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.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)
13g.32371006G>ACA483261514BRCA2c.8538G>A (p.Glu2846=)
c.8169G>A (p.Glu2723=)
c.1005G>A (p.Glu335=)
c.8546G>A (n.8546G>A)
c.1103G>A
c.36G>A (p.Glu12=)
c.8442G>A (p.Glu2814=)
 ClinVar dbSNP gnomAD v4
13g.32371006G>CCA387752752BRCA2c.8538G>C (p.Glu2846Asp)
c.8169G>C (p.Glu2723Asp)
c.1005G>C (p.Glu335Asp)
c.8546G>C (n.8546G>C)
c.1103G>C
c.36G>C (p.Glu12Asp)
c.8442G>C (p.Glu2814Asp)
13g.32371006G=CA2082815658BRCA2c.8538G= (p.Glu2846=)
c.8169G= (p.Glu2723=)
c.1005G= (p.Glu335=)
c.8546G= (n.8546G=)
c.1103G=
c.36G= (p.Glu12=)
c.8442G= (p.Glu2814=)
13g.32371006G>TCA387752753BRCA2c.8538G>T (p.Glu2846Asp)
c.8169G>T (p.Glu2723Asp)
c.1005G>T (p.Glu335Asp)
c.8546G>T (n.8546G>T)
c.1103G>T
c.36G>T (p.Glu12Asp)
c.8442G>T (p.Glu2814Asp)
 dbSNP
13g.32371007G>ACA025700BRCA2c.8539G>A (p.Glu2847Lys)
c.8170G>A (p.Glu2724Lys)
c.1006G>A (p.Glu336Lys)
c.8547G>A (n.8547G>A)
c.1104G>A
c.37G>A (p.Glu13Lys)
c.8443G>A (p.Glu2815Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32371007G>CCA387752754BRCA2c.8539G>C (p.Glu2847Gln)
c.8170G>C (p.Glu2724Gln)
c.1006G>C (p.Glu336Gln)
c.8547G>C (n.8547G>C)
c.1104G>C
c.37G>C (p.Glu13Gln)
c.8443G>C (p.Glu2815Gln)
 dbSNP
13g.32371007G=CA2082815669BRCA2c.8539G= (p.Glu2847=)
c.8170G= (p.Glu2724=)
c.1006G= (p.Glu336=)
c.8547G= (n.8547G=)
c.1104G=
c.37G= (p.Glu13=)
c.8443G= (p.Glu2815=)
13g.32371007G>TCA387752755BRCA2c.8539G>T (p.Glu2847Ter)
c.8170G>T (p.Glu2724Ter)
c.1006G>T (p.Glu336Ter)
c.8547G>T (n.8547G>T)
c.1104G>T
c.37G>T (p.Glu13Ter)
c.8443G>T (p.Glu2815Ter)
13g.32371008A>CCA387752756BRCA2c.8540A>C (p.Glu2847Ala)
c.8171A>C (p.Glu2724Ala)
c.1007A>C (p.Glu336Ala)
c.8548A>C (n.8548A>C)
c.1105A>C
c.38A>C (p.Glu13Ala)
c.8444A>C (p.Glu2815Ala)
 ClinVar
13g.32371008A>GCA387752757BRCA2c.8540A>G (p.Glu2847Gly)
c.8171A>G (p.Glu2724Gly)
c.1007A>G (p.Glu336Gly)
c.8548A>G (n.8548A>G)
c.1105A>G
c.38A>G (p.Glu13Gly)
c.8444A>G (p.Glu2815Gly)
13g.32371008A>TCA387752758BRCA2c.8540A>T (p.Glu2847Val)
c.8171A>T (p.Glu2724Val)
c.1007A>T (p.Glu336Val)
c.8548A>T (n.8548A>T)
c.1105A>T
c.38A>T (p.Glu13Val)
c.8444A>T (p.Glu2815Val)
13g.32371009delCA1139770838BRCA2c.8541del (p.Glu2848LysfsTer15)
c.8172del (p.Glu2725LysfsTer15)
c.1008del (p.Glu337LysfsTer15)
c.8549del (n.8549del)
c.1106del
c.39del (p.Glu14LysfsTer15)
c.8445del (p.Glu2816LysfsTer15)
13g.32371009A=CA2082815674BRCA2c.8541A= (p.Glu2847=)
c.8172A= (p.Glu2724=)
c.1008A= (p.Glu336=)
c.8549A= (n.8549A=)
c.1106A=
c.39A= (p.Glu13=)
c.8445A= (p.Glu2815=)
13g.32371009A>CCA387752759BRCA2c.8541A>C (p.Glu2847Asp)
c.8172A>C (p.Glu2724Asp)
c.1008A>C (p.Glu336Asp)
c.8549A>C (n.8549A>C)
c.1106A>C
c.39A>C (p.Glu13Asp)
c.8445A>C (p.Glu2815Asp)
 ClinVar dbSNP gnomAD v4
13g.32371009A>GCA483261515BRCA2c.8541A>G (p.Glu2847=)
c.8172A>G (p.Glu2724=)
c.1008A>G (p.Glu336=)
c.8549A>G (n.8549A>G)
c.1106A>G
c.39A>G (p.Glu13=)
c.8445A>G (p.Glu2815=)
13g.32371009A>TCA387752760BRCA2c.8541A>T (p.Glu2847Asp)
c.8172A>T (p.Glu2724Asp)
c.1008A>T (p.Glu336Asp)
c.8549A>T (n.8549A>T)
c.1106A>T
c.39A>T (p.Glu13Asp)
c.8445A>T (p.Glu2815Asp)
