNP
13g.32370916T>CCA954695352BRCA2c.8488-40T>C (n.8488-40T>C)
c.8119-40T>C (n.8119-40T>C)
c.955-40T>C (n.955-40T>C)
c.8496-40T>C (n.8496-40T>C)
c.1053-40T>C
c.8392-40T>C (n.8392-40T>C)
 dbSNP gnomAD v3 gnomAD v4
13g.32370916T=CA2082815131BRCA2c.8488-40T= (n.8488-40T=)
c.8119-40T= (n.8119-40T=)
c.955-40T= (n.955-40T=)
c.8496-40T= (n.8496-40T=)
c.1053-40T=
c.8392-40T= (n.8392-40T=)
13g.32370917A=CA2082815132BRCA2c.8488-39A= (n.8488-39A=)
c.8119-39A= (n.8119-39A=)
c.955-39A= (n.955-39A=)
c.8496-39A= (n.8496-39A=)
c.1053-39A=
c.8392-39A= (n.8392-39A=)
13g.32370917A>GCA2082815134BRCA2c.8488-39A>G (n.8488-39A>G)
c.8119-39A>G (n.8119-39A>G)
c.955-39A>G (n.955-39A>G)
c.8496-39A>G (n.8496-39A>G)
c.1053-39A>G
c.8392-39A>G (n.8392-39A>G)
 dbSNP gnomAD v4
13g.32370918T>CCA2622601298BRCA2c.8488-38T>C (n.8488-38T>C)
c.8119-38T>C (n.8119-38T>C)
c.955-38T>C (n.955-38T>C)
c.8496-38T>C (n.8496-38T>C)
c.1053-38T>C
c.8392-38T>C (n.8392-38T>C)
 gnomAD v4
13g.32370919A=CA2082815136BRCA2c.8488-37A= (n.8488-37A=)
c.8119-37A= (n.8119-37A=)
c.955-37A= (n.955-37A=)
c.8496-37A= (n.8496-37A=)
c.1053-37A=
c.8392-37A= (n.8392-37A=)
13g.32370919A>GCA6941244BRCA2c.8488-37A>G (n.8488-37A>G)
c.8119-37A>G (n.8119-37A>G)
c.955-37A>G (n.955-37A>G)
c.8496-37A>G (n.8496-37A>G)
c.1053-37A>G
c.8392-37A>G (n.8392-37A>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32370919A>TCA609453998BRCA2c.8488-37A>T (n.8488-37A>T)
c.8119-37A>T (n.8119-37A>T)
c.955-37A>T (n.955-37A>T)
c.8496-37A>T (n.8496-37A>T)
c.1053-37A>T
c.8392-37A>T (n.8392-37A>T)
 dbSNP gnomAD v2 gnomAD v4
13g.32370920T>CCA2622601299BRCA2c.8488-36T>C (n.8488-36T>C)
c.8119-36T>C (n.8119-36T>C)
c.955-36T>C (n.955-36T>C)
c.8496-36T>C (n.8496-36T>C)
c.1053-36T>C
c.8392-36T>C (n.8392-36T>C)
 gnomAD v4
13g.32370921G>ACA2622601300BRCA2c.8488-35G>A (n.8488-35G>A)
c.8119-35G>A (n.8119-35G>A)
c.955-35G>A (n.955-35G>A)
c.8496-35G>A (n.8496-35G>A)
c.1053-35G>A
c.8392-35G>A (n.8392-35G>A)
 dbSNP gnomAD v4
13g.32370921G>CCA2727920054BRCA2c.8488-35G>C (n.8488-35G>C)
c.8119-35G>C (n.8119-35G>C)
c.955-35G>C (n.955-35G>C)
c.8496-35G>C (n.8496-35G>C)
c.1053-35G>C
c.8392-35G>C (n.8392-35G>C)
 dbSNP
13g.32370922T>ACA2727920085BRCA2c.8488-34T>A (n.8488-34T>A)
c.8119-34T>A (n.8119-34T>A)
c.955-34T>A (n.955-34T>A)
c.8496-34T>A (n.8496-34T>A)
c.1053-34T>A
c.8392-34T>A (n.8392-34T>A)
 dbSNP
13g.32370923G>ACA2727920117BRCA2c.8488-33G>A (n.8488-33G>A)
c.8119-33G>A (n.8119-33G>A)
c.955-33G>A (n.955-33G>A)
c.8496-33G>A (n.8496-33G>A)
c.1053-33G>A
c.8392-33G>A (n.8392-33G>A)
 dbSNP
13g.32370923G>CCA2727920157BRCA2c.8488-33G>C (n.8488-33G>C)
c.8119-33G>C (n.8119-33G>C)
c.955-33G>C (n.955-33G>C)
c.8496-33G>C (n.8496-33G>C)
c.1053-33G>C
c.8392-33G>C (n.8392-33G>C)
 dbSNP
13g.32370923G>TCA2727920087BRCA2c.8488-33G>T (n.8488-33G>T)
c.8119-33G>T (n.8119-33G>T)
c.955-33G>T (n.955-33G>T)
c.8496-33G>T (n.8496-33G>T)
c.1053-33G>T
c.8392-33G>T (n.8392-33G>T)
 dbSNP
13g.32370924A=CA2082815142BRCA2c.8488-32A= (n.8488-32A=)
c.8119-32A= (n.8119-32A=)
c.955-32A= (n.955-32A=)
c.8496-32A= (n.8496-32A=)
c.1053-32A=
c.8392-32A= (n.8392-32A=)
13g.32370924A>GCA6941245BRCA2c.8488-32A>G (n.8488-32A>G)
c.8119-32A>G (n.8119-32A>G)
c.955-32A>G (n.955-32A>G)
c.8496-32A>G (n.8496-32A>G)
c.1053-32A>G
c.8392-32A>G (n.8392-32A>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.32370924A>TCA2727839890BRCA2c.8488-32A>T (n.8488-32A>T)
c.8119-32A>T (n.8119-32A>T)
c.955-32A>T (n.955-32A>T)
c.8496-32A>T (n.8496-32A>T)
c.1053-32A>T
c.8392-32A>T (n.8392-32A>T)
 dbSNP
13g.32370925delCA2798730080BRCA2c.8488-31del (n.8488-31del)
c.8119-31del (n.8119-31del)
c.955-31del (n.955-31del)
c.8496-31del (n.8496-31del)
c.1053-31del
c.8392-31del (n.8392-31del)
13g.32370925C>ACA2798730079BRCA2c.8488-31C>A (n.8488-31C>A)
c.8119-31C>A (n.8119-31C>A)
c.955-31C>A (n.955-31C>A)
c.8496-31C>A (n.8496-31C>A)
c.1053-31C>A
c.8392-31C>A (n.8392-31C>A)
13g.32370931dupCA2798730081BRCA2c.8488-25dup (n.8488-25dup)
c.8119-25dup (n.8119-25dup)
c.955-25dup (n.955-25dup)
c.8496-25dup (n.8496-25dup)
c.1053-25dup
c.8392-25dup (n.8392-25dup)
13g.32370931delCA2622601301BRCA2c.8488-25del (n.8488-25del)
c.8119-25del (n.8119-25del)
c.955-25del (n.955-25del)
c.8496-25del (n.8496-25del)
c.1053-25del
c.8392-25del (n.8392-25del)
 gnomAD v4
13g.32370926_32370927insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAACA2510345175BRCA2c.8488-30_8488-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAA (n.8488-30_8488-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAA)
c.8119-30_8119-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAA (n.8119-30_8119-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAA)
c.955-30_955-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAA (n.955-30_955-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAA)
c.8496-30_8496-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAA (n.8496-30_8496-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAA)
c.1053-30_1053-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAA
c.8392-30_8392-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAA (n.8392-30_8392-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAA)
13g.32370926_32370927insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGACA2510889559BRCA2c.8488-30_8488-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGA (n.8488-30_8488-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGA)
c.8119-30_8119-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGA (n.8119-30_8119-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGA)
c.955-30_955-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGA (n.955-30_955-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGA)
c.8496-30_8496-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGA (n.8496-30_8496-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGA)
c.1053-30_1053-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGA
c.8392-30_8392-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGA (n.8392-30_8392-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGA)
13g.32370926_32370927insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGATTTCCAAGCCCGGAATATAGACACCCA2569938872BRCA2c.8488-30_8488-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGATTTCCAAGCCCGGAATATAGACACC (n.8488-30_8488-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGATTTCCAAGCCCGGAATATAGACACC)
c.8119-30_8119-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGATTTCCAAGCCCGGAATATAGACACC (n.8119-30_8119-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGATTTCCAAGCCCGGAATATAGACACC)
c.955-30_955-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGATTTCCAAGCCCGGAATATAGACACC (n.955-30_955-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGATTTCCAAGCCCGGAATATAGACACC)
c.8496-30_8496-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGATTTCCAAGCCCGGAATATAGACACC (n.8496-30_8496-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGATTTCCAAGCCCGGAATATAGACACC)
c.1053-30_1053-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGATTTCCAAGCCCGGAATATAGACACC
c.8392-30_8392-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGATTTCCAAGCCCGGAATATAGACACC (n.8392-30_8392-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGATTTCCAAGCCCGGAATATAGACACC)
13g.32370926_32370927insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGGCACCCA2537641276BRCA2c.8488-30_8488-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGGCACC (n.8488-30_8488-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGGCACC)
c.8119-30_8119-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGGCACC (n.8119-30_8119-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGGCACC)
c.955-30_955-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGGCACC (n.955-30_955-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGGCACC)
c.8496-30_8496-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGGCACC (n.8496-30_8496-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGGCACC)
c.1053-30_1053-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGGCACC
c.8392-30_8392-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGGCACC (n.8392-30_8392-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGGCACC)
13g.32370926_32370927insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGAGTGATTTCCAAGCCCGGAATATAGACACCCA2544859255BRCA2c.8488-30_8488-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGAGTGATTTCCAAGCCCGGAATATAGACACC (n.8488-30_8488-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGAGTGATTTCCAAGCCCGGAATATAGACACC)
c.8119-30_8119-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGAGTGATTTCCAAGCCCGGAATATAGACACC (n.8119-30_8119-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGAGTGATTTCCAAGCCCGGAATATAGACACC)
c.955-30_955-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGAGTGATTTCCAAGCCCGGAATATAGACACC (n.955-30_955-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGAGTGATTTCCAAGCCCGGAATATAGACACC)
c.8496-30_8496-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGAGTGATTTCCAAGCCCGGAATATAGACACC (n.8496-30_8496-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGAGTGATTTCCAAGCCCGGAATATAGACACC)