13g.32371009_32371010insTTTCA2523754506BRCA2c.8541_8542insTTT (p.Glu2847_Glu2848insPhe)
c.8172_8173insTTT (p.Glu2724_Glu2725insPhe)
c.1008_1009insTTT (p.Glu336_Glu337insPhe)
c.8549_8550insTTT (n.8549_8550insTTT)
c.1106_1107insTTT
c.39_40insTTT (p.Glu13_Glu14insPhe)
c.8445_8446insTTT (p.Glu2815_Glu2816insPhe)
13g.32371010G>ACA387752761BRCA2c.8542G>A (p.Glu2848Lys)
c.8173G>A (p.Glu2725Lys)
c.1009G>A (p.Glu337Lys)
c.8550G>A (n.8550G>A)
c.1107G>A
c.40G>A (p.Glu14Lys)
c.8446G>A (p.Glu2816Lys)
13g.32371010G>CCA025701BRCA2c.8542G>C (p.Glu2848Gln)
c.8173G>C (p.Glu2725Gln)
c.1009G>C (p.Glu337Gln)
c.8550G>C (n.8550G>C)
c.1107G>C
c.40G>C (p.Glu14Gln)
c.8446G>C (p.Glu2816Gln)
 ClinVar dbSNP
13g.32371010G=CA2082815682BRCA2c.8542G= (p.Glu2848=)
c.8173G= (p.Glu2725=)
c.1009G= (p.Glu337=)
c.8550G= (n.8550G=)
c.1107G=
c.40G= (p.Glu14=)
c.8446G= (p.Glu2816=)
13g.32371010G>TCA387752762BRCA2c.8542G>T (p.Glu2848Ter)
c.8173G>T (p.Glu2725Ter)
c.1009G>T (p.Glu337Ter)
c.8550G>T (n.8550G>T)
c.1107G>T
c.40G>T (p.Glu14Ter)
c.8446G>T (p.Glu2816Ter)
13g.32371010_32371011delinsGACA2082815681BRCA2c.8542_8543delinsGA (p.Glu2848=)
c.8173_8174delinsGA (p.Glu2725=)
c.1009_1010delinsGA (p.Glu337=)
c.8550_8551delinsGA (n.8550_8551delinsGA)
c.1107_1108delinsGA
c.40_41delinsGA (p.Glu14=)
c.8446_8447delinsGA (p.Glu2816=)
13g.32371011A>CCA387752764BRCA2c.8543A>C (p.Glu2848Ala)
c.8174A>C (p.Glu2725Ala)
c.1010A>C (p.Glu337Ala)
c.8551A>C (n.8551A>C)
c.1108A>C
c.41A>C (p.Glu14Ala)
c.8447A>C (p.Glu2816Ala)
13g.32371011A>GCA387752765BRCA2c.8543A>G (p.Glu2848Gly)
c.8174A>G (p.Glu2725Gly)
c.1010A>G (p.Glu337Gly)
c.8551A>G (n.8551A>G)
c.1108A>G
c.41A>G (p.Glu14Gly)
c.8447A>G (p.Glu2816Gly)
13g.32371011A>TCA387752763BRCA2c.8543A>T (p.Glu2848Val)
c.8174A>T (p.Glu2725Val)
c.1010A>T (p.Glu337Val)
c.8551A>T (n.8551A>T)
c.1108A>T
c.41A>T (p.Glu14Val)
c.8447A>T (p.Glu2816Val)
 dbSNP
13g.32371014delCA025704BRCA2c.8546del (p.Lys2849ArgfsTer14)
c.8177del (p.Lys2726ArgfsTer14)
c.1013del (p.Lys338ArgfsTer14)
c.8554del (n.8554del)
c.1111del
c.44del (p.Lys15ArgfsTer14)
c.8450del (p.Lys2817ArgfsTer14)
 ClinVar dbSNP
13g.32371013_32371014delCA2499222336BRCA2c.8545_8546del (p.Lys2849GlyfsTer19)
c.8176_8177del (p.Lys2726GlyfsTer19)
c.1012_1013del (p.Lys338GlyfsTer19)
c.8553_8554del (n.8553_8554del)
c.1110_1111del
c.43_44del (p.Lys15GlyfsTer19)
c.8449_8450del (p.Lys2817GlyfsTer19)
 ClinVar
13g.32371011_32371012insCGAATTCA2543985276BRCA2c.8543_8544insCGAATT (p.Glu2848delinsAspGluLeu)
c.8174_8175insCGAATT (p.Glu2725delinsAspGluLeu)
c.1010_1011insCGAATT (p.Glu337delinsAspGluLeu)
c.8551_8552insCGAATT (n.8551_8552insCGAATT)
c.1108_1109insCGAATT
c.41_42insCGAATT (p.Glu14delinsAspGluLeu)
c.8447_8448insCGAATT (p.Glu2816delinsAspGluLeu)
13g.32371012A=CA2082815693BRCA2c.8544A= (p.Glu2848=)
c.8175A= (p.Glu2725=)
c.1011A= (p.Glu337=)
c.8552A= (n.8552A=)
c.1109A=
c.42A= (p.Glu14=)
c.8448A= (p.Glu2816=)
13g.32371012A>CCA16614373BRCA2c.8544A>C (p.Glu2848Asp)
c.8175A>C (p.Glu2725Asp)
c.1011A>C (p.Glu337Asp)
c.8552A>C (n.8552A>C)
c.1109A>C
c.42A>C (p.Glu14Asp)
c.8448A>C (p.Glu2816Asp)
 ClinVar dbSNP
13g.32371012A>GCA483261516BRCA2c.8544A>G (p.Glu2848=)
c.8175A>G (p.Glu2725=)