c.1053-30_1053-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGAGTGATTTCCAAGCCCGGAATATAGACACC
c.8392-30_8392-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGAGTGATTTCCAAGCCCGGAATATAGACACC (n.8392-30_8392-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGAGTGATTTCCAAGCCCGGAATATAGACACC)
13g.32370926_32370927insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCACCA2568356809BRCA2c.8488-30_8488-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC (n.8488-30_8488-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC)
c.8119-30_8119-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC (n.8119-30_8119-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC)
c.955-30_955-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC (n.955-30_955-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC)
c.8496-30_8496-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC (n.8496-30_8496-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC)
c.1053-30_1053-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC
c.8392-30_8392-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC (n.8392-30_8392-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAGAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC)
13g.32370926_32370927insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGAGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCACCA2567007893BRCA2c.8488-30_8488-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGAGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC (n.8488-30_8488-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGAGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC)
c.8119-30_8119-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGAGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC (n.8119-30_8119-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGAGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC)
c.955-30_955-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGAGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC (n.955-30_955-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGAGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC)
c.8496-30_8496-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGAGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC (n.8496-30_8496-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGAGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC)
c.1053-30_1053-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGAGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC
c.8392-30_8392-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGAGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC (n.8392-30_8392-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGACCATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGAGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC)
13g.32370926_32370927insACAATCACTTTCAGGGTGAATTGTTGCACTCGAAGACCAATTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCACCA2561262632BRCA2c.8488-30_8488-29insACAATCACTTTCAGGGTGAATTGTTGCACTCGAAGACCAATTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC (n.8488-30_8488-29insACAATCACTTTCAGGGTGAATTGTTGCACTCGAAGACCAATTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC)
c.8119-30_8119-29insACAATCACTTTCAGGGTGAATTGTTGCACTCGAAGACCAATTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC (n.8119-30_8119-29insACAATCACTTTCAGGGTGAATTGTTGCACTCGAAGACCAATTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC)
c.955-30_955-29insACAATCACTTTCAGGGTGAATTGTTGCACTCGAAGACCAATTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC (n.955-30_955-29insACAATCACTTTCAGGGTGAATTGTTGCACTCGAAGACCAATTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC)
c.8496-30_8496-29insACAATCACTTTCAGGGTGAATTGTTGCACTCGAAGACCAATTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC (n.8496-30_8496-29insACAATCACTTTCAGGGTGAATTGTTGCACTCGAAGACCAATTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC)
c.1053-30_1053-29insACAATCACTTTCAGGGTGAATTGTTGCACTCGAAGACCAATTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC
c.8392-30_8392-29insACAATCACTTTCAGGGTGAATTGTTGCACTCGAAGACCAATTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC (n.8392-30_8392-29insACAATCACTTTCAGGGTGAATTGTTGCACTCGAAGACCAATTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC)
13g.32370926_32370927insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGCCTATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCACCA2514589280BRCA2c.8488-30_8488-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGCCTATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC (n.8488-30_8488-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGCCTATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC)
c.8119-30_8119-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGCCTATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC (n.8119-30_8119-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGCCTATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC)
c.955-30_955-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGCCTATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC (n.955-30_955-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGCCTATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC)
c.8496-30_8496-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGCCTATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC (n.8496-30_8496-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGCCTATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC)
c.1053-30_1053-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGCCTATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC
c.8392-30_8392-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGCCTATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC (n.8392-30_8392-29insACAATCACTTTCAGAGTGAATTGTTGCACTCGAAGCCTATTTTCTTCCAAAAACCGCGGAATTCCGGGGCAAAACGGGTGATTTCCAAGCCCGGAATATAGACACCTTTCGCATATTCCAC)
13g.32370927T>CCA2727920161BRCA2c.8488-29T>C (n.8488-29T>C)
c.8119-29T>C (n.8119-29T>C)
c.955-29T>C (n.955-29T>C)
c.8496-29T>C (n.8496-29T>C)
c.1053-29T>C
c.8392-29T>C (n.8392-29T>C)
 dbSNP
13g.32370928T>ACA2727920163BRCA2c.8488-28T>A (n.8488-28T>A)
c.8119-28T>A (n.8119-28T>A)
c.955-28T>A (n.955-28T>A)
c.8496-28T>A (n.8496-28T>A)
c.1053-28T>A
c.8392-28T>A (n.8392-28T>A)
 dbSNP
13g.32370928T>CCA2727920164BRCA2c.8488-28T>C (n.8488-28T>C)
c.8119-28T>C (n.8119-28T>C)
c.955-28T>C (n.955-28T>C)
c.8496-28T>C (n.8496-28T>C)
c.1053-28T>C
c.8392-28T>C (n.8392-28T>C)
 dbSNP
13g.32370929T>CCA2575387996BRCA2c.8488-27T>C (n.8488-27T>C)
c.8119-27T>C (n.8119-27T>C)
c.955-27T>C (n.955-27T>C)
c.8496-27T>C (n.8496-27T>C)
c.1053-27T>C
c.8392-27T>C (n.8392-27T>C)
 dbSNP
13g.32370930T>ACA2727920255BRCA2c.8488-26T>A (n.8488-26T>A)
c.8119-26T>A (n.8119-26T>A)
c.955-26T>A (n.955-26T>A)
c.8496-26T>A (n.8496-26T>A)
c.1053-26T>A
c.8392-26T>A (n.8392-26T>A)
 dbSNP
13g.32370930T>CCA2727920252BRCA2c.8488-26T>C (n.8488-26T>C)
c.8119-26T>C (n.8119-26T>C)
c.955-26T>C (n.955-26T>C)
c.8496-26T>C (n.8496-26T>C)
c.1053-26T>C
c.8392-26T>C (n.8392-26T>C)
 dbSNP
13g.32370931T>CCA2622601302BRCA2c.8488-25T>C (n.8488-25T>C)
c.8119-25T>C (n.8119-25T>C)
c.955-25T>C (n.955-25T>C)
c.8496-25T>C (n.8496-25T>C)
c.1053-25T>C
c.8392-25T>C (n.8392-25T>C)
 gnomAD v4
13g.32370932G>ACA2825002154BRCA2c.8488-24G>A (n.8488-24G>A)
c.8119-24G>A (n.8119-24G>A)
c.955-24G>A (n.955-24G>A)
c.8496-24G>A (n.8496-24G>A)
c.1053-24G>A
c.8392-24G>A (n.8392-24G>A)
 ClinVar
13g.32370933dupCA2727920257BRCA2c.8488-23dup (n.8488-23dup)
c.8119-23dup (n.8119-23dup)
c.955-23dup (n.955-23dup)
c.8496-23dup (n.8496-23dup)
c.1053-23dup
c.8392-23dup (n.8392-23dup)
 dbSNP
13g.32370933G>ACA609453999BRCA2c.8488-23G>A (n.8488-23G>A)
c.8119-23G>A (n.8119-23G>A)
c.955-23G>A (n.955-23G>A)
c.8496-23G>A (n.8496-23G>A)
c.1053-23G>A
c.8392-23G>A (n.8392-23G>A)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32370933G>CCA2727841194BRCA2c.8488-23G>C (n.8488-23G>C)
c.8119-23G>C (n.8119-23G>C)
c.955-23G>C (n.955-23G>C)
c.8496-23G>C (n.8496-23G>C)
c.1053-23G>C
c.8392-23G>C (n.8392-23G>C)
 dbSNP
13g.32370933G=CA2082815149BRCA2c.8488-23G= (n.8488-23G=)
c.8119-23G= (n.8119-23G=)
c.955-23G= (n.955-23G=)
c.8496-23G= (n.8496-23G=)
c.1053-23G=
c.8392-23G= (n.8392-23G=)
13g.32370933G>TCA6941246BRCA2c.8488-23G>T (n.8488-23G>T)
c.8119-23G>T (n.8119-23G>T)
c.955-23G>T (n.955-23G>T)
c.8496-23G>T (n.8496-23G>T)
c.1053-23G>T
c.8392-23G>T (n.8392-23G>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.32370934T>CCA2622601303BRCA2c.8488-22T>C (n.8488-22T>C)
c.8119-22T>C (n.8119-22T>C)
c.955-22T>C (n.955-22T>C)
c.8496-22T>C (n.8496-22T>C)
c.1053-22T>C
c.8392-22T>C (n.8392-22T>C)
 gnomAD v4
13g.32370934T>GCA2727920283BRCA2c.8488-22T>G (n.8488-22T>G)
c.8119-22T>G (n.8119-22T>G)
c.955-22T>G (n.955-22T>G)
c.8496-22T>G (n.8496-22T>G)
c.1053-22T>G
c.8392-22T>G (n.8392-22T>G)
 dbSNP
13g.32370935G>ACA2622601304BRCA2c.8488-21G>A (n.8488-21G>A)
c.8119-21G>A (n.8119-21G>A)
c.955-21G>A (n.955-21G>A)
c.8496-21G>A (n.8496-21G>A)
c.1053-21G>A
c.8392-21G>A (n.8392-21G>A)
 dbSNP gnomAD v4
13g.32370935G>CCA2727920294BRCA2c.8488-21G>C (n.8488-21G>C)
c.8119-21G>C (n.8119-21G>C)
c.955-21G>C (n.955-21G>C)
c.8496-21G>C (n.8496-21G>C)
c.1053-21G>C
c.8392-21G>C (n.8392-21G>C)
 dbSNP
13g.32370935G>TCA2622601305BRCA2c.8488-21G>T (n.8488-21G>T)
c.8119-21G>T (n.8119-21G>T)
c.955-21G>T (n.955-21G>T)
c.8496-21G>T (n.8496-21G>T)
c.1053-21G>T
c.8392-21G>T (n.8392-21G>T)
 gnomAD v4
13g.32370935_32370936delinsGTCA2082815150BRCA2c.8488-21_8488-20delinsGT (n.8488-21_8488-20delinsGT)
c.8119-21_8119-20delinsGT (n.8119-21_8119-20delinsGT)
c.955-21_955-20delinsGT (n.955-21_955-20delinsGT)
c.8496-21_8496-20delinsGT (n.8496-21_8496-20delinsGT)
c.1053-21_1053-20delinsGT
c.8392-21_8392-20delinsGT (n.8392-21_8392-20delinsGT)
13g.32370936delCA913188609BRCA2c.8488-20del (n.8488-20del)
c.8119-20del (n.8119-20del)
c.955-20del (n.955-20del)
c.8496-20del (n.8496-20del)
c.1053-20del
c.8392-20del (n.8392-20del)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32370936T>ACA2727878210BRCA2c.8488-20T>A (n.8488-20T>A)
c.8119-20T>A (n.8119-20T>A)
c.955-20T>A (n.955-20T>A)
c.8496-20T>A (n.8496-20T>A)
c.1053-20T>A
c.8392-20T>A (n.8392-20T>A)
 dbSNP
13g.32370936T>CCA2727878209BRCA2c.8488-20T>C (n.8488-20T>C)
c.8119-20T>C (n.8119-20T>C)
c.955-20T>C (n.955-20T>C)
c.8496-20T>C (n.8496-20T>C)
c.1053-20T>C
c.8392-20T>C (n.8392-20T>C)
 dbSNP
13g.32370936T>GCA915946897BRCA2c.8488-20T>G (n.8488-20T>G)
c.8119-20T>G (n.8119-20T>G)
c.955-20T>G (n.955-20T>G)
c.8496-20T>G (n.8496-20T>G)
c.1053-20T>G
c.8392-20T>G (n.8392-20T>G)
 ClinVar dbSNP
13g.32370936T=CA2082815156BRCA2c.8488-20T= (n.8488-20T=)
c.8119-20T= (n.8119-20T=)
c.955-20T= (n.955-20T=)
c.8496-20T= (n.8496-20T=)
c.1053-20T=
c.8392-20T= (n.8392-20T=)
13g.32370937G>ACA025676BRCA2c.8488-19G>A (n.8488-19G>A)
c.8119-19G>A (n.8119-19G>A)
c.955-19G>A (n.955-19G>A)
c.8496-19G>A (n.8496-19G>A)
c.1053-19G>A
c.8392-19G>A (n.8392-19G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32370937G>CCA2727836601BRCA2c.8488-19G>C (n.8488-19G>C)
c.8119-19G>C (n.8119-19G>C)
c.955-19G>C (n.955-19G>C)
c.8496-19G>C (n.8496-19G>C)
c.1053-19G>C
c.8392-19G>C (n.8392-19G>C)
 dbSNP
13g.32370937G=CA2082815159BRCA2c.8488-19G= (n.8488-19G=)
c.8119-19G= (n.8119-19G=)
c.955-19G= (n.955-19G=)
c.8496-19G= (n.8496-19G=)
c.1053-19G=
c.8392-19G= (n.8392-19G=)
13g.32370938T>ACA2727920316BRCA2c.8488-18T>A (n.8488-18T>A)
c.8119-18T>A (n.8119-18T>A)
c.955-18T>A (n.955-18T>A)
c.8496-18T>A (n.8496-18T>A)
c.1053-18T>A
c.8392-18T>A (n.8392-18T>A)
 dbSNP
13g.32370938T>CCA2573149211BRCA2c.8488-18T>C (n.8488-18T>C)
c.8119-18T>C (n.8119-18T>C)
c.955-18T>C (n.955-18T>C)
c.8496-18T>C (n.8496-18T>C)
c.1053-18T>C
c.8392-18T>C (n.8392-18T>C)
 ClinVar dbSNP gnomAD v4
13g.32370938T>GCA2727920333BRCA2c.8488-18T>G (n.8488-18T>G)
c.8119-18T>G (n.8119-18T>G)
c.955-18T>G (n.955-18T>G)
c.8496-18T>G (n.8496-18T>G)
c.1053-18T>G
c.8392-18T>G (n.8392-18T>G)
 dbSNP
13g.32370939G>ACA2082815173BRCA2c.8488-17G>A (n.8488-17G>A)
c.8119-17G>A (n.8119-17G>A)
c.955-17G>A (n.955-17G>A)
c.8496-17G>A (n.8496-17G>A)
c.1053-17G>A
c.8392-17G>A (n.8392-17G>A)
 dbSNP
13g.32370939G>CCA2727874237BRCA2c.8488-17G>C (n.8488-17G>C)
c.8119-17G>C (n.8119-17G>C)
c.955-17G>C (n.955-17G>C)
c.8496-17G>C (n.8496-17G>C)
c.1053-17G>C
c.8392-17G>C (n.8392-17G>C)
 dbSNP
13g.32370939G=CA2082815164BRCA2c.8488-17G= (n.8488-17G=)
c.8119-17G= (n.8119-17G=)
c.955-17G= (n.955-17G=)
c.8496-17G= (n.8496-17G=)
c.1053-17G=
c.8392-17G= (n.8392-17G=)
13g.32370939G>TCA2622601306BRCA2c.8488-17G>T (n.8488-17G>T)
c.8119-17G>T (n.8119-17G>T)
c.955-17G>T (n.955-17G>T)
c.8496-17G>T (n.8496-17G>T)
c.1053-17G>T
c.8392-17G>T (n.8392-17G>T)
 gnomAD v4
13g.32370940T>CCA6941247BRCA2c.8488-16T>C (n.8488-16T>C)
c.8119-16T>C (n.8119-16T>C)
c.955-16T>C (n.955-16T>C)
c.8496-16T>C (n.8496-16T>C)
c.1053-16T>C
c.8392-16T>C (n.8392-16T>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32370940T=CA2082815175BRCA2c.8488-16T= (n.8488-16T=)
c.8119-16T= (n.8119-16T=)
c.955-16T= (n.955-16T=)
c.8496-16T= (n.8496-16T=)
c.1053-16T=
c.8392-16T= (n.8392-16T=)
13g.32370941A=CA2082815181BRCA2c.8488-15A= (n.8488-15A=)
c.8119-15A= (n.8119-15A=)
c.955-15A= (n.955-15A=)
c.8496-15A= (n.8496-15A=)
c.1053-15A=
c.8392-15A= (n.8392-15A=)
13g.32370941A>GCA6941248BRCA2c.8488-15A>G (n.8488-15A>G)
c.8119-15A>G (n.8119-15A>G)
c.955-15A>G (n.955-15A>G)
c.8496-15A>G (n.8496-15A>G)
c.1053-15A>G
c.8392-15A>G (n.8392-15A>G)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32370941A>TCA2622601307BRCA2c.8488-15A>T (n.8488-15A>T)
c.8119-15A>T (n.8119-15A>T)
c.955-15A>T (n.955-15A>T)
c.8496-15A>T (n.8496-15A>T)
c.1053-15A>T
c.8392-15A>T (n.8392-15A>T)
 dbSNP gnomAD v4
13g.32370942A=CA2082815183BRCA2c.8488-14A= (n.8488-14A=)
c.8119-14A= (n.8119-14A=)
c.955-14A= (n.955-14A=)
c.8496-14A= (n.8496-14A=)
c.1053-14A=
c.8392-14A= (n.8392-14A=)
13g.32370942A>CCA658656378BRCA2c.8488-14A>C (n.8488-14A>C)
c.8119-14A>C (n.8119-14A>C)
c.955-14A>C (n.955-14A>C)
c.8496-14A>C (n.8496-14A>C)
c.1053-14A>C
c.8392-14A>C (n.8392-14A>C)
 ClinVar dbSNP
13g.32370942A>GCA2082815184BRCA2c.8488-14A>G (n.8488-14A>G)
c.8119-14A>G (n.8119-14A>G)
c.955-14A>G (n.955-14A>G)
c.8496-14A>G (n.8496-14A>G)
c.1053-14A>G
c.8392-14A>G (n.8392-14A>G)
 ClinVar dbSNP gnomAD v4
13g.32370942A>TCA658683832BRCA2c.8488-14A>T (n.8488-14A>T)
c.8119-14A>T (n.8119-14A>T)
c.955-14A>T (n.955-14A>T)
c.8496-14A>T (n.8496-14A>T)
c.1053-14A>T
c.8392-14A>T (n.8392-14A>T)
 ClinVar dbSNP
13g.32370943C>GCA2727920335BRCA2c.8488-13C>G (n.8488-13C>G)
c.8119-13C>G (n.8119-13C>G)
c.955-13C>G (n.955-13C>G)
c.8496-13C>G (n.8496-13C>G)
c.1053-13C>G
c.8392-13C>G (n.8392-13C>G)
 dbSNP
13g.32370943C>TCA2727920334BRCA2c.8488-13C>T (n.8488-13C>T)
c.8119-13C>T (n.8119-13C>T)
c.955-13C>T (n.955-13C>T)
c.8496-13C>T (n.8496-13C>T)
c.1053-13C>T
c.8392-13C>T (n.8392-13C>T)
 dbSNP
13g.32370944A=CA2082815185BRCA2c.8488-12A= (n.8488-12A=)
c.8119-12A= (n.8119-12A=)
c.955-12A= (n.955-12A=)
c.8496-12A= (n.8496-12A=)
c.1053-12A=
c.8392-12A= (n.8392-12A=)
13g.32370944A>CCA2580087389BRCA2c.8488-12A>C (n.8488-12A>C)
c.8119-12A>C (n.8119-12A>C)
c.955-12A>C (n.955-12A>C)
c.8496-12A>C (n.8496-12A>C)
c.1053-12A>C
c.8392-12A>C (n.8392-12A>C)
 ClinVar gnomAD v4
13g.32370944A>GCA915946898BRCA2c.8488-12A>G (n.8488-12A>G)
c.8119-12A>G (n.8119-12A>G)
c.955-12A>G (n.955-12A>G)
c.8496-12A>G (n.8496-12A>G)
c.1053-12A>G
c.8392-12A>G (n.8392-12A>G)
 ClinVar dbSNP gnomAD v4
13g.32370945C>GCA2727920336BRCA2c.8488-11C>G (n.8488-11C>G)
c.8119-11C>G (n.8119-11C>G)
c.955-11C>G (n.955-11C>G)
c.8496-11C>G (n.8496-11C>G)
c.1053-11C>G
c.8392-11C>G (n.8392-11C>G)
 dbSNP
13g.32370945C>TCA2573149212BRCA2c.8488-11C>T (n.8488-11C>T)
c.8119-11C>T (n.8119-11C>T)
c.955-11C>T (n.955-11C>T)
c.8496-11C>T (n.8496-11C>T)
c.1053-11C>T
c.8392-11C>T (n.8392-11C>T)
 ClinVar dbSNP
13g.32370945_32370947dupCA2622601308BRCA2c.8488-11_8488-9dup (n.8488-11_8488-9dup)
c.8119-11_8119-9dup (n.8119-11_8119-9dup)
c.955-11_955-9dup (n.955-11_955-9dup)
c.8496-11_8496-9dup (n.8496-11_8496-9dup)
c.1053-11_1053-9dup
c.8392-11_8392-9dup (n.8392-11_8392-9dup)
 gnomAD v4
13g.32370946A=CA2082815191BRCA2c.8488-10A= (n.8488-10A=)
c.8119-10A= (n.8119-10A=)
c.955-10A= (n.955-10A=)
c.8496-10A= (n.8496-10A=)
c.1053-10A=
c.8392-10A= (n.8392-10A=)
13g.32370946A>CCA2727839512BRCA2c.8488-10A>C (n.8488-10A>C)
c.8119-10A>C (n.8119-10A>C)
c.955-10A>C (n.955-10A>C)
c.8496-10A>C (n.8496-10A>C)
c.1053-10A>C
c.8392-10A>C (n.8392-10A>C)
 dbSNP
13g.32370946A>GCA6941249BRCA2c.8488-10A>G (n.8488-10A>G)
c.8119-10A>G (n.8119-10A>G)
c.955-10A>G (n.955-10A>G)
c.8496-10A>G (n.8496-10A>G)
c.1053-10A>G
c.8392-10A>G (n.8392-10A>G)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32370946A>TCA2727839511BRCA2c.8488-10A>T (n.8488-10A>T)
c.8119-10A>T (n.8119-10A>T)
c.955-10A>T (n.955-10A>T)
c.8496-10A>T (n.8496-10A>T)
c.1053-10A>T
c.8392-10A>T (n.8392-10A>T)
 dbSNP
13g.32370947T>ACA2727920338BRCA2c.8488-9T>A (n.8488-9T>A)
c.8119-9T>A (n.8119-9T>A)
c.955-9T>A (n.955-9T>A)
c.8496-9T>A (n.8496-9T>A)
c.1053-9T>A
c.8392-9T>A (n.8392-9T>A)
 dbSNP
13g.32370947T>CCA2727920341BRCA2c.8488-9T>C (n.8488-9T>C)
c.8119-9T>C (n.8119-9T>C)
c.955-9T>C (n.955-9T>C)
c.8496-9T>C (n.8496-9T>C)
c.1053-9T>C
c.8392-9T>C (n.8392-9T>C)
 dbSNP
13g.32370947T>GCA2695217936BRCA2c.8488-9T>G (n.8488-9T>G)
c.8119-9T>G (n.8119-9T>G)
c.955-9T>G (n.955-9T>G)
c.8496-9T>G (n.8496-9T>G)
c.1053-9T>G
c.8392-9T>G (n.8392-9T>G)
 ClinVar
13g.32370948dupCA247483978BRCA2c.8488-8dup (n.8488-8dup)
c.8119-8dup (n.8119-8dup)
c.955-8dup (n.955-8dup)
c.8496-8dup (n.8496-8dup)
c.1053-8dup
c.8392-8dup (n.8392-8dup)
 dbSNP
13g.32370948T>ACA2622601309BRCA2c.8488-8T>A (n.8488-8T>A)
c.8119-8T>A (n.8119-8T>A)
c.955-8T>A (n.955-8T>A)
c.8496-8T>A (n.8496-8T>A)
c.1053-8T>A
c.8392-8T>A (n.8392-8T>A)
 gnomAD v4
13g.32370948T>CCA2573149213BRCA2c.8488-8T>C (n.8488-8T>C)
c.8119-8T>C (n.8119-8T>C)
c.955-8T>C (n.955-8T>C)
c.8496-8T>C (n.8496-8T>C)
c.1053-8T>C
c.8392-8T>C (n.8392-8T>C)
 ClinVar dbSNP
13g.32370948T>GCA025678BRCA2c.8488-8T>G (n.8488-8T>G)
c.8119-8T>G (n.8119-8T>G)
c.955-8T>G (n.955-8T>G)
c.8496-8T>G (n.8496-8T>G)
c.1053-8T>G