c.1011A>G (p.Glu337=)
c.8552A>G (n.8552A>G)
c.1109A>G
c.42A>G (p.Glu14=)
c.8448A>G (p.Glu2816=)
 dbSNP
13g.32371012A>TCA025702BRCA2c.8544A>T (p.Glu2848Asp)
c.8175A>T (p.Glu2725Asp)
c.1011A>T (p.Glu337Asp)
c.8552A>T (n.8552A>T)
c.1109A>T
c.42A>T (p.Glu14Asp)
c.8448A>T (p.Glu2816Asp)
 ClinVar dbSNP
13g.32371012_32371016delinsAAAGGCA2082815699BRCA2c.8544_8548delinsAAAGG (p.Glu2848=)
c.8175_8179delinsAAAGG (p.Glu2725=)
c.1011_1015delinsAAAGG (p.Glu337=)
c.8552_8556delinsAAAGG (n.8552_8556delinsAAAGG)
c.1109_1113delinsAAAGG
c.42_46delinsAAAGG (p.Glu14=)
c.8448_8452delinsAAAGG (p.Glu2816=)
13g.32371013A=CA2082815713BRCA2c.8545A= (p.Lys2849=)
c.8176A= (p.Lys2726=)
c.1012A= (p.Lys338=)
c.8553A= (n.8553A=)
c.1110A=
c.43A= (p.Lys15=)
c.8449A= (p.Lys2817=)
13g.32371013A>CCA387752766BRCA2c.8545A>C (p.Lys2849Gln)
c.8176A>C (p.Lys2726Gln)
c.1012A>C (p.Lys338Gln)
c.8553A>C (n.8553A>C)
c.1110A>C
c.43A>C (p.Lys15Gln)
c.8449A>C (p.Lys2817Gln)
 ClinVar dbSNP
13g.32371013A>GCA025703BRCA2c.8545A>G (p.Lys2849Glu)
c.8176A>G (p.Lys2726Glu)
c.1012A>G (p.Lys338Glu)
c.8553A>G (n.8553A>G)
c.1110A>G
c.43A>G (p.Lys15Glu)
c.8449A>G (p.Lys2817Glu)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32371013A>TCA387752767BRCA2c.8545A>T (p.Lys2849Ter)
c.8176A>T (p.Lys2726Ter)
c.1012A>T (p.Lys338Ter)
c.8553A>T (n.8553A>T)
c.1110A>T
c.43A>T (p.Lys15Ter)
c.8449A>T (p.Lys2817Ter)
13g.32371016_32371019delCA025705BRCA2c.8548_8551del (p.Glu2850GlnfsTer12)
c.8179_8182del (p.Glu2727GlnfsTer12)
c.1015_1018del (p.Glu339GlnfsTer12)
c.8556_8559del (n.8556_8559del)
c.1113_1116del
c.46_49del (p.Glu16GlnfsTer12)
c.8452_8455del (p.Glu2818GlnfsTer12)
 ClinVar dbSNP
13g.32371014A>CCA387752768BRCA2c.8546A>C (p.Lys2849Thr)
c.8177A>C (p.Lys2726Thr)
c.1013A>C (p.Lys338Thr)
c.8554A>C (n.8554A>C)
c.1111A>C
c.44A>C (p.Lys15Thr)
c.8450A>C (p.Lys2817Thr)
 ClinVar
13g.32371014A>GCA387752769BRCA2c.8546A>G (p.Lys2849Arg)
c.8177A>G (p.Lys2726Arg)
c.1013A>G (p.Lys338Arg)
c.8554A>G (n.8554A>G)
c.1111A>G
c.44A>G (p.Lys15Arg)
c.8450A>G (p.Lys2817Arg)
 dbSNP
13g.32371014A>TCA387752770BRCA2c.8546A>T (p.Lys2849Met)
c.8177A>T (p.Lys2726Met)
c.1013A>T (p.Lys338Met)
c.8554A>T (n.8554A>T)
c.1111A>T
c.44A>T (p.Lys15Met)
c.8450A>T (p.Lys2817Met)
 dbSNP
13g.32371014_32371015delinsAGCA2082815721BRCA2c.8546_8547delinsAG (p.Lys2849=)
c.8177_8178delinsAG (p.Lys2726=)
c.1013_1014delinsAG (p.Lys338=)
c.8554_8555delinsAG (n.8554_8555delinsAG)
c.1111_1112delinsAG
c.44_45delinsAG (p.Lys15=)
c.8450_8451delinsAG (p.Lys2817=)
13g.32371015G>ACA6941258BRCA2c.8547G>A (p.Lys2849=)
c.8178G>A (p.Lys2726=)
c.1014G>A (p.Lys338=)
c.8555G>A (n.8555G>A)
c.1112G>A
c.45G>A (p.Lys15=)
c.8451G>A (p.Lys2817=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32371015G>CCA387752772BRCA2c.8547G>C (p.Lys2849Asn)
c.8178G>C (p.Lys2726Asn)
c.1014G>C (p.Lys338Asn)
c.8555G>C (n.8555G>C)
c.1112G>C
c.45G>C (p.Lys15Asn)
c.8451G>C (p.Lys2817Asn)
 ClinVar dbSNP
13g.32371015G=CA2082815728BRCA2c.8547G= (p.Lys2849=)
c.8178G= (p.Lys2726=)
c.1014G= (p.Lys338=)
c.8555G= (n.8555G=)
c.1112G=
c.45G= (p.Lys15=)
c.8451G= (p.Lys2817=)
13g.32371015G>TCA387752771BRCA2c.8547G>T (p.Lys2849Asn)
c.8178G>T (p.Lys2726Asn)