c.8392-8T>G (n.8392-8T>G)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32370948T=CA2082815201BRCA2c.8488-8T= (n.8488-8T=)
c.8119-8T= (n.8119-8T=)
c.955-8T= (n.955-8T=)
c.8496-8T= (n.8496-8T=)
c.1053-8T=
c.8392-8T= (n.8392-8T=)
13g.32370949A=CA2082815207BRCA2c.8488-7A= (n.8488-7A=)
c.8119-7A= (n.8119-7A=)
c.955-7A= (n.955-7A=)
c.8496-7A= (n.8496-7A=)
c.1053-7A=
c.8392-7A= (n.8392-7A=)
13g.32370949A>GCA658798060BRCA2c.8488-7A>G (n.8488-7A>G)
c.8119-7A>G (n.8119-7A>G)
c.955-7A>G (n.955-7A>G)
c.8496-7A>G (n.8496-7A>G)
c.1053-7A>G
c.8392-7A>G (n.8392-7A>G)
 ClinVar dbSNP
13g.32370950T>ACA2727920376BRCA2c.8488-6T>A (n.8488-6T>A)
c.8119-6T>A (n.8119-6T>A)
c.955-6T>A (n.955-6T>A)
c.8496-6T>A (n.8496-6T>A)
c.1053-6T>A
c.8392-6T>A (n.8392-6T>A)
 dbSNP
13g.32370950T>GCA2727920343BRCA2c.8488-6T>G (n.8488-6T>G)
c.8119-6T>G (n.8119-6T>G)
c.955-6T>G (n.955-6T>G)
c.8496-6T>G (n.8496-6T>G)
c.1053-6T>G
c.8392-6T>G (n.8392-6T>G)
 dbSNP
13g.32370951T>CCA6941250BRCA2c.8488-5T>C (n.8488-5T>C)
c.8119-5T>C (n.8119-5T>C)
c.955-5T>C (n.955-5T>C)
c.8496-5T>C (n.8496-5T>C)
c.1053-5T>C
c.8392-5T>C (n.8392-5T>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32370951T>GCA2580087390BRCA2c.8488-5T>G (n.8488-5T>G)
c.8119-5T>G (n.8119-5T>G)
c.955-5T>G (n.955-5T>G)
c.8496-5T>G (n.8496-5T>G)
c.1053-5T>G
c.8392-5T>G (n.8392-5T>G)
 ClinVar
13g.32370951T=CA2082815216BRCA2c.8488-5T= (n.8488-5T=)
c.8119-5T= (n.8119-5T=)
c.955-5T= (n.955-5T=)
c.8496-5T= (n.8496-5T=)
c.1053-5T=
c.8392-5T= (n.8392-5T=)
13g.32370952A>GCA1139768296BRCA2c.8488-4A>G (n.8488-4A>G)
c.8119-4A>G (n.8119-4A>G)
c.955-4A>G (n.955-4A>G)
c.8496-4A>G (n.8496-4A>G)
c.1053-4A>G
c.8392-4A>G (n.8392-4A>G)
 dbSNP
13g.32370952A>TCA2727920387BRCA2c.8488-4A>T (n.8488-4A>T)
c.8119-4A>T (n.8119-4A>T)
c.955-4A>T (n.955-4A>T)
c.8496-4A>T (n.8496-4A>T)
c.1053-4A>T
c.8392-4A>T (n.8392-4A>T)
 dbSNP
13g.32370953C>ACA2082815218BRCA2c.8488-3C>A (n.8488-3C>A)
c.8119-3C>A (n.8119-3C>A)
c.955-3C>A (n.955-3C>A)
c.8496-3C>A (n.8496-3C>A)
c.1053-3C>A
c.8392-3C>A (n.8392-3C>A)
 ClinVar dbSNP
13g.32370953C=CA2082815222BRCA2c.8488-3C= (n.8488-3C=)
c.8119-3C= (n.8119-3C=)
c.955-3C= (n.955-3C=)
c.8496-3C= (n.8496-3C=)
c.1053-3C=
c.8392-3C= (n.8392-3C=)
13g.32370953C>GCA916080521BRCA2c.8488-3C>G (n.8488-3C>G)
c.8119-3C>G (n.8119-3C>G)
c.955-3C>G (n.955-3C>G)
c.8496-3C>G (n.8496-3C>G)
c.1053-3C>G
c.8392-3C>G (n.8392-3C>G)
 ClinVar dbSNP
13g.32370953C>TCA913188610BRCA2c.8488-3C>T (n.8488-3C>T)
c.8119-3C>T (n.8119-3C>T)
c.955-3C>T (n.955-3C>T)
c.8496-3C>T (n.8496-3C>T)
c.1053-3C>T
c.8392-3C>T (n.8392-3C>T)
 ClinVar dbSNP
13g.32370954A=CA2082815228BRCA2c.8488-2A= (n.8488-2A=)
c.8119-2A= (n.8119-2A=)
c.955-2A= (n.955-2A=)
c.8496-2A= (n.8496-2A=)
c.1053-2A=
c.8392-2A= (n.8392-2A=)
13g.32370954A>CCA387752652BRCA2c.8488-2A>C (n.8488-2A>C)
c.8119-2A>C (n.8119-2A>C)
c.955-2A>C (n.955-2A>C)
c.8496-2A>C (n.8496-2A>C)
c.1053-2A>C
c.8392-2A>C (n.8392-2A>C)
 ClinVar dbSNP
13g.32370954A>GCA6941251BRCA2c.8488-2A>G (n.8488-2A>G)
c.8119-2A>G (n.8119-2A>G)
c.955-2A>G (n.955-2A>G)
c.8496-2A>G (n.8496-2A>G)
c.1053-2A>G
c.8392-2A>G (n.8392-2A>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.32370954A>TCA387752653BRCA2c.8488-2A>T (n.8488-2A>T)
c.8119-2A>T (n.8119-2A>T)
c.955-2A>T (n.955-2A>T)
c.8496-2A>T (n.8496-2A>T)
c.1053-2A>T
c.8392-2A>T (n.8392-2A>T)
 dbSNP
13g.32370954_32370957delinsAGTGCA2082815232BRCA2c.8488-2_8489delinsAGTG
c.8119-2_8120delinsAGTG
c.955-2_956delinsAGTG
c.8496-2_8497delinsAGTG
c.1053-2_1054delinsAGTG
c.8392-2_8393delinsAGTG
13g.32370954_32370964delinsAGTGGATGGAGCA2082815234BRCA2c.8488-2_8496delinsAGTGGATGGAG
c.8119-2_8127delinsAGTGGATGGAG
c.955-2_963delinsAGTGGATGGAG
c.8496-2_8504delinsAGTGGATGGAG
c.1053-2_1061delinsAGTGGATGGAG
c.8392-2_8400delinsAGTGGATGGAG
13g.32370955G>ACA025677BRCA2c.8488-1G>A (n.8488-1G>A)
c.8119-1G>A (n.8119-1G>A)
c.955-1G>A (n.955-1G>A)
c.8496-1G>A (n.8496-1G>A)
c.1053-1G>A
c.8392-1G>A (n.8392-1G>A)
 ClinVar dbSNP gnomAD v4
13g.32370955G>CCA387752654BRCA2c.8488-1G>C (n.8488-1G>C)
c.8119-1G>C (n.8119-1G>C)
c.955-1G>C (n.955-1G>C)
c.8496-1G>C (n.8496-1G>C)
c.1053-1G>C
c.8392-1G>C (n.8392-1G>C)
 ClinVar dbSNP
13g.32370955G=CA2082815246BRCA2c.8488-1G= (n.8488-1G=)
c.8119-1G= (n.8119-1G=)
c.955-1G= (n.955-1G=)
c.8496-1G= (n.8496-1G=)
c.1053-1G=
c.8392-1G= (n.8392-1G=)
13g.32370955G>TCA10602549BRCA2c.8488-1G>T (n.8488-1G>T)
c.8119-1G>T (n.8119-1G>T)
c.955-1G>T (n.955-1G>T)
c.8496-1G>T (n.8496-1G>T)
c.1053-1G>T
c.8392-1G>T (n.8392-1G>T)
 ClinVar dbSNP
13g.32370955_32370957delinsTCCATTACACA913190914BRCA2c.8488-1_8489delinsTCCATTACA
c.8119-1_8120delinsTCCATTACA
c.955-1_956delinsTCCATTACA
c.8496-1_8497delinsTCCATTACA
c.1053-1_1054delinsTCCATTACA
c.8392-1_8393delinsTCCATTACA
 ClinVar dbSNP
13g.32370956_32370957delCA10586590BRCA2c.8488_8489del
c.8119_8120del
c.955_956del
c.8496_8497del
c.1053_1054del
c.8392_8393del
 ClinVar dbSNP
13g.32370955_32370964delinsCTCA658656379BRCA2c.8488-1_8496delinsCT
c.8119-1_8127delinsCT
c.955-1_963delinsCT
c.8496-1_8504delinsCT
c.1053-1_1061delinsCT
c.8392-1_8400delinsCT
 ClinVar dbSNP
13g.32370956T>ACA387752655BRCA2c.8488T>A (p.Trp2830Arg)
c.8119T>A (p.Trp2707Arg)
c.955T>A (p.Trp319Arg)
c.8496T>A (n.8496T>A)
c.1053T>A
c.8392T>A (p.Trp2798Arg)
 ClinVar dbSNP
13g.32370956T>CCA387752656BRCA2c.8488T>C (p.Trp2830Arg)
c.8119T>C (p.Trp2707Arg)
c.955T>C (p.Trp319Arg)
c.8496T>C (n.8496T>C)
c.1053T>C
c.8392T>C (p.Trp2798Arg)
 ClinVar dbSNP
13g.32370956T>GCA387752657BRCA2c.8488T>G (p.Trp2830Gly)
c.8119T>G (p.Trp2707Gly)
c.955T>G (p.Trp319Gly)
c.8496T>G (n.8496T>G)
c.1053T>G
c.8392T>G (p.Trp2798Gly)
 gnomAD v4
13g.32370956T=CA2082815262BRCA2c.8488T= (p.Trp2830=)
c.8119T= (p.Trp2707=)
c.955T= (p.Trp319=)
c.8496T= (n.8496T=)
c.1053T=
c.8392T= (p.Trp2798=)
13g.32370957G>ACA025679BRCA2c.8489G>A (p.Trp2830Ter)
c.8120G>A (p.Trp2707Ter)
c.956G>A (p.Trp319Ter)
c.8497G>A (n.8497G>A)
c.1054G>A
c.8393G>A (p.Trp2798Ter)
 ClinVar dbSNP
13g.32370957G>CCA387752658BRCA2c.8489G>C (p.Trp2830Ser)
c.8120G>C (p.Trp2707Ser)
c.956G>C (p.Trp319Ser)
c.8497G>C (n.8497G>C)
c.1054G>C
c.8393G>C (p.Trp2798Ser)
 ClinVar dbSNP
13g.32370957G=CA2082815276BRCA2c.8489G= (p.Trp2830=)
c.8120G= (p.Trp2707=)
c.956G= (p.Trp319=)
c.8497G= (n.8497G=)
c.1054G=
c.8393G= (p.Trp2798=)
13g.32370957G>TCA387752659BRCA2c.8489G>T (p.Trp2830Leu)
c.8120G>T (p.Trp2707Leu)
c.956G>T (p.Trp319Leu)
c.8497G>T (n.8497G>T)
c.1054G>T
c.8393G>T (p.Trp2798Leu)
 dbSNP
13g.32370958G>ACA025681BRCA2c.8490G>A (p.Trp2830Ter)
c.8121G>A (p.Trp2707Ter)
c.957G>A (p.Trp319Ter)
c.8498G>A (n.8498G>A)
c.1055G>A
c.8394G>A (p.Trp2798Ter)
 ClinVar dbSNP
13g.32370958G>CCA387752660BRCA2c.8490G>C (p.Trp2830Cys)
c.8121G>C (p.Trp2707Cys)
c.957G>C (p.Trp319Cys)
c.8498G>C (n.8498G>C)
c.1055G>C
c.8394G>C (p.Trp2798Cys)
 dbSNP
13g.32370958G=CA2082815282BRCA2c.8490G= (p.Trp2830=)
c.8121G= (p.Trp2707=)
c.957G= (p.Trp319=)
c.8498G= (n.8498G=)
c.1055G=
c.8394G= (p.Trp2798=)
13g.32370958G>TCA387752661BRCA2c.8490G>T (p.Trp2830Cys)
c.8121G>T (p.Trp2707Cys)
c.957G>T (p.Trp319Cys)
c.8498G>T (n.8498G>T)
c.1055G>T
c.8394G>T (p.Trp2798Cys)
 dbSNP
13g.32370959A=CA2082815293BRCA2c.8491A= (p.Met2831=)
c.8122A= (p.Met2708=)
c.958A= (p.Met320=)
c.8499A= (n.8499A=)
c.1056A=
c.8395A= (p.Met2799=)
13g.32370959A>CCA387752662BRCA2c.8491A>C (p.Met2831Leu)
c.8122A>C (p.Met2708Leu)
c.958A>C (p.Met320Leu)
c.8499A>C (n.8499A>C)
c.1056A>C
c.8395A>C (p.Met2799Leu)
13g.32370959A>GCA6941252BRCA2c.8491A>G (p.Met2831Val)
c.8122A>G (p.Met2708Val)
c.958A>G (p.Met320Val)
c.8499A>G (n.8499A>G)
c.1056A>G
c.8395A>G (p.Met2799Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32370959A>TCA387752663BRCA2c.8491A>T (p.Met2831Leu)
c.8122A>T (p.Met2708Leu)
c.958A>T (p.Met320Leu)
c.8499A>T (n.8499A>T)
c.1056A>T
c.8395A>T (p.Met2799Leu)
 ClinVar dbSNP
13g.32370960T>ACA387752664BRCA2c.8492T>A (p.Met2831Lys)
c.8123T>A (p.Met2708Lys)
c.959T>A (p.Met320Lys)
c.8500T>A (n.8500T>A)
c.1057T>A
c.8396T>A (p.Met2799Lys)
13g.32370960T>CCA387752665BRCA2c.8492T>C (p.Met2831Thr)
c.8123T>C (p.Met2708Thr)
c.959T>C (p.Met320Thr)
c.8500T>C (n.8500T>C)
c.1057T>C
c.8396T>C (p.Met2799Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32370960T>GCA387752666BRCA2c.8492T>G (p.Met2831Arg)
c.8123T>G (p.Met2708Arg)
c.959T>G (p.Met320Arg)
c.8500T>G (n.8500T>G)
c.1057T>G
c.8396T>G (p.Met2799Arg)
 ClinVar dbSNP
13g.32370960T=CA2082815298BRCA2c.8492T= (p.Met2831=)
c.8123T= (p.Met2708=)
c.959T= (p.Met320=)
c.8500T= (n.8500T=)
c.1057T=
c.8396T= (p.Met2799=)
13g.32370961G>ACA387752667BRCA2c.8493G>A (p.Met2831Ile)
c.8124G>A (p.Met2708Ile)
c.960G>A (p.Met320Ile)
c.8501G>A (n.8501G>A)
c.1058G>A
c.8397G>A (p.Met2799Ile)
 ClinVar dbSNP gnomAD v4
13g.32370961G>CCA387752668BRCA2c.8493G>C (p.Met2831Ile)
c.8124G>C (p.Met2708Ile)
c.960G>C (p.Met320Ile)
c.8501G>C (n.8501G>C)
c.1058G>C
c.8397G>C (p.Met2799Ile)
 dbSNP
13g.32370961G>TCA387752669BRCA2c.8493G>T (p.Met2831Ile)
c.8124G>T (p.Met2708Ile)
c.960G>T (p.Met320Ile)
c.8501G>T (n.8501G>T)
c.1058G>T
c.8397G>T (p.Met2799Ile)
 dbSNP
13g.32370962G>ACA387752670BRCA2c.8494G>A (p.Glu2832Lys)
c.8125G>A (p.Glu2709Lys)
c.961G>A (p.Glu321Lys)
c.8502G>A (n.8502G>A)
c.1059G>A