c.1014G>T (p.Lys338Asn)
c.8555G>T (n.8555G>T)
c.1112G>T
c.45G>T (p.Lys15Asn)
c.8451G>T (p.Lys2817Asn)
 dbSNP
13g.32371016delCA658683836BRCA2c.8548del (p.Glu2850LysfsTer13)
c.8179del (p.Glu2727LysfsTer13)
c.1015del (p.Glu339LysfsTer13)
c.8556del (n.8556del)
c.1113del
c.46del (p.Glu16LysfsTer13)
c.8452del (p.Glu2818LysfsTer13)
 ClinVar dbSNP
13g.32371016G>ACA025707BRCA2c.8548G>A (p.Glu2850Lys)
c.8179G>A (p.Glu2727Lys)
c.1015G>A (p.Glu339Lys)
c.8556G>A (n.8556G>A)
c.1113G>A
c.46G>A (p.Glu16Lys)
c.8452G>A (p.Glu2818Lys)
 ClinVar dbSNP
13g.32371016G>CCA387752773BRCA2c.8548G>C (p.Glu2850Gln)
c.8179G>C (p.Glu2727Gln)
c.1015G>C (p.Glu339Gln)
c.8556G>C (n.8556G>C)
c.1113G>C
c.46G>C (p.Glu16Gln)
c.8452G>C (p.Glu2818Gln)
 dbSNP
13g.32371016G=CA2082815741BRCA2c.8548G= (p.Glu2850=)
c.8179G= (p.Glu2727=)
c.1015G= (p.Glu339=)
c.8556G= (n.8556G=)
c.1113G=
c.46G= (p.Glu16=)
c.8452G= (p.Glu2818=)
13g.32371016G>TCA387752774BRCA2c.8548G>T (p.Glu2850Ter)
c.8179G>T (p.Glu2727Ter)
c.1015G>T (p.Glu339Ter)
c.8556G>T (n.8556G>T)
c.1113G>T
c.46G>T (p.Glu16Ter)
c.8452G>T (p.Glu2818Ter)
 ClinVar dbSNP
13g.32371016_32371017insCGTCGCCA2533674555BRCA2c.8548_8549insCGTCGC (p.Glu2850delinsAlaSerGln)
c.8179_8180insCGTCGC (p.Glu2727delinsAlaSerGln)
c.1015_1016insCGTCGC (p.Glu339delinsAlaSerGln)
c.8556_8557insCGTCGC (n.8556_8557insCGTCGC)
c.1113_1114insCGTCGC
c.46_47insCGTCGC (p.Glu16delinsAlaSerGln)
c.8452_8453insCGTCGC (p.Glu2818delinsAlaSerGln)
13g.32371017A>CCA387752775BRCA2c.8549A>C (p.Glu2850Ala)
c.8180A>C (p.Glu2727Ala)
c.1016A>C (p.Glu339Ala)
c.8557A>C (n.8557A>C)
c.1114A>C
c.47A>C (p.Glu16Ala)
c.8453A>C (p.Glu2818Ala)
13g.32371017A>GCA387752776BRCA2c.8549A>G (p.Glu2850Gly)
c.8180A>G (p.Glu2727Gly)
c.1016A>G (p.Glu339Gly)
c.8557A>G (n.8557A>G)
c.1114A>G
c.47A>G (p.Glu16Gly)
c.8453A>G (p.Glu2818Gly)
13g.32371017A>TCA387752777BRCA2c.8549A>T (p.Glu2850Val)
c.8180A>T (p.Glu2727Val)
c.1016A>T (p.Glu339Val)
c.8557A>T (n.8557A>T)
c.1114A>T
c.47A>T (p.Glu16Val)
c.8453A>T (p.Glu2818Val)
13g.32371018delCA1164681425BRCA2c.8550del (p.Ala2851GlnfsTer12)
c.8181del (p.Ala2728GlnfsTer12)
c.1017del (p.Ala340GlnfsTer12)
c.8558del (n.8558del)
c.1115del
c.48del (p.Ala17GlnfsTer12)
c.8454del (p.Ala2819GlnfsTer12)
 ClinVar dbSNP
13g.32371018A=CA2082815754BRCA2c.8550A= (p.Glu2850=)
c.8181A= (p.Glu2727=)
c.1017A= (p.Glu339=)
c.8558A= (n.8558A=)
c.1115A=
c.48A= (p.Glu16=)
c.8454A= (p.Glu2818=)
13g.32371018A>CCA387752778BRCA2c.8550A>C (p.Glu2850Asp)
c.8181A>C (p.Glu2727Asp)
c.1017A>C (p.Glu339Asp)
c.8558A>C (n.8558A>C)
c.1115A>C
c.48A>C (p.Glu16Asp)
c.8454A>C (p.Glu2818Asp)
 ClinVar dbSNP
13g.32371018A>GCA483261517BRCA2c.8550A>G (p.Glu2850=)
c.8181A>G (p.Glu2727=)
c.1017A>G (p.Glu339=)
c.8558A>G (n.8558A>G)
c.1115A>G
c.48A>G (p.Glu16=)
c.8454A>G (p.Glu2818=)
 ClinVar dbSNP
13g.32371018A>TCA387752779BRCA2c.8550A>T (p.Glu2850Asp)
c.8181A>T (p.Glu2727Asp)
c.1017A>T (p.Glu339Asp)
c.8558A>T (n.8558A>T)
c.1115A>T
c.48A>T (p.Glu16Asp)
c.8454A>T (p.Glu2818Asp)
 ClinVar dbSNP
13g.32371019G>ACA387752781BRCA2c.8551G>A (p.Ala2851Thr)
c.8182G>A (p.Ala2728Thr)
c.1018G>A (p.Ala340Thr)
c.8559G>A (n.8559G>A)
c.1116G>A
c.49G>A (p.Ala17Thr)