c.8398G>A (p.Glu2800Lys)
 ClinVar dbSNP
13g.32370962G>CCA10579790BRCA2c.8494G>C (p.Glu2832Gln)
c.8125G>C (p.Glu2709Gln)
c.961G>C (p.Glu321Gln)
c.8502G>C (n.8502G>C)
c.1059G>C
c.8398G>C (p.Glu2800Gln)
 ClinVar dbSNP
13g.32370962G=CA2082815310BRCA2c.8494G= (p.Glu2832=)
c.8125G= (p.Glu2709=)
c.961G= (p.Glu321=)
c.8502G= (n.8502G=)
c.1059G=
c.8398G= (p.Glu2800=)
13g.32370962G>TCA387752671BRCA2c.8494G>T (p.Glu2832Ter)
c.8125G>T (p.Glu2709Ter)
c.961G>T (p.Glu321Ter)
c.8502G>T (n.8502G>T)
c.1059G>T
c.8398G>T (p.Glu2800Ter)
 ClinVar dbSNP
13g.32370963A=CA2082815323BRCA2c.8495A= (p.Glu2832=)
c.8126A= (p.Glu2709=)
c.962A= (p.Glu321=)
c.8503A= (n.8503A=)
c.1060A=
c.8399A= (p.Glu2800=)
13g.32370963A>CCA387752672BRCA2c.8495A>C (p.Glu2832Ala)
c.8126A>C (p.Glu2709Ala)
c.962A>C (p.Glu321Ala)
c.8503A>C (n.8503A>C)
c.1060A>C
c.8399A>C (p.Glu2800Ala)
13g.32370963A>GCA6941253BRCA2c.8495A>G (p.Glu2832Gly)
c.8126A>G (p.Glu2709Gly)
c.962A>G (p.Glu321Gly)
c.8503A>G (n.8503A>G)
c.1060A>G
c.8399A>G (p.Glu2800Gly)
 dbSNP ExAC gnomAD v2
13g.32370963A>TCA387752673BRCA2c.8495A>T (p.Glu2832Val)
c.8126A>T (p.Glu2709Val)
c.962A>T (p.Glu321Val)
c.8503A>T (n.8503A>T)
c.1060A>T
c.8399A>T (p.Glu2800Val)
 dbSNP
13g.32370964G>ACA483261493BRCA2c.8496G>A (p.Glu2832=)
c.8127G>A (p.Glu2709=)
c.963G>A (p.Glu321=)
c.8504G>A (n.8504G>A)
c.1061G>A
c.8400G>A (p.Glu2800=)
 dbSNP
13g.32370964G>CCA387752674BRCA2c.8496G>C (p.Glu2832Asp)
c.8127G>C (p.Glu2709Asp)
c.963G>C (p.Glu321Asp)
c.8504G>C (n.8504G>C)
c.1061G>C
c.8400G>C (p.Glu2800Asp)
 dbSNP
13g.32370964G>TCA387752675BRCA2c.8496G>T (p.Glu2832Asp)
c.8127G>T (p.Glu2709Asp)
c.963G>T (p.Glu321Asp)
c.8504G>T (n.8504G>T)
c.1061G>T
c.8400G>T (p.Glu2800Asp)
 dbSNP
13g.32370965A=CA2082815338BRCA2c.8497A= (p.Lys2833=)
c.8128A= (p.Lys2710=)
c.964A= (p.Lys322=)
c.8505A= (n.8505A=)
c.1062A=
c.8401A= (p.Lys2801=)
13g.32370965A>CCA387752676BRCA2c.8497A>C (p.Lys2833Gln)
c.8128A>C (p.Lys2710Gln)
c.964A>C (p.Lys322Gln)
c.8505A>C (n.8505A>C)
c.1062A>C
c.8401A>C (p.Lys2801Gln)
 dbSNP
13g.32370965A>GCA387752677BRCA2c.8497A>G (p.Lys2833Glu)
c.8128A>G (p.Lys2710Glu)
c.964A>G (p.Lys322Glu)
c.8505A>G (n.8505A>G)
c.1062A>G
c.8401A>G (p.Lys2801Glu)
 dbSNP gnomAD v3 gnomAD v4
13g.32370965A>TCA387752678BRCA2c.8497A>T (p.Lys2833Ter)
c.8128A>T (p.Lys2710Ter)
c.964A>T (p.Lys322Ter)
c.8505A>T (n.8505A>T)
c.1062A>T
c.8401A>T (p.Lys2801Ter)
 ClinVar dbSNP
13g.32370966A>CCA387752679BRCA2c.8498A>C (p.Lys2833Thr)
c.8129A>C (p.Lys2710Thr)
c.965A>C (p.Lys322Thr)
c.8506A>C (n.8506A>C)
c.1063A>C
c.8402A>C (p.Lys2801Thr)
 ClinVar
13g.32370966A>GCA387752680BRCA2c.8498A>G (p.Lys2833Arg)
c.8129A>G (p.Lys2710Arg)
c.965A>G (p.Lys322Arg)
c.8506A>G (n.8506A>G)
c.1063A>G
c.8402A>G (p.Lys2801Arg)
 COSMIC COSMIC
13g.32370966A>TCA387752681BRCA2c.8498A>T (p.Lys2833Met)
c.8129A>T (p.Lys2710Met)
c.965A>T (p.Lys322Met)
c.8506A>T (n.8506A>T)
c.1063A>T
c.8402A>T (p.Lys2801Met)
 dbSNP
13g.32370967G>ACA025682BRCA2c.8499G>A (p.Lys2833=)
c.8130G>A (p.Lys2710=)
c.966G>A (p.Lys322=)
c.8507G>A (n.8507G>A)
c.1064G>A
c.8403G>A (p.Lys2801=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32370967G>CCA10579791BRCA2c.8499G>C (p.Lys2833Asn)
c.8130G>C (p.Lys2710Asn)
c.966G>C (p.Lys322Asn)
c.8507G>C (n.8507G>C)
c.1064G>C
c.8403G>C (p.Lys2801Asn)
 ClinVar dbSNP
13g.32370967G=CA2082815350BRCA2c.8499G= (p.Lys2833=)
c.8130G= (p.Lys2710=)
c.966G= (p.Lys322=)
c.8507G= (n.8507G=)
c.1064G=
c.8403G= (p.Lys2801=)
13g.32370967G>TCA387752682BRCA2c.8499G>T (p.Lys2833Asn)
c.8130G>T (p.Lys2710Asn)
c.966G>T (p.Lys322Asn)
c.8507G>T (n.8507G>T)
c.1064G>T
c.8403G>T (p.Lys2801Asn)
 dbSNP
13g.32370968A=CA2082815362BRCA2c.8500A= (p.Thr2834=)
c.8131A= (p.Thr2711=)
c.967A= (p.Thr323=)
c.8508A= (n.8508A=)
c.1065A=
c.8404A= (p.Thr2802=)
13g.32370968A>CCA387752683BRCA2c.8500A>C (p.Thr2834Pro)
c.8131A>C (p.Thr2711Pro)
c.967A>C (p.Thr323Pro)
c.8508A>C (n.8508A>C)
c.1065A>C
c.8404A>C (p.Thr2802Pro)
13g.32370968A>GCA10575931BRCA2c.8500A>G (p.Thr2834Ala)
c.8131A>G (p.Thr2711Ala)
c.967A>G (p.Thr323Ala)
c.8508A>G (n.8508A>G)
c.1065A>G
c.8404A>G (p.Thr2802Ala)
 ClinVar dbSNP
13g.32370968A>TCA387752684BRCA2c.8500A>T (p.Thr2834Ser)
c.8131A>T (p.Thr2711Ser)
c.967A>T (p.Thr323Ser)
c.8508A>T (n.8508A>T)
c.1065A>T
c.8404A>T (p.Thr2802Ser)
 dbSNP
13g.32370968_32370969delinsACCA2082815359BRCA2c.8500_8501delinsAC (p.Thr2834=)
c.8131_8132delinsAC (p.Thr2711=)
c.967_968delinsAC (p.Thr323=)
c.8508_8509delinsAC (n.8508_8509delinsAC)
c.1065_1066delinsAC
c.8404_8405delinsAC (p.Thr2802=)
13g.32370969delCA025683BRCA2c.8501del (p.Thr2834AsnfsTer29)
c.8132del (p.Thr2711AsnfsTer29)
c.968del (p.Thr323AsnfsTer29)
c.8509del (n.8509del)
c.1066del
c.8405del (p.Thr2802AsnfsTer29)
 ClinVar dbSNP
13g.32370969C>ACA387752685BRCA2c.8501C>A (p.Thr2834Lys)
c.8132C>A (p.Thr2711Lys)
c.968C>A (p.Thr323Lys)
c.8509C>A (n.8509C>A)
c.1066C>A
c.8405C>A (p.Thr2802Lys)
 dbSNP
13g.32370969C=CA2082815379BRCA2c.8501C= (p.Thr2834=)
c.8132C= (p.Thr2711=)
c.968C= (p.Thr323=)
c.8509C= (n.8509C=)
c.1066C=
c.8405C= (p.Thr2802=)
13g.32370969C>GCA387752686BRCA2c.8501C>G (p.Thr2834Arg)
c.8132C>G (p.Thr2711Arg)
c.968C>G (p.Thr323Arg)
c.8509C>G (n.8509C>G)
c.1066C>G
c.8405C>G (p.Thr2802Arg)
 ClinVar dbSNP
13g.32370969C>TCA387752687BRCA2c.8501C>T (p.Thr2834Ile)
c.8132C>T (p.Thr2711Ile)
c.968C>T (p.Thr323Ile)
c.8509C>T (n.8509C>T)
c.1066C>T
c.8405C>T (p.Thr2802Ile)
 dbSNP
13g.32370973_32370975delCA2739277519BRCA2c.8505_8507del (p.Ser2836del)
c.8136_8138del (p.Ser2713del)
c.972_974del (p.Ser325del)
c.8513_8515del (n.8513_8515del)
c.1070_1072del
c.8409_8411del (p.Ser2804del)
 ClinVar
13g.32370970A=CA2082815388BRCA2c.8502A= (p.Thr2834=)
c.8133A= (p.Thr2711=)
c.969A= (p.Thr323=)
c.8510A= (n.8510A=)
c.1067A=
c.8406A= (p.Thr2802=)
13g.32370970A>CCA483261494BRCA2c.8502A>C (p.Thr2834=)
c.8133A>C (p.Thr2711=)
c.969A>C (p.Thr323=)
c.8510A>C (n.8510A>C)
c.1067A>C
c.8406A>C (p.Thr2802=)
13g.32370970A>GCA483261495BRCA2c.8502A>G (p.Thr2834=)
c.8133A>G (p.Thr2711=)
c.969A>G (p.Thr323=)
c.8510A>G (n.8510A>G)
c.1067A>G
c.8406A>G (p.Thr2802=)
 ClinVar dbSNP
13g.32370970A>TCA483261496BRCA2c.8502A>T (p.Thr2834=)
c.8133A>T (p.Thr2711=)
c.969A>T (p.Thr323=)
c.8510A>T (n.8510A>T)
c.1067A>T
c.8406A>T (p.Thr2802=)
 dbSNP
13g.32370971T>ACA387752688BRCA2c.8503T>A (p.Ser2835Thr)
c.8134T>A (p.Ser2712Thr)
c.970T>A (p.Ser324Thr)
c.8511T>A (n.8511T>A)
c.1068T>A
c.1T>A (p.Ser1Thr)
c.8407T>A (p.Ser2803Thr)
 dbSNP
13g.32370971T>CCA025684BRCA2c.8503T>C (p.Ser2835Pro)
c.8134T>C (p.Ser2712Pro)
c.970T>C (p.Ser324Pro)
c.8511T>C (n.8511T>C)
c.1068T>C
c.1T>C (p.Ser1Pro)
c.8407T>C (p.Ser2803Pro)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32370971T>GCA387752689BRCA2c.8503T>G (p.Ser2835Ala)
c.8134T>G (p.Ser2712Ala)
c.970T>G (p.Ser324Ala)
c.8511T>G (n.8511T>G)
c.1068T>G
c.1T>G (p.Ser1Ala)
c.8407T>G (p.Ser2803Ala)
13g.32370971T=CA2082815394BRCA2c.8503T= (p.Ser2835=)
c.8134T= (p.Ser2712=)
c.970T= (p.Ser324=)
c.8511T= (n.8511T=)
c.1068T=
c.1T= (p.Ser1=)
c.8407T= (p.Ser2803=)
13g.32370972C>ACA025685BRCA2c.8504C>A (p.Ser2835Ter)
c.8135C>A (p.Ser2712Ter)
c.971C>A (p.Ser324Ter)
c.8512C>A (n.8512C>A)
c.1069C>A
c.2C>A (p.Ser1Ter)
c.8408C>A (p.Ser2803Ter)
 ClinVar dbSNP COSMIC COSMIC
13g.32370972C=CA2082815405BRCA2c.8504C= (p.Ser2835=)
c.8135C= (p.Ser2712=)
c.971C= (p.Ser324=)
c.8512C= (n.8512C=)
c.1069C=
c.2C= (p.Ser1=)
c.8408C= (p.Ser2803=)
13g.32370972C>GCA10589501BRCA2c.8504C>G (p.Ser2835Ter)
c.8135C>G (p.Ser2712Ter)
c.971C>G (p.Ser324Ter)
c.8512C>G (n.8512C>G)
c.1069C>G
c.2C>G (p.Ser1Ter)
c.8408C>G (p.Ser2803Ter)
 ClinVar dbSNP
13g.32370972C>TCA387752690BRCA2c.8504C>T (p.Ser2835Leu)
c.8135C>T (p.Ser2712Leu)
c.971C>T (p.Ser324Leu)
c.8512C>T (n.8512C>T)
c.1069C>T
c.2C>T (p.Ser1Leu)
c.8408C>T (p.Ser2803Leu)
 dbSNP
13g.32370972_32370973delinsCACA2082815406BRCA2c.8504_8505delinsCA (p.Ser2835=)
c.8135_8136delinsCA (p.Ser2712=)
c.971_972delinsCA (p.Ser324=)
c.8512_8513delinsCA (n.8512_8513delinsCA)
c.1069_1070delinsCA
c.2_3delinsCA (p.Ser1=)
c.8408_8409delinsCA (p.Ser2803=)
13g.32370973delCA025686BRCA2c.8505del (p.Ser2836LeufsTer27)
c.8136del (p.Ser2713LeufsTer27)
c.972del (p.Ser325LeufsTer27)
c.8513del (n.8513del)
c.1070del
c.3del (p.Ser2LeufsTer27)
c.8409del (p.Ser2804LeufsTer27)
 ClinVar dbSNP
13g.32370973A=CA2082815421BRCA2c.8505A= (p.Ser2835=)
c.8136A= (p.Ser2712=)
c.972A= (p.Ser324=)
c.8513A= (n.8513A=)
c.1070A=
c.3A= (p.Ser1=)
c.8409A= (p.Ser2803=)
13g.32370973A>CCA483261497BRCA2c.8505A>C (p.Ser2835=)
c.8136A>C (p.Ser2712=)
c.972A>C (p.Ser324=)
c.8513A>C (n.8513A>C)
c.1070A>C
c.3A>C (p.Ser1=)
c.8409A>C (p.Ser2803=)
13g.32370973A>GCA6941254BRCA2c.8505A>G (p.Ser2835=)
c.8136A>G (p.Ser2712=)
c.972A>G (p.Ser324=)
c.8513A>G (n.8513A>G)
c.1070A>G
c.3A>G (p.Ser1=)
c.8409A>G (p.Ser2803=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32370973A>TCA483261498BRCA2c.8505A>T (p.Ser2835=)
c.8136A>T (p.Ser2712=)
c.972A>T (p.Ser324=)
c.8513A>T (n.8513A>T)
c.1070A>T
c.3A>T (p.Ser1=)
c.8409A>T (p.Ser2803=)
 dbSNP
13g.32370974T>ACA387752691BRCA2c.8506T>A (p.Ser2836Thr)
c.8137T>A (p.Ser2713Thr)
c.973T>A (p.Ser325Thr)
c.8514T>A (n.8514T>A)
c.1071T>A
c.4T>A (p.Ser2Thr)
c.8410T>A (p.Ser2804Thr)
 dbSNP
13g.32370974T>CCA387752692BRCA2c.8506T>C (p.Ser2836Pro)
c.8137T>C (p.Ser2713Pro)
c.973T>C (p.Ser325Pro)
c.8514T>C (n.8514T>C)
c.1071T>C
c.4T>C (p.Ser2Pro)
c.8410T>C (p.Ser2804Pro)
 ClinVar dbSNP
13g.32370974T>GCA387752693BRCA2c.8506T>G (p.Ser2836Ala)
c.8137T>G (p.Ser2713Ala)
c.973T>G (p.Ser325Ala)
c.8514T>G (n.8514T>G)
c.1071T>G
c.4T>G (p.Ser2Ala)
c.8410T>G (p.Ser2804Ala)
13g.32370974T=CA2082815432BRCA2c.8506T= (p.Ser2836=)
c.8137T= (p.Ser2713=)
c.973T= (p.Ser325=)
c.8514T= (n.8514T=)
c.1071T=
c.4T= (p.Ser2=)
c.8410T= (p.Ser2804=)
13g.32370975_32370976dupCA2573149214BRCA2c.8507_8508dup (p.Gly2837LeufsTer27)
c.8138_8139dup (p.Gly2714LeufsTer27)
c.974_975dup (p.Gly326LeufsTer27)
c.8515_8516dup (n.8515_8516dup)
c.1072_1073dup
c.5_6dup (p.Gly3LeufsTer27)
c.8411_8412dup (p.Gly2805LeufsTer27)
 ClinVar dbSNP
13g.32370975C>ACA387752694BRCA2c.8507C>A (p.Ser2836Tyr)
c.8138C>A (p.Ser2713Tyr)
c.974C>A (p.Ser325Tyr)
c.8515C>A (n.8515C>A)
c.1072C>A
c.5C>A (p.Ser2Tyr)
c.8411C>A (p.Ser2804Tyr)
13g.32370975C=CA2082815436BRCA2c.8507C= (p.Ser2836=)
c.8138C= (p.Ser2713=)
c.974C= (p.Ser325=)
c.8515C= (n.8515C=)
c.1072C=
c.5C= (p.Ser2=)
c.8411C= (p.Ser2804=)
13g.32370975C>GCA387752695BRCA2c.8507C>G (p.Ser2836Cys)
c.8138C>G (p.Ser2713Cys)
c.974C>G (p.Ser325Cys)
c.8515C>G (n.8515C>G)
c.1072C>G
c.5C>G (p.Ser2Cys)
c.8411C>G (p.Ser2804Cys)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32370975C>TCA336295BRCA2c.8507C>T (p.Ser2836Phe)
c.8138C>T (p.Ser2713Phe)
c.974C>T (p.Ser325Phe)
c.8515C>T (n.8515C>T)
c.1072C>T
c.5C>T (p.Ser2Phe)
c.8411C>T (p.Ser2804Phe)
 ClinVar dbSNP
13g.32370976T>ACA483261499BRCA2c.8508T>A (p.Ser2836=)
c.8139T>A (p.Ser2713=)
c.975T>A (p.Ser325=)
c.8516T>A (n.8516T>A)
c.1073T>A
c.6T>A (p.Ser2=)
c.8412T>A (p.Ser2804=)
13g.32370976T>CCA336270BRCA2c.8508T>C (p.Ser2836=)
c.8139T>C (p.Ser2713=)
c.975T>C (p.Ser325=)
c.8516T>C (n.8516T>C)
c.1073T>C
c.6T>C (p.Ser2=)
c.8412T>C (p.Ser2804=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32370976T>GCA483261500BRCA2c.8508T>G (p.Ser2836=)
c.8139T>G (p.Ser2713=)
c.975T>G (p.Ser325=)
c.8516T>G (n.8516T>G)
c.1073T>G
c.6T>G (p.Ser2=)
c.8412T>G (p.Ser2804=)
13g.32370976T=CA2082815449BRCA2c.8508T= (p.Ser2836=)
c.8139T= (p.Ser2713=)
c.975T= (p.Ser325=)
c.8516T= (n.8516T=)
c.1073T=
c.6T= (p.Ser2=)
c.8412T= (p.Ser2804=)
13g.32370977G>ACA387752698BRCA2c.8509G>A (p.Gly2837Arg)
c.8140G>A (p.Gly2714Arg)
c.976G>A (p.Gly326Arg)
c.8517G>A (n.8517G>A)
c.1074G>A
c.7G>A (p.Gly3Arg)
c.8413G>A (p.Gly2805Arg)
 dbSNP
13g.32370977G>CCA387752696BRCA2c.8509G>C (p.Gly2837Arg)
c.8140G>C (p.Gly2714Arg)
c.976G>C (p.Gly326Arg)
c.8517G>C (n.8517G>C)
c.1074G>C
c.7G>C (p.Gly3Arg)
c.8413G>C (p.Gly2805Arg)
 dbSNP
13g.32370977G>TCA387752697BRCA2c.8509G>T (p.Gly2837Ter)
c.8140G>T (p.Gly2714Ter)
c.976G>T (p.Gly326Ter)
c.8517G>T (n.8517G>T)
c.1074G>T
c.7G>T (p.Gly3Ter)
c.8413G>T (p.Gly2805Ter)
 dbSNP COSMIC COSMIC
13g.32370978G>ACA387752699BRCA2c.8510G>A (p.Gly2837Glu)
c.8141G>A (p.Gly2714Glu)
c.977G>A (p.Gly326Glu)
c.8518G>A (n.8518G>A)
c.1075G>A
c.8G>A (p.Gly3Glu)
c.8414G>A (p.Gly2805Glu)
 dbSNP gnomAD v4
13g.32370978G>CCA387752700BRCA2c.8510G>C (p.Gly2837Ala)
c.8141G>C (p.Gly2714Ala)
c.977G>C (p.Gly326Ala)
c.8518G>C (n.8518G>C)
c.1075G>C
c.8G>C (p.Gly3Ala)
c.8414G>C (p.Gly2805Ala)
 dbSNP gnomAD v4
13g.32370978G=CA2082815460BRCA2c.8510G= (p.Gly2837=)
c.8141G= (p.Gly2714=)
c.977G= (p.Gly326=)
c.8518G= (n.8518G=)
c.1075G=
c.8G= (p.Gly3=)
c.8414G= (p.Gly2805=)
13g.32370978G>TCA025687BRCA2c.8510G>T (p.Gly2837Val)
c.8141G>T (p.Gly2714Val)
c.977G>T (p.Gly326Val)
c.8518G>T (n.8518G>T)
c.1075G>T
c.8G>T (p.Gly3Val)
c.8414G>T (p.Gly2805Val)
 ClinVar dbSNP COSMIC COSMIC
13g.32370979A>CCA483261501BRCA2c.8511A>C (p.Gly2837=)
c.8142A>C (p.Gly2714=)
c.978A>C (p.Gly326=)
c.8519A>C (n.8519A>C)
c.1076A>C
c.9A>C (p.Gly3=)
c.8415A>C (p.Gly2805=)
13g.32370979A>GCA483261502BRCA2c.8511A>G (p.Gly2837=)
c.8142A>G (p.Gly2714=)
c.978A>G (p.Gly326=)
c.8519A>G (n.8519A>G)
c.1076A>G
c.9A>G (p.Gly3=)
c.8415A>G (p.Gly2805=)
 ClinVar dbSNP
13g.32370979A>TCA483261503BRCA2c.8511A>T (p.Gly2837=)
c.8142A>T (p.Gly2714=)
c.978A>T (p.Gly326=)
c.8519A>T (n.8519A>T)
c.1076A>T
c.9A>T (p.Gly3=)
c.8415A>T (p.Gly2805=)
13g.32370980T>ACA387752701BRCA2c.8512T>A (p.Leu2838Ile)
c.8143T>A (p.Leu2715Ile)
c.979T>A (p.Leu327Ile)
c.8520T>A (n.8520T>A)
c.1077T>A
c.10T>A (p.Leu4Ile)
c.8416T>A (p.Leu2806Ile)
 dbSNP
13g.32370980T>CCA483261504BRCA2c.8512T>C (p.Leu2838=)
c.8143T>C (p.Leu2715=)
c.979T>C (p.Leu327=)
c.8520T>C (n.8520T>C)
c.1077T>C
c.10T>C (p.Leu4=)
c.8416T>C (p.Leu2806=)
13g.32370980T>GCA387752702BRCA2c.8512T>G (p.Leu2838Val)
c.8143T>G (p.Leu2715Val)
c.979T>G (p.Leu327Val)
c.8520T>G (n.8520T>G)
c.1077T>G
c.10T>G (p.Leu4Val)
c.8416T>G (p.Leu2806Val)
13g.32370981delCA2727920447BRCA2c.8513del (p.Leu2838TyrfsTer25)
c.8144del (p.Leu2715TyrfsTer25)
c.980del (p.Leu327TyrfsTer25)
c.8521del (n.8521del)
c.1078del
c.11del (p.Leu4TyrfsTer25)
c.8417del (p.Leu2806TyrfsTer25)
 dbSNP
13g.32370980_32370982delinsTTACA2082815465BRCA2c.8512_8514delinsTTA (p.Leu2838=)
c.8143_8145delinsTTA (p.Leu2715=)
c.979_981delinsTTA (p.Leu327=)
c.8520_8522delinsTTA (n.8520_8522delinsTTA)
c.1077_1079delinsTTA
c.10_12delinsTTA (p.Leu4=)
c.8416_8418delinsTTA (p.Leu2806=)
13g.32370981T>ACA10589502BRCA2c.8513T>A (p.Leu2838Ter)
c.8144T>A (p.Leu2715Ter)
c.980T>A (p.Leu327Ter)
c.8521T>A (n.8521T>A)
c.1078T>A
c.11T>A (p.Leu4Ter)
c.8417T>A (p.Leu2806Ter)
 ClinVar dbSNP
13g.32370981T>CCA387752703BRCA2c.8513T>C (p.Leu2838Ser)
c.8144T>C (p.Leu2715Ser)
c.980T>C (p.Leu327Ser)
c.8521T>C (n.8521T>C)
c.1078T>C
c.11T>C (p.Leu4Ser)
c.8417T>C (p.Leu2806Ser)
13g.32370981T>GCA10589503BRCA2c.8513T>G (p.Leu2838Ter)
c.8144T>G (p.Leu2715Ter)
c.980T>G (p.Leu327Ter)
c.8521T>G (n.8521T>G)
c.1078T>G
c.11T>G (p.Leu4Ter)
c.8417T>G (p.Leu2806Ter)
 ClinVar dbSNP
13g.32370981T=CA2082815473BRCA2c.8513T= (p.Leu2838=)
c.8144T= (p.Leu2715=)
c.980T= (p.Leu327=)
c.8521T= (n.8521T=)
c.1078T=
c.11T= (p.Leu4=)
c.8417T= (p.Leu2806=)
13g.32370983_32370984delCA891843899BRCA2c.8515_8516del (p.Tyr2839HisfsTer5)
c.8146_8147del (p.Tyr2716HisfsTer5)
c.982_983del (p.Tyr328HisfsTer5)
c.8523_8524del (n.8523_8524del)
c.1080_1081del
c.13_14del (p.Tyr5HisfsTer5)
c.8419_8420del (p.Tyr2807HisfsTer5)
 ClinVar dbSNP
13g.32370982A=CA2082815482BRCA2c.8514A= (p.Leu2838=)
c.8145A= (p.Leu2715=)
c.981A= (p.Leu327=)
c.8522A= (n.8522A=)
c.1079A=
c.12A= (p.Leu4=)
c.8418A= (p.Leu2806=)
13g.32370982A>CCA387752704BRCA2c.8514A>C (p.Leu2838Phe)
c.8145A>C (p.Leu2715Phe)
c.981A>C (p.Leu327Phe)
c.8522A>C (n.8522A>C)
c.1079A>C
c.12A>C (p.Leu4Phe)
c.8418A>C (p.Leu2806Phe)
13g.32370982A>GCA6941255BRCA2c.8514A>G (p.Leu2838=)
c.8145A>G (p.Leu2715=)
c.981A>G (p.Leu327=)
c.8522A>G (n.8522A>G)
c.1079A>G
c.12A>G (p.Leu4=)
c.8418A>G (p.Leu2806=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32370982A>TCA387752705BRCA2c.8514A>T (p.Leu2838Phe)
c.8145A>T (p.Leu2715Phe)
c.981A>T (p.Leu327Phe)
c.8522A>T (n.8522A>T)
c.1079A>T
c.12A>T (p.Leu4Phe)
c.8418A>T (p.Leu2806Phe)
13g.32370983T>ACA387752706BRCA2c.8515T>A (p.Tyr2839Asn)
c.8146T>A (p.Tyr2716Asn)
c.982T>A (p.Tyr328Asn)
c.8523T>A (n.8523T>A)
c.1080T>A
c.13T>A (p.Tyr5Asn)
c.8419T>A (p.Tyr2807Asn)
13g.32370983T>CCA025688BRCA2c.8515T>C (p.Tyr2839His)
c.8146T>C (p.Tyr2716His)
c.982T>C (p.Tyr328His)
c.8523T>C (n.8523T>C)
c.1080T>C
c.13T>C (p.Tyr5His)
c.8419T>C (p.Tyr2807His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32370983T>GCA387752707BRCA2c.8515T>G (p.Tyr2839Asp)
c.8146T>G (p.Tyr2716Asp)
c.982T>G (p.Tyr328Asp)
c.8523T>G (n.8523T>G)
c.1080T>G
c.13T>G (p.Tyr5Asp)
c.8419T>G (p.Tyr2807Asp)
13g.32370983T=CA2082815501BRCA2c.8515T= (p.Tyr2839=)
c.8146T= (p.Tyr2716=)
c.982T= (p.Tyr328=)
c.8523T= (n.8523T=)
c.1080T=
c.13T= (p.Tyr5=)
c.8419T= (p.Tyr2807=)
13g.32370984A=CA2082815505BRCA2c.8516A= (p.Tyr2839=)
c.8147A= (p.Tyr2716=)
c.983A= (p.Tyr328=)
c.8524A= (n.8524A=)
c.1081A=
c.14A= (p.Tyr5=)
c.8420A= (p.Tyr2807=)
13g.32370984A>CCA387752708BRCA2c.8516A>C (p.Tyr2839Ser)
c.8147A>C (p.Tyr2716Ser)
c.983A>C (p.Tyr328Ser)
c.8524A>C (n.8524A>C)
c.1081A>C
c.14A>C (p.Tyr5Ser)
c.8420A>C (p.Tyr2807Ser)
13g.32370984A>GCA025689BRCA2c.8516A>G (p.Tyr2839Cys)
c.8147A>G (p.Tyr2716Cys)
c.983A>G (p.Tyr328Cys)
c.8524A>G (n.8524A>G)
c.1081A>G
c.14A>G (p.Tyr5Cys)
c.8420A>G (p.Tyr2807Cys)
 ClinVar dbSNP
13g.32370984A>TCA387752709BRCA2c.8516A>T (p.Tyr2839Phe)
c.8147A>T (p.Tyr2716Phe)
c.983A>T (p.Tyr328Phe)
c.8524A>T (n.8524A>T)
c.1081A>T
c.14A>T (p.Tyr5Phe)
c.8420A>T (p.Tyr2807Phe)
 dbSNP
13g.32370985C>ACA10589504BRCA2c.8517C>A (p.Tyr2839Ter)
c.8148C>A (p.Tyr2716Ter)
c.984C>A (p.Tyr328Ter)
c.8525C>A (n.8525C>A)
c.1082C>A
c.15C>A (p.Tyr5Ter)
c.8421C>A (p.Tyr2807Ter)
 ClinVar dbSNP
13g.32370985C=CA2082815514BRCA2c.8517C= (p.Tyr2839=)
c.8148C= (p.Tyr2716=)
c.984C= (p.Tyr328=)
c.8525C= (n.8525C=)
c.1082C=
c.15C= (p.Tyr5=)
c.8421C= (p.Tyr2807=)
13g.32370985C>GCA387752710BRCA2c.8517C>G (p.Tyr2839Ter)
c.8148C>G (p.Tyr2716Ter)
c.984C>G (p.Tyr328Ter)
c.8525C>G (n.8525C>G)
c.1082C>G
c.15C>G (p.Tyr5Ter)
c.8421C>G (p.Tyr2807Ter)
 ClinVar dbSNP