c.8455G>A (p.Ala2819Thr)
 dbSNP gnomAD v4
13g.32371019G>CCA387752780BRCA2c.8551G>C (p.Ala2851Pro)
c.8182G>C (p.Ala2728Pro)
c.1018G>C (p.Ala340Pro)
c.8559G>C (n.8559G>C)
c.1116G>C
c.49G>C (p.Ala17Pro)
c.8455G>C (p.Ala2819Pro)
 dbSNP
13g.32371019G=CA2082815764BRCA2c.8551G= (p.Ala2851=)
c.8182G= (p.Ala2728=)
c.1018G= (p.Ala340=)
c.8559G= (n.8559G=)
c.1116G=
c.49G= (p.Ala17=)
c.8455G= (p.Ala2819=)
13g.32371019G>TCA10579793BRCA2c.8551G>T (p.Ala2851Ser)
c.8182G>T (p.Ala2728Ser)
c.1018G>T (p.Ala340Ser)
c.8559G>T (n.8559G>T)
c.1116G>T
c.49G>T (p.Ala17Ser)
c.8455G>T (p.Ala2819Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32371019_32371038dupCA2499222337BRCA2c.8551_8570dup (p.Lys2860AsnfsTer10)
c.8182_8201dup (p.Lys2737AsnfsTer10)
c.1018_1037dup (p.Lys349AsnfsTer10)
c.8559_8578dup (n.8559_8578dup)
c.1116_1135dup
c.49_68dup (p.Lys26AsnfsTer10)
c.8455_8474dup (p.Lys2828AsnfsTer10)
13g.32371020delCA2532981625BRCA2c.8552del (p.Ala2851GlufsTer12)
c.8183del (p.Ala2728GlufsTer12)
c.1019del (p.Ala340GlufsTer12)
c.8560del (n.8560del)
c.1117del
c.50del (p.Ala17GlufsTer12)
c.8456del (p.Ala2819GlufsTer12)
13g.32371020C>ACA387752782BRCA2c.8552C>A (p.Ala2851Glu)
c.8183C>A (p.Ala2728Glu)
c.1019C>A (p.Ala340Glu)
c.8560C>A (n.8560C>A)
c.1117C>A
c.50C>A (p.Ala17Glu)
c.8456C>A (p.Ala2819Glu)
 dbSNP
13g.32371020C=CA2082815779BRCA2c.8552C= (p.Ala2851=)
c.8183C= (p.Ala2728=)
c.1019C= (p.Ala340=)
c.8560C= (n.8560C=)
c.1117C=
c.50C= (p.Ala17=)
c.8456C= (p.Ala2819=)
13g.32371020C>GCA387752783BRCA2c.8552C>G (p.Ala2851Gly)
c.8183C>G (p.Ala2728Gly)
c.1019C>G (p.Ala340Gly)
c.8560C>G (n.8560C>G)
c.1117C>G
c.50C>G (p.Ala17Gly)
c.8456C>G (p.Ala2819Gly)
 ClinVar dbSNP
13g.32371020C>TCA10579794BRCA2c.8552C>T (p.Ala2851Val)
c.8183C>T (p.Ala2728Val)
c.1019C>T (p.Ala340Val)
c.8560C>T (n.8560C>T)
c.1117C>T
c.50C>T (p.Ala17Val)
c.8456C>T (p.Ala2819Val)
 ClinVar dbSNP
13g.32371021A=CA2082815783BRCA2c.8553A= (p.Ala2851=)
c.8184A= (p.Ala2728=)
c.1020A= (p.Ala340=)
c.8561A= (n.8561A=)
c.1118A=
c.51A= (p.Ala17=)
c.8457A= (p.Ala2819=)
13g.32371021A>CCA483261518BRCA2c.8553A>C (p.Ala2851=)
c.8184A>C (p.Ala2728=)
c.1020A>C (p.Ala340=)
c.8561A>C (n.8561A>C)
c.1118A>C
c.51A>C (p.Ala17=)
c.8457A>C (p.Ala2819=)
13g.32371021A>GCA247484182BRCA2c.8553A>G (p.Ala2851=)
c.8184A>G (p.Ala2728=)
c.1020A>G (p.Ala340=)
c.8561A>G (n.8561A>G)
c.1118A>G
c.51A>G (p.Ala17=)
c.8457A>G (p.Ala2819=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32371021A>TCA483261519BRCA2c.8553A>T (p.Ala2851=)
c.8184A>T (p.Ala2728=)
c.1020A>T (p.Ala340=)
c.8561A>T (n.8561A>T)
c.1118A>T
c.51A>T (p.Ala17=)
c.8457A>T (p.Ala2819=)
 dbSNP
13g.32371022G>ACA387752784BRCA2c.8554G>A (p.Ala2852Thr)
c.8185G>A (p.Ala2729Thr)
c.1021G>A (p.Ala341Thr)
c.8562G>A (n.8562G>A)
c.1119G>A
c.52G>A (p.Ala18Thr)
c.8458G>A (p.Ala2820Thr)
 ClinVar dbSNP
13g.32371022G>CCA387752785BRCA2c.8554G>C (p.Ala2852Pro)
c.8185G>C (p.Ala2729Pro)
c.1021G>C (p.Ala341Pro)
c.8562G>C (n.8562G>C)
c.1119G>C
c.52G>C (p.Ala18Pro)
c.8458G>C (p.Ala2820Pro)
 ClinVar dbSNP gnomAD v4
13g.32371022G=CA2082815790BRCA2c.8554G= (p.Ala2852=)
c.8185G= (p.Ala2729=)
c.1021G= (p.Ala341=)
c.8562G= (n.8562G=)
c.1119G=
c.52G= (p.Ala18=)
c.8458G= (p.Ala2820=)
13g.32371022G>TCA387752786BRCA2c.8554G>T (p.Ala2852Ser)
c.8185G>T (p.Ala2729Ser)
c.1021G>T (p.Ala341Ser)
c.8562G>T (n.8562G>T)
c.1119G>T
c.52G>T (p.Ala18Ser)
c.8458G>T (p.Ala2820Ser)
13g.32371023C>ACA387752787BRCA2c.8555C>A (p.Ala2852Glu)
c.8186C>A (p.Ala2729Glu)
c.1022C>A (p.Ala341Glu)
c.8563C>A (n.8563C>A)
c.1120C>A
c.53C>A (p.Ala18Glu)
c.8459C>A (p.Ala2820Glu)
 dbSNP
13g.32371023C>GCA387752788BRCA2c.8555C>G (p.Ala2852Gly)
c.8186C>G (p.Ala2729Gly)
c.1022C>G (p.Ala341Gly)
c.8563C>G (n.8563C>G)
c.1120C>G
c.53C>G (p.Ala18Gly)
c.8459C>G (p.Ala2820Gly)
13g.32371023C>TCA387752789BRCA2c.8555C>T (p.Ala2852Val)
c.8186C>T (p.Ala2729Val)
c.1022C>T (p.Ala341Val)
c.8563C>T (n.8563C>T)
c.1120C>T
c.53C>T (p.Ala18Val)
c.8459C>T (p.Ala2820Val)
13g.32371023_32371024delinsCACA2082815800BRCA2c.8555_8556delinsCA (p.Ala2852=)
c.8186_8187delinsCA (p.Ala2729=)
c.1022_1023delinsCA (p.Ala341=)
c.8563_8564delinsCA (n.8563_8564delinsCA)
c.1120_1121delinsCA
c.53_54delinsCA (p.Ala18=)
c.8459_8460delinsCA (p.Ala2820=)
13g.32371024A=CA2082815807BRCA2c.8556A= (p.Ala2852=)
c.8187A= (p.Ala2729=)
c.1023A= (p.Ala341=)
c.8564A= (n.8564A=)
c.1121A=
c.54A= (p.Ala18=)
c.8460A= (p.Ala2820=)
13g.32371024A>CCA483261520BRCA2c.8556A>C (p.Ala2852=)
c.8187A>C (p.Ala2729=)
c.1023A>C (p.Ala341=)
c.8564A>C (n.8564A>C)
c.1121A>C
c.54A>C (p.Ala18=)
c.8460A>C (p.Ala2820=)
13g.32371024A>GCA483261521BRCA2c.8556A>G (p.Ala2852=)
c.8187A>G (p.Ala2729=)
c.1023A>G (p.Ala341=)
c.8564A>G (n.8564A>G)
c.1121A>G
c.54A>G (p.Ala18=)
c.8460A>G (p.Ala2820=)
 ClinVar dbSNP
13g.32371024A>TCA483261522BRCA2c.8556A>T (p.Ala2852=)
c.8187A>T (p.Ala2729=)
c.1023A>T (p.Ala341=)
c.8564A>T (n.8564A>T)
c.1121A>T
c.54A>T (p.Ala18=)
c.8460A>T (p.Ala2820=)
13g.32371027delCA916080527BRCA2c.8559del (p.Lys2853AsnfsTer10)
c.8190del (p.Lys2730AsnfsTer10)
c.1026del (p.Lys342AsnfsTer10)
c.8567del (n.8567del)
c.1124del
c.57del (p.Lys19AsnfsTer10)
c.8463del (p.Lys2821AsnfsTer10)
 ClinVar dbSNP
13g.32371025A=CA2082815814BRCA2c.8557A= (p.Lys2853=)
c.8188A= (p.Lys2730=)
c.1024A= (p.Lys342=)
c.8565A= (n.8565A=)
c.1122A=
c.55A= (p.Lys19=)
c.8461A= (p.Lys2821=)
13g.32371025A>CCA387752790BRCA2c.8557A>C (p.Lys2853Gln)
c.8188A>C (p.Lys2730Gln)
c.1024A>C (p.Lys342Gln)
c.8565A>C (n.8565A>C)
c.1122A>C
c.55A>C (p.Lys19Gln)
c.8461A>C (p.Lys2821Gln)
13g.32371025A>GCA387752791BRCA2c.8557A>G (p.Lys2853Glu)
c.8188A>G (p.Lys2730Glu)
c.1024A>G (p.Lys342Glu)
c.8565A>G (n.8565A>G)
c.1122A>G
c.55A>G (p.Lys19Glu)
c.8461A>G (p.Lys2821Glu)
 ClinVar
13g.32371025A>TCA16042861BRCA2c.8557A>T (p.Lys2853Ter)
c.8188A>T (p.Lys2730Ter)
c.1024A>T (p.Lys342Ter)
c.8565A>T (n.8565A>T)
c.1122A>T
c.55A>T (p.Lys19Ter)
c.8461A>T (p.Lys2821Ter)
 ClinVar dbSNP
13g.32371025_32371026insCTCA2557883067BRCA2c.8557_8558insCT (p.Lys2853ThrfsTer11)
c.8188_8189insCT (p.Lys2730ThrfsTer11)
c.1024_1025insCT (p.Lys342ThrfsTer11)
c.8565_8566insCT (n.8565_8566insCT)
c.1122_1123insCT
c.55_56insCT (p.Lys19ThrfsTer11)
c.8461_8462insCT (p.Lys2821ThrfsTer11)
13g.32371026A=CA2082815822BRCA2c.8558A= (p.Lys2853=)
c.8189A= (p.Lys2730=)
c.1025A= (p.Lys342=)
c.8566A= (n.8566A=)
c.1123A=