13g.32370985C>TCA337412BRCA2c.8517C>T (p.Tyr2839=)
c.8148C>T (p.Tyr2716=)
c.984C>T (p.Tyr328=)
c.8525C>T (n.8525C>T)
c.1082C>T
c.15C>T (p.Tyr5=)
c.8421C>T (p.Tyr2807=)
 ClinVar dbSNP
13g.32370985_32370986delinsCACA2082815520BRCA2c.8517_8518delinsCA (p.Tyr2839=)
c.8148_8149delinsCA (p.Tyr2716=)
c.984_985delinsCA (p.Tyr328=)
c.8525_8526delinsCA (n.8525_8526delinsCA)
c.1082_1083delinsCA
c.15_16delinsCA (p.Tyr5=)
c.8421_8422delinsCA (p.Tyr2807=)
13g.32370986delCA10589505BRCA2c.8518del (p.Ile2840TyrfsTer23)
c.8149del (p.Ile2717TyrfsTer23)
c.985del (p.Ile329TyrfsTer23)
c.8526del (n.8526del)
c.1083del
c.16del (p.Ile6TyrfsTer23)
c.8422del (p.Ile2808TyrfsTer23)
 ClinVar dbSNP
13g.32370986A=CA2082815528BRCA2c.8518A= (p.Ile2840=)
c.8149A= (p.Ile2717=)
c.985A= (p.Ile329=)
c.8526A= (n.8526A=)
c.1083A=
c.16A= (p.Ile6=)
c.8422A= (p.Ile2808=)
13g.32370986A>CCA387752711BRCA2c.8518A>C (p.Ile2840Leu)
c.8149A>C (p.Ile2717Leu)
c.985A>C (p.Ile329Leu)
c.8526A>C (n.8526A>C)
c.1083A>C
c.16A>C (p.Ile6Leu)
c.8422A>C (p.Ile2808Leu)
13g.32370986A>GCA025690BRCA2c.8518A>G (p.Ile2840Val)
c.8149A>G (p.Ile2717Val)
c.985A>G (p.Ile329Val)
c.8526A>G (n.8526A>G)
c.1083A>G
c.16A>G (p.Ile6Val)
c.8422A>G (p.Ile2808Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32370986A>TCA387752712BRCA2c.8518A>T (p.Ile2840Leu)
c.8149A>T (p.Ile2717Leu)
c.985A>T (p.Ile329Leu)
c.8526A>T (n.8526A>T)
c.1083A>T
c.16A>T (p.Ile6Leu)
c.8422A>T (p.Ile2808Leu)
13g.32370987T>ACA387752713BRCA2c.8519T>A (p.Ile2840Lys)
c.8150T>A (p.Ile2717Lys)
c.986T>A (p.Ile329Lys)
c.8527T>A (n.8527T>A)
c.1084T>A
c.17T>A (p.Ile6Lys)
c.8423T>A (p.Ile2808Lys)
 dbSNP
13g.32370987T>CCA387752714BRCA2c.8519T>C (p.Ile2840Thr)
c.8150T>C (p.Ile2717Thr)
c.986T>C (p.Ile329Thr)
c.8527T>C (n.8527T>C)
c.1084T>C
c.17T>C (p.Ile6Thr)
c.8423T>C (p.Ile2808Thr)
 ClinVar dbSNP gnomAD v4
13g.32370987T>GCA387752715BRCA2c.8519T>G (p.Ile2840Arg)
c.8150T>G (p.Ile2717Arg)
c.986T>G (p.Ile329Arg)
c.8527T>G (n.8527T>G)
c.1084T>G
c.17T>G (p.Ile6Arg)
c.8423T>G (p.Ile2808Arg)
13g.32370987T=CA2082815535BRCA2c.8519T= (p.Ile2840=)
c.8150T= (p.Ile2717=)
c.986T= (p.Ile329=)
c.8527T= (n.8527T=)
c.1084T=
c.17T= (p.Ile6=)
c.8423T= (p.Ile2808=)
13g.32370988A=CA2082815543BRCA2c.8520A= (p.Ile2840=)
c.8151A= (p.Ile2717=)
c.987A= (p.Ile329=)
c.8528A= (n.8528A=)
c.1085A=
c.18A= (p.Ile6=)
c.8424A= (p.Ile2808=)
13g.32370988A>CCA6941256BRCA2c.8520A>C (p.Ile2840=)
c.8151A>C (p.Ile2717=)
c.987A>C (p.Ile329=)
c.8528A>C (n.8528A>C)
c.1085A>C
c.18A>C (p.Ile6=)
c.8424A>C (p.Ile2808=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32370988A>GCA387752716BRCA2c.8520A>G (p.Ile2840Met)
c.8151A>G (p.Ile2717Met)
c.987A>G (p.Ile329Met)
c.8528A>G (n.8528A>G)
c.1085A>G
c.18A>G (p.Ile6Met)
c.8424A>G (p.Ile2808Met)
 dbSNP
13g.32370988A>TCA483261505BRCA2c.8520A>T (p.Ile2840=)
c.8151A>T (p.Ile2717=)
c.987A>T (p.Ile329=)
c.8528A>T (n.8528A>T)
c.1085A>T
c.18A>T (p.Ile6=)
c.8424A>T (p.Ile2808=)
 dbSNP
13g.32370989T>ACA387752717BRCA2c.8521T>A (p.Phe2841Ile)
c.8152T>A (p.Phe2718Ile)
c.988T>A (p.Phe330Ile)
c.8529T>A (n.8529T>A)
c.1086T>A
c.19T>A (p.Phe7Ile)
c.8425T>A (p.Phe2809Ile)
 ClinVar dbSNP COSMIC COSMIC
13g.32370989T>CCA387752718BRCA2c.8521T>C (p.Phe2841Leu)
c.8152T>C (p.Phe2718Leu)
c.988T>C (p.Phe330Leu)
c.8529T>C (n.8529T>C)
c.1086T>C
c.19T>C (p.Phe7Leu)
c.8425T>C (p.Phe2809Leu)
 ClinVar
13g.32370989T>GCA387752719BRCA2c.8521T>G (p.Phe2841Val)
c.8152T>G (p.Phe2718Val)
c.988T>G (p.Phe330Val)
c.8529T>G (n.8529T>G)
c.1086T>G
c.19T>G (p.Phe7Val)
c.8425T>G (p.Phe2809Val)
13g.32370991delCA2499222335BRCA2c.8523del (p.Arg2842AlafsTer21)
c.8154del (p.Arg2719AlafsTer21)
c.990del (p.Arg331AlafsTer21)
c.8531del (n.8531del)
c.1088del
c.21del (p.Arg8AlafsTer21)
c.8427del (p.Arg2810AlafsTer21)
 ClinVar dbSNP
13g.32370990T>ACA387752720BRCA2c.8522T>A (p.Phe2841Tyr)
c.8153T>A (p.Phe2718Tyr)
c.989T>A (p.Phe330Tyr)
c.8530T>A (n.8530T>A)
c.1087T>A
c.20T>A (p.Phe7Tyr)
c.8426T>A (p.Phe2809Tyr)
 dbSNP
13g.32370990T>CCA387752721BRCA2c.8522T>C (p.Phe2841Ser)
c.8153T>C (p.Phe2718Ser)
c.989T>C (p.Phe330Ser)
c.8530T>C (n.8530T>C)
c.1087T>C
c.20T>C (p.Phe7Ser)
c.8426T>C (p.Phe2809Ser)
 dbSNP
13g.32370990T>GCA387752722BRCA2c.8522T>G (p.Phe2841Cys)
c.8153T>G (p.Phe2718Cys)
c.989T>G (p.Phe330Cys)
c.8530T>G (n.8530T>G)
c.1087T>G
c.20T>G (p.Phe7Cys)
c.8426T>G (p.Phe2809Cys)
13g.32370991T>ACA387752724BRCA2c.8523T>A (p.Phe2841Leu)
c.8154T>A (p.Phe2718Leu)
c.990T>A (p.Phe330Leu)
c.8531T>A (n.8531T>A)
c.1088T>A
c.21T>A (p.Phe7Leu)
c.8427T>A (p.Phe2809Leu)
 dbSNP
13g.32370991T>CCA483261506BRCA2c.8523T>C (p.Phe2841=)
c.8154T>C (p.Phe2718=)
c.990T>C (p.Phe330=)
c.8531T>C (n.8531T>C)
c.1088T>C
c.21T>C (p.Phe7=)
c.8427T>C (p.Phe2809=)
13g.32370991T>GCA387752723BRCA2c.8523T>G (p.Phe2841Leu)
c.8154T>G (p.Phe2718Leu)
c.990T>G (p.Phe330Leu)
c.8531T>G (n.8531T>G)
c.1088T>G
c.21T>G (p.Phe7Leu)
c.8427T>G (p.Phe2809Leu)
 gnomAD v4
13g.32370992C>ACA387752725BRCA2c.8524C>A (p.Arg2842Ser)
c.8155C>A (p.Arg2719Ser)
c.991C>A (p.Arg331Ser)
c.8532C>A (n.8532C>A)
c.1089C>A
c.22C>A (p.Arg8Ser)
c.8428C>A (p.Arg2810Ser)
 ClinVar dbSNP
13g.32370992C=CA2082815559BRCA2c.8524C= (p.Arg2842=)
c.8155C= (p.Arg2719=)
c.991C= (p.Arg331=)
c.8532C= (n.8532C=)
c.1089C=
c.22C= (p.Arg8=)
c.8428C= (p.Arg2810=)
13g.32370992C>GCA387752726BRCA2c.8524C>G (p.Arg2842Gly)
c.8155C>G (p.Arg2719Gly)
c.991C>G (p.Arg331Gly)
c.8532C>G (n.8532C>G)
c.1089C>G
c.22C>G (p.Arg8Gly)
c.8428C>G (p.Arg2810Gly)
 ClinVar dbSNP gnomAD v4
13g.32370992C>TCA025691BRCA2c.8524C>T (p.Arg2842Cys)
c.8155C>T (p.Arg2719Cys)
c.991C>T (p.Arg331Cys)
c.8532C>T (n.8532C>T)
c.1089C>T
c.22C>T (p.Arg8Cys)
c.8428C>T (p.Arg2810Cys)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32370993G>ACA025692BRCA2c.8525G>A (p.Arg2842His)
c.8156G>A (p.Arg2719His)
c.992G>A (p.Arg331His)
c.8533G>A (n.8533G>A)
c.1090G>A
c.23G>A (p.Arg8His)
c.8429G>A (p.Arg2810His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32370993G>CCA387752727BRCA2c.8525G>C (p.Arg2842Pro)
c.8156G>C (p.Arg2719Pro)
c.992G>C (p.Arg331Pro)
c.8533G>C (n.8533G>C)
c.1090G>C
c.23G>C (p.Arg8Pro)
c.8429G>C (p.Arg2810Pro)
 dbSNP gnomAD v4
13g.32370993G=CA2082815570BRCA2c.8525G= (p.Arg2842=)
c.8156G= (p.Arg2719=)
c.992G= (p.Arg331=)
c.8533G= (n.8533G=)
c.1090G=
c.23G= (p.Arg8=)
c.8429G= (p.Arg2810=)
13g.32370993G>TCA025693BRCA2c.8525G>T (p.Arg2842Leu)
c.8156G>T (p.Arg2719Leu)
c.992G>T (p.Arg331Leu)
c.8533G>T (n.8533G>T)
c.1090G>T
c.23G>T (p.Arg8Leu)
c.8429G>T (p.Arg2810Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32370994C>ACA483261509BRCA2c.8526C>A (p.Arg2842=)
c.8157C>A (p.Arg2719=)
c.993C>A (p.Arg331=)
c.8534C>A (n.8534C>A)
c.1091C>A
c.24C>A (p.Arg8=)
c.8430C>A (p.Arg2810=)
13g.32370994C=CA2082815578BRCA2c.8526C= (p.Arg2842=)
c.8157C= (p.Arg2719=)
c.993C= (p.Arg331=)
c.8534C= (n.8534C=)
c.1091C=
c.24C= (p.Arg8=)
c.8430C= (p.Arg2810=)
13g.32370994C>GCA483261508BRCA2c.8526C>G (p.Arg2842=)
c.8157C>G (p.Arg2719=)
c.993C>G (p.Arg331=)
c.8534C>G (n.8534C>G)
c.1091C>G
c.24C>G (p.Arg8=)
c.8430C>G (p.Arg2810=)
13g.32370994C>TCA483261507BRCA2c.8526C>T (p.Arg2842=)
c.8157C>T (p.Arg2719=)
c.993C>T (p.Arg331=)
c.8534C>T (n.8534C>T)
c.1091C>T
c.24C>T (p.Arg8=)
c.8430C>T (p.Arg2810=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32370994_32370995delinsCACA2082815577BRCA2c.8526_8527delinsCA (p.Arg2842=)
c.8157_8158delinsCA (p.Arg2719=)
c.993_994delinsCA (p.Arg331=)
c.8534_8535delinsCA (n.8534_8535delinsCA)
c.1091_1092delinsCA
c.24_25delinsCA (p.Arg8=)
c.8430_8431delinsCA (p.Arg2810=)
13g.32370995A=CA2082815588BRCA2c.8527A= (p.Asn2843=)
c.8158A= (p.Asn2720=)
c.994A= (p.Asn332=)
c.8535A= (n.8535A=)
c.1092A=
c.25A= (p.Asn9=)
c.8431A= (p.Asn2811=)
13g.32370995A>CCA387752728BRCA2c.8527A>C (p.Asn2843His)
c.8158A>C (p.Asn2720His)
c.994A>C (p.Asn332His)
c.8535A>C (n.8535A>C)
c.1092A>C
c.25A>C (p.Asn9His)
c.8431A>C (p.Asn2811His)
 ClinVar dbSNP gnomAD v4
13g.32370995A>GCA10579792BRCA2c.8527A>G (p.Asn2843Asp)
c.8158A>G (p.Asn2720Asp)
c.994A>G (p.Asn332Asp)
c.8535A>G (n.8535A>G)
c.1092A>G
c.25A>G (p.Asn9Asp)
c.8431A>G (p.Asn2811Asp)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32370995A>TCA387752729BRCA2c.8527A>T (p.Asn2843Tyr)
c.8158A>T (p.Asn2720Tyr)
c.994A>T (p.Asn332Tyr)
c.8535A>T (n.8535A>T)
c.1092A>T
c.25A>T (p.Asn9Tyr)
c.8431A>T (p.Asn2811Tyr)
13g.32370996delCA025695BRCA2c.8528del (p.Asn2843MetfsTer20)
c.8159del (p.Asn2720MetfsTer20)
c.995del (p.Asn332MetfsTer20)
c.8536del (n.8536del)
c.1093del
c.26del (p.Asn9MetfsTer20)
c.8432del (p.Asn2811MetfsTer20)
 ClinVar dbSNP
13g.32370996A=CA2082815601BRCA2c.8528A= (p.Asn2843=)
c.8159A= (p.Asn2720=)
c.995A= (p.Asn332=)
c.8536A= (n.8536A=)
c.1093A=
c.26A= (p.Asn9=)
c.8432A= (p.Asn2811=)
13g.32370996A>CCA387752730BRCA2c.8528A>C (p.Asn2843Thr)
c.8159A>C (p.Asn2720Thr)
c.995A>C (p.Asn332Thr)
c.8536A>C (n.8536A>C)
c.1093A>C
c.26A>C (p.Asn9Thr)
c.8432A>C (p.Asn2811Thr)
13g.32370996A>GCA025694BRCA2c.8528A>G (p.Asn2843Ser)
c.8159A>G (p.Asn2720Ser)
c.995A>G (p.Asn332Ser)
c.8536A>G (n.8536A>G)
c.1093A>G
c.26A>G (p.Asn9Ser)
c.8432A>G (p.Asn2811Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32370996A>TCA387752731BRCA2c.8528A>T (p.Asn2843Ile)