c.56A= (p.Lys19=)
c.8462A= (p.Lys2821=)
13g.32371026A>CCA387752792BRCA2c.8558A>C (p.Lys2853Thr)
c.8189A>C (p.Lys2730Thr)
c.1025A>C (p.Lys342Thr)
c.8566A>C (n.8566A>C)
c.1123A>C
c.56A>C (p.Lys19Thr)
c.8462A>C (p.Lys2821Thr)
13g.32371026A>GCA6941259BRCA2c.8558A>G (p.Lys2853Arg)
c.8189A>G (p.Lys2730Arg)
c.1025A>G (p.Lys342Arg)
c.8566A>G (n.8566A>G)
c.1123A>G
c.56A>G (p.Lys19Arg)
c.8462A>G (p.Lys2821Arg)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32371026A>TCA387752793BRCA2c.8558A>T (p.Lys2853Ile)
c.8189A>T (p.Lys2730Ile)
c.1025A>T (p.Lys342Ile)
c.8566A>T (n.8566A>T)
c.1123A>T
c.56A>T (p.Lys19Ile)
c.8462A>T (p.Lys2821Ile)
13g.32371026_32371030delCA2571937896BRCA2c.8558_8562del (p.Lys2853SerfsTer14)
c.8189_8193del (p.Lys2730SerfsTer14)
c.1025_1029del (p.Lys342SerfsTer14)
c.8566_8570del (n.8566_8570del)
c.1123_1127del
c.56_60del (p.Lys19SerfsTer14)
c.8462_8466del (p.Lys2821SerfsTer14)
13g.32371027A=CA2082815831BRCA2c.8559A= (p.Lys2853=)
c.8190A= (p.Lys2730=)
c.1026A= (p.Lys342=)
c.8567A= (n.8567A=)
c.1124A=
c.57A= (p.Lys19=)
c.8463A= (p.Lys2821=)
13g.32371027A>CCA387752794BRCA2c.8559A>C (p.Lys2853Asn)
c.8190A>C (p.Lys2730Asn)
c.1026A>C (p.Lys342Asn)
c.8567A>C (n.8567A>C)
c.1124A>C
c.57A>C (p.Lys19Asn)
c.8463A>C (p.Lys2821Asn)
 ClinVar
13g.32371027A>GCA16607496BRCA2c.8559A>G (p.Lys2853=)
c.8190A>G (p.Lys2730=)
c.1026A>G (p.Lys342=)
c.8567A>G (n.8567A>G)
c.1124A>G
c.57A>G (p.Lys19=)
c.8463A>G (p.Lys2821=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32371027A>TCA387752795BRCA2c.8559A>T (p.Lys2853Asn)
c.8190A>T (p.Lys2730Asn)
c.1026A>T (p.Lys342Asn)
c.8567A>T (n.8567A>T)
c.1124A>T
c.57A>T (p.Lys19Asn)
c.8463A>T (p.Lys2821Asn)
13g.32371027_32371028delinsATCA2082815829BRCA2c.8559_8560delinsAT (p.Lys2853=)
c.8190_8191delinsAT (p.Lys2730=)
c.1026_1027delinsAT (p.Lys342=)
c.8567_8568delinsAT (n.8567_8568delinsAT)
c.1124_1125delinsAT
c.57_58delinsAT (p.Lys19=)
c.8463_8464delinsAT (p.Lys2821=)
13g.32371028delCA025708BRCA2c.8560del (p.Tyr2854MetfsTer9)
c.8191del (p.Tyr2731MetfsTer9)
c.1027del (p.Tyr343MetfsTer9)
c.8568del (n.8568del)
c.1125del
c.58del (p.Tyr20MetfsTer9)
c.8464del (p.Tyr2822MetfsTer9)
 ClinVar dbSNP
13g.32371028T>ACA387752796BRCA2c.8560T>A (p.Tyr2854Asn)
c.8191T>A (p.Tyr2731Asn)
c.1027T>A (p.Tyr343Asn)
c.8568T>A (n.8568T>A)
c.1125T>A
c.58T>A (p.Tyr20Asn)
c.8464T>A (p.Tyr2822Asn)
 dbSNP
13g.32371028T>CCA387752797BRCA2c.8560T>C (p.Tyr2854His)
c.8191T>C (p.Tyr2731His)
c.1027T>C (p.Tyr343His)
c.8568T>C (n.8568T>C)
c.1125T>C
c.58T>C (p.Tyr20His)
c.8464T>C (p.Tyr2822His)
 ClinVar dbSNP
13g.32371028T>GCA387752798BRCA2c.8560T>G (p.Tyr2854Asp)
c.8191T>G (p.Tyr2731Asp)
c.1027T>G (p.Tyr343Asp)
c.8568T>G (n.8568T>G)
c.1125T>G
c.58T>G (p.Tyr20Asp)
c.8464T>G (p.Tyr2822Asp)
13g.32371028T=CA2082815837BRCA2c.8560T= (p.Tyr2854=)
c.8191T= (p.Tyr2731=)
c.1027T= (p.Tyr343=)
c.8568T= (n.8568T=)
c.1125T=
c.58T= (p.Tyr20=)
c.8464T= (p.Tyr2822=)
13g.32371028_32371029insTTCA2536171156BRCA2c.8560_8561insTT (p.Tyr2854PhefsTer10)
c.8191_8192insTT (p.Tyr2731PhefsTer10)
c.1027_1028insTT (p.Tyr343PhefsTer10)
c.8568_8569insTT (n.8568_8569insTT)
c.1125_1126insTT
c.58_59insTT (p.Tyr20PhefsTer10)