c.8159A>T (p.Asn2720Ile)
c.995A>T (p.Asn332Ile)
c.8536A>T (n.8536A>T)
c.1093A>T
c.26A>T (p.Asn9Ile)
c.8432A>T (p.Asn2811Ile)
 dbSNP
13g.32370997T>ACA387752733BRCA2c.8529T>A (p.Asn2843Lys)
c.8160T>A (p.Asn2720Lys)
c.996T>A (p.Asn332Lys)
c.8537T>A (n.8537T>A)
c.1094T>A
c.27T>A (p.Asn9Lys)
c.8433T>A (p.Asn2811Lys)
 dbSNP
13g.32370997T>CCA483261510BRCA2c.8529T>C (p.Asn2843=)
c.8160T>C (p.Asn2720=)
c.996T>C (p.Asn332=)
c.8537T>C (n.8537T>C)
c.1094T>C
c.27T>C (p.Asn9=)
c.8433T>C (p.Asn2811=)
 ClinVar dbSNP COSMIC COSMIC
13g.32370997T>GCA387752732BRCA2c.8529T>G (p.Asn2843Lys)
c.8160T>G (p.Asn2720Lys)
c.996T>G (p.Asn332Lys)
c.8537T>G (n.8537T>G)
c.1094T>G
c.27T>G (p.Asn9Lys)
c.8433T>G (p.Asn2811Lys)
13g.32370997T=CA2082815606BRCA2c.8529T= (p.Asn2843=)
c.8160T= (p.Asn2720=)
c.996T= (p.Asn332=)
c.8537T= (n.8537T=)
c.1094T=
c.27T= (p.Asn9=)
c.8433T= (p.Asn2811=)
13g.32370998G>ACA6941257BRCA2c.8530G>A (p.Glu2844Lys)
c.8161G>A (p.Glu2721Lys)
c.997G>A (p.Glu333Lys)
c.8538G>A (n.8538G>A)
c.1095G>A
c.28G>A (p.Glu10Lys)
c.8434G>A (p.Glu2812Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32370998G>CCA387752735BRCA2c.8530G>C (p.Glu2844Gln)
c.8161G>C (p.Glu2721Gln)
c.997G>C (p.Glu333Gln)
c.8538G>C (n.8538G>C)
c.1095G>C
c.28G>C (p.Glu10Gln)
c.8434G>C (p.Glu2812Gln)
13g.32370998G=CA2082815616BRCA2c.8530G= (p.Glu2844=)
c.8161G= (p.Glu2721=)
c.997G= (p.Glu333=)
c.8538G= (n.8538G=)
c.1095G=
c.28G= (p.Glu10=)
c.8434G= (p.Glu2812=)
13g.32370998G>TCA387752734BRCA2c.8530G>T (p.Glu2844Ter)
c.8161G>T (p.Glu2721Ter)
c.997G>T (p.Glu333Ter)
c.8538G>T (n.8538G>T)
c.1095G>T
c.28G>T (p.Glu10Ter)
c.8434G>T (p.Glu2812Ter)
13g.32370998_32371000delinsGAACA2082815615BRCA2c.8530_8532delinsGAA (p.Glu2844=)
c.8161_8163delinsGAA (p.Glu2721=)
c.997_999delinsGAA (p.Glu333=)
c.8538_8540delinsGAA (n.8538_8540delinsGAA)
c.1095_1097delinsGAA
c.28_30delinsGAA (p.Glu10=)
c.8434_8436delinsGAA (p.Glu2812=)
13g.32370999A=CA2082815637BRCA2c.8531A= (p.Glu2844=)
c.8162A= (p.Glu2721=)
c.998A= (p.Glu333=)
c.8539A= (n.8539A=)
c.1096A=
c.29A= (p.Glu10=)
c.8435A= (p.Glu2812=)
13g.32370999A>CCA387752736BRCA2c.8531A>C (p.Glu2844Ala)
c.8162A>C (p.Glu2721Ala)
c.998A>C (p.Glu333Ala)
c.8539A>C (n.8539A>C)
c.1096A>C
c.29A>C (p.Glu10Ala)
c.8435A>C (p.Glu2812Ala)
 ClinVar dbSNP
13g.32370999A>GCA247484126BRCA2c.8531A>G (p.Glu2844Gly)
c.8162A>G (p.Glu2721Gly)
c.998A>G (p.Glu333Gly)
c.8539A>G (n.8539A>G)
c.1096A>G
c.29A>G (p.Glu10Gly)
c.8435A>G (p.Glu2812Gly)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32370999A>TCA387752737BRCA2c.8531A>T (p.Glu2844Val)
c.8162A>T (p.Glu2721Val)
c.998A>T (p.Glu333Val)
c.8539A>T (n.8539A>T)
c.1096A>T
c.29A>T (p.Glu10Val)
c.8435A>T (p.Glu2812Val)
13g.32371001dupCA645509336BRCA2c.8533dup (p.Arg2845LysfsTer24)
c.8164dup (p.Arg2722LysfsTer24)
c.1000dup (p.Arg334LysfsTer24)
c.8541dup (n.8541dup)
c.1098dup
c.31dup (p.Arg11LysfsTer24)
c.8437dup (p.Arg2813LysfsTer24)
 ClinVar dbSNP
13g.32371001delCA2695199703BRCA2c.8533del (p.Arg2845GlufsTer18)
c.8164del (p.Arg2722GlufsTer18)
c.1000del (p.Arg334GlufsTer18)
c.8541del (n.8541del)
c.1098del
c.31del (p.Arg11GlufsTer18)
c.8437del (p.Arg2813GlufsTer18)
 ClinVar
13g.32371000_32371001delCA025696BRCA2c.8532_8533del (p.Glu2846GlyfsTer22)
c.8163_8164del (p.Glu2723GlyfsTer22)
c.999_1000del (p.Glu335GlyfsTer22)
c.8540_8541del (n.8540_8541del)
c.1097_1098del
c.30_31del (p.Glu12GlyfsTer22)
c.8436_8437del (p.Glu2814GlyfsTer22)
 ClinVar dbSNP gnomAD v4
13g.32371000_32371014delCA2697551753BRCA2c.8532_8546del (p.Arg2845_Lys2849del)
c.8163_8177del (p.Arg2722_Lys2726del)
c.999_1013del (p.Arg334_Lys338del)
c.8540_8554del (n.8540_8554del)
c.1097_1111del
c.30_44del (p.Arg11_Lys15del)
c.8436_8450del (p.Arg2813_Lys2817del)
 ClinVar
13g.32371000A>CCA387752738BRCA2c.8532A>C (p.Glu2844Asp)
c.8163A>C (p.Glu2721Asp)
c.999A>C (p.Glu333Asp)
c.8540A>C (n.8540A>C)
c.1097A>C
c.30A>C (p.Glu10Asp)
c.8436A>C (p.Glu2812Asp)
13g.32371000A>GCA483261511BRCA2c.8532A>G (p.Glu2844=)
c.8163A>G (p.Glu2721=)
c.999A>G (p.Glu333=)
c.8540A>G (n.8540A>G)
c.1097A>G
c.30A>G (p.Glu10=)
c.8436A>G (p.Glu2812=)
 gnomAD v4
13g.32371000A>TCA387752739BRCA2c.8532A>T (p.Glu2844Asp)
c.8163A>T (p.Glu2721Asp)
c.999A>T (p.Glu333Asp)
c.8540A>T (n.8540A>T)
c.1097A>T
c.30A>T (p.Glu10Asp)
c.8436A>T (p.Glu2812Asp)
13g.32371000_32371004delinsAAGAGCA2082815646BRCA2c.8532_8536delinsAAGAG (p.Glu2844=)
c.8163_8167delinsAAGAG (p.Glu2721=)
c.999_1003delinsAAGAG (p.Glu333=)
c.8540_8544delinsAAGAG (n.8540_8544delinsAAGAG)
c.1097_1101delinsAAGAG
c.30_34delinsAAGAG (p.Glu10=)
c.8436_8440delinsAAGAG (p.Glu2812=)
13g.32371001A>CCA483261512BRCA2c.8533A>C (p.Arg2845=)
c.8164A>C (p.Arg2722=)
c.1000A>C (p.Arg334=)
c.8541A>C (n.8541A>C)
c.1098A>C
c.31A>C (p.Arg11=)
c.8437A>C (p.Arg2813=)
13g.32371001A>GCA387752740BRCA2c.8533A>G (p.Arg2845Gly)
c.8164A>G (p.Arg2722Gly)
c.1000A>G (p.Arg334Gly)
c.8541A>G (n.8541A>G)
c.1098A>G
c.31A>G (p.Arg11Gly)
c.8437A>G (p.Arg2813Gly)
 dbSNP
13g.32371001A>TCA387752741BRCA2c.8533A>T (p.Arg2845Ter)
c.8164A>T (p.Arg2722Ter)
c.1000A>T (p.Arg334Ter)
c.8541A>T (n.8541A>T)
c.1098A>T
c.31A>T (p.Arg11Ter)
c.8437A>T (p.Arg2813Ter)
13g.32371005_32371006delCA025697BRCA2c.8537_8538del (p.Glu2846GlyfsTer22)
c.8168_8169del (p.Glu2723GlyfsTer22)
c.1004_1005del (p.Glu335GlyfsTer22)
c.8545_8546del (n.8545_8546del)
c.1102_1103del
c.35_36del (p.Glu12GlyfsTer22)
c.8441_8442del (p.Glu2814GlyfsTer22)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32371003_32371006delCA025698BRCA2c.8535_8538del (p.Glu2846LysfsTer16)
c.8166_8169del (p.Glu2723LysfsTer16)
c.1002_1005del (p.Glu335LysfsTer16)
c.8543_8546del (n.8543_8546del)
c.1100_1103del
c.33_36del (p.Glu12LysfsTer16)
c.8439_8442del (p.Glu2814LysfsTer16)
 ClinVar dbSNP gnomAD v4
13g.32371002G>ACA387752742BRCA2c.8534G>A (p.Arg2845Lys)
c.8165G>A (p.Arg2722Lys)
c.1001G>A (p.Arg334Lys)
c.8542G>A (n.8542G>A)
c.1099G>A
c.32G>A (p.Arg11Lys)
c.8438G>A (p.Arg2813Lys)
 ClinVar
13g.32371002G>CCA387752743BRCA2c.8534G>C (p.Arg2845Thr)
c.8165G>C (p.Arg2722Thr)
c.1001G>C (p.Arg334Thr)
c.8542G>C (n.8542G>C)
c.1099G>C
c.32G>C (p.Arg11Thr)
c.8438G>C (p.Arg2813Thr)
13g.32371002G>TCA387752744BRCA2c.8534G>T (p.Arg2845Ile)
c.8165G>T (p.Arg2722Ile)
c.1001G>T (p.Arg334Ile)
c.8542G>T (n.8542G>T)
c.1099G>T
c.32G>T (p.Arg11Ile)
c.8438G>T (p.Arg2813Ile)
13g.32371002_32371003insTCGCCA2538391578BRCA2c.8534_8535insTCGC (p.Arg2845SerfsTer25)
c.8165_8166insTCGC (p.Arg2722SerfsTer25)
c.1001_1002insTCGC (p.Arg334SerfsTer25)
c.8542_8543insTCGC (n.8542_8543insTCGC)
c.1099_1100insTCGC
c.32_33insTCGC (p.Arg11SerfsTer25)
c.8438_8439insTCGC (p.Arg2813SerfsTer25)
13g.32371003delCA2575388009BRCA2c.8535del (p.Glu2846ArgfsTer17)
c.8166del (p.Glu2723ArgfsTer17)
c.1002del (p.Glu335ArgfsTer17)
c.8543del (n.8543del)
c.1100del
c.33del (p.Glu12ArgfsTer17)
c.8439del (p.Glu2814ArgfsTer17)
 ClinVar
13g.32371003A>CCA387752745BRCA2c.8535A>C (p.Arg2845Ser)
c.8166A>C (p.Arg2722Ser)
c.1002A>C (p.Arg334Ser)
c.8543A>C (n.8543A>C)
c.1100A>C
c.33A>C (p.Arg11Ser)
c.8439A>C (p.Arg2813Ser)
13g.32371003A>GCA483261513BRCA2c.8535A>G (p.Arg2845=)
c.8166A>G (p.Arg2722=)
c.1002A>G (p.Arg334=)
c.8543A>G (n.8543A>G)
c.1100A>G
c.33A>G (p.Arg11=)
c.8439A>G (p.Arg2813=)
13g.32371003A>TCA387752746BRCA2c.8535A>T (p.Arg2845Ser)
c.8166A>T (p.Arg2722Ser)
c.1002A>T (p.Arg334Ser)
c.8543A>T (n.8543A>T)
c.1100A>T
c.33A>T (p.Arg11Ser)
c.8439A>T (p.Arg2813Ser)
 dbSNP
13g.32371004G>ACA387752748BRCA2c.8536G>A (p.Glu2846Lys)
c.8167G>A (p.Glu2723Lys)
c.1003G>A (p.Glu335Lys)
c.8544G>A (n.8544G>A)
c.1101G>A
c.34G>A (p.Glu12Lys)
c.8440G>A (p.Glu2814Lys)
 dbSNP
13g.32371004G>CCA387752747BRCA2c.8536G>C (p.Glu2846Gln)
c.8167G>C (p.Glu2723Gln)
c.1003G>C (p.Glu335Gln)
c.8544G>C (n.8544G>C)
c.1101G>C
c.34G>C (p.Glu12Gln)
c.8440G>C (p.Glu2814Gln)
 dbSNP gnomAD v3 gnomAD v4
13g.32371004G=CA2082815654BRCA2c.8536G= (p.Glu2846=)
c.8167G= (p.Glu2723=)
c.1003G= (p.Glu335=)
c.8544G= (n.8544G=)
c.1101G=
c.34G= (p.Glu12=)
c.8440G= (p.Glu2814=)
13g.32371004G>TCA10589506BRCA2c.8536G>T (p.Glu2846Ter)
c.8167G>T (p.Glu2723Ter)
c.1003G>T (p.Glu335Ter)
c.8544G>T (n.8544G>T)
c.1101G>T
c.34G>T (p.Glu12Ter)
c.8440G>T (p.Glu2814Ter)
 ClinVar dbSNP
13g.32371004_32371005insCATATCACCCA2525526208BRCA2c.8536_8537insCATATCACC (p.Glu2846delinsAlaTyrHisGln)
c.8167_8168insCATATCACC (p.Glu2723delinsAlaTyrHisGln)
c.1003_1004insCATATCACC (p.Glu335delinsAlaTyrHisGln)
c.8544_8545insCATATCACC (n.8544_8545insCATATCACC)
c.1101_1102insCATATCACC
c.34_35insCATATCACC (p.Glu12delinsAlaTyrHisGln)
c.8440_8441insCATATCACC (p.Glu2814delinsAlaTyrHisGln)
13g.32371005A>CCA387752749BRCA2c.8537A>C (p.Glu2846Ala)
c.8168A>C (p.Glu2723Ala)
c.1004A>C (p.Glu335Ala)
c.8545A>C (n.8545A>C)
c.1102A>C
c.35A>C (p.Glu12Ala)
c.8441A>C (p.Glu2814Ala)
13g.32371005A>GCA387752750BRCA2c.8537A>G (p.Glu2846Gly)
c.8168A>G (p.Glu2723Gly)
c.1004A>G (p.Glu335Gly)
c.8545A>G (n.8545A>G)
c.1102A>G
c.35A>G (p.Glu12Gly)
c.8441A>G (p.Glu2814Gly)
 dbSNP
13g.32371005A>TCA387752751BRCA2c.8537A>T (p.Glu2846Val)
c.8168A>T (p.Glu2723Val)
c.1004A>T (p.Glu335Val)
c.8545A>T (n.8545A>T)
c.1102A>T
c.35A>T (p.Glu12Val)
c.8441A>T (p.Glu2814Val)

Number of alleles fetched