c.8464_8465insTT (p.Tyr2822PhefsTer10)
13g.32371029A>CCA387752799BRCA2c.8561A>C (p.Tyr2854Ser)
c.8192A>C (p.Tyr2731Ser)
c.1028A>C (p.Tyr343Ser)
c.8569A>C (n.8569A>C)
c.1126A>C
c.59A>C (p.Tyr20Ser)
c.8465A>C (p.Tyr2822Ser)
13g.32371029A>GCA387752800BRCA2c.8561A>G (p.Tyr2854Cys)
c.8192A>G (p.Tyr2731Cys)
c.1028A>G (p.Tyr343Cys)
c.8569A>G (n.8569A>G)
c.1126A>G
c.59A>G (p.Tyr20Cys)
c.8465A>G (p.Tyr2822Cys)
13g.32371029A>TCA387752801BRCA2c.8561A>T (p.Tyr2854Phe)
c.8192A>T (p.Tyr2731Phe)
c.1028A>T (p.Tyr343Phe)
c.8569A>T (n.8569A>T)
c.1126A>T
c.59A>T (p.Tyr20Phe)
c.8465A>T (p.Tyr2822Phe)
13g.32371029dupCA025709BRCA2c.8561dup (p.Tyr2854Ter)
c.8192dup (p.Tyr2731Ter)
c.1028dup (p.Tyr343Ter)
c.8569dup (n.8569dup)
c.1126dup
c.59dup (p.Tyr20Ter)
c.8465dup (p.Tyr2822Ter)
 ClinVar dbSNP
13g.32371029_32371030delinsATCA2082815859BRCA2c.8561_8562delinsAT (p.Tyr2854=)
c.8192_8193delinsAT (p.Tyr2731=)
c.1028_1029delinsAT (p.Tyr343=)
c.8569_8570delinsAT (n.8569_8570delinsAT)
c.1126_1127delinsAT
c.59_60delinsAT (p.Tyr20=)
c.8465_8466delinsAT (p.Tyr2822=)
13g.32371029_32371036dupCA916080528BRCA2c.8561_8568dup (p.Ala2857MetfsTer9)
c.8192_8199dup (p.Ala2734MetfsTer9)
c.1028_1035dup (p.Ala346MetfsTer9)
c.8569_8576dup (n.8569_8576dup)
c.1126_1133dup
c.59_66dup (p.Ala23MetfsTer9)
c.8465_8472dup (p.Ala2825MetfsTer9)
 ClinVar dbSNP
13g.32371029_32371030insCCTCGTCCTTCTCA2541660433BRCA2c.8561_8562insCCTCGTCCTTCT (p.Tyr2854_Val2855insLeuValLeuLeu)
c.8192_8193insCCTCGTCCTTCT (p.Tyr2731_Val2732insLeuValLeuLeu)
c.1028_1029insCCTCGTCCTTCT (p.Tyr343_Val344insLeuValLeuLeu)
c.8569_8570insCCTCGTCCTTCT (n.8569_8570insCCTCGTCCTTCT)
c.1126_1127insCCTCGTCCTTCT
c.59_60insCCTCGTCCTTCT (p.Tyr20_Val21insLeuValLeuLeu)
c.8465_8466insCCTCGTCCTTCT (p.Tyr2822_Val2823insLeuValLeuLeu)
13g.32371030delCA10589507BRCA2c.8562del (p.Tyr2854Ter)
c.8193del (p.Tyr2731Ter)
c.1029del (p.Tyr343Ter)
c.8570del (n.8570del)
c.1127del
c.60del (p.Tyr20Ter)
c.8466del (p.Tyr2822Ter)
 ClinVar dbSNP
13g.32371030T>ACA387752802BRCA2c.8562T>A (p.Tyr2854Ter)
c.8193T>A (p.Tyr2731Ter)
c.1029T>A (p.Tyr343Ter)
c.8570T>A (n.8570T>A)
c.1127T>A
c.60T>A (p.Tyr20Ter)
c.8466T>A (p.Tyr2822Ter)
 ClinVar dbSNP
13g.32371030T>CCA025710BRCA2c.8562T>C (p.Tyr2854=)
c.8193T>C (p.Tyr2731=)
c.1029T>C (p.Tyr343=)
c.8570T>C (n.8570T>C)
c.1127T>C
c.60T>C (p.Tyr20=)
c.8466T>C (p.Tyr2822=)
 ClinVar dbSNP
13g.32371030T>GCA387752803BRCA2c.8562T>G (p.Tyr2854Ter)
c.8193T>G (p.Tyr2731Ter)
c.1029T>G (p.Tyr343Ter)
c.8570T>G (n.8570T>G)
c.1127T>G
c.60T>G (p.Tyr20Ter)
c.8466T>G (p.Tyr2822Ter)
 ClinVar dbSNP
13g.32371030T=CA2082815882BRCA2c.8562T= (p.Tyr2854=)
c.8193T= (p.Tyr2731=)
c.1029T= (p.Tyr343=)
c.8570T= (n.8570T=)
c.1127T=
c.60T= (p.Tyr20=)
c.8466T= (p.Tyr2822=)
13g.32371031G>ACA387752805BRCA2c.8563G>A (p.Val2855Met)
c.8194G>A (p.Val2732Met)
c.1030G>A (p.Val344Met)
c.8571G>A (n.8571G>A)
c.1128G>A
c.61G>A (p.Val21Met)
c.8467G>A (p.Val2823Met)
 dbSNP
13g.32371031G>CCA387752806BRCA2c.8563G>C (p.Val2855Leu)
c.8194G>C (p.Val2732Leu)
c.1030G>C (p.Val344Leu)
c.8571G>C (n.8571G>C)
c.1128G>C
c.61G>C (p.Val21Leu)
c.8467G>C (p.Val2823Leu)
 dbSNP
13g.32371031G>TCA387752804BRCA2c.8563G>T (p.Val2855Leu)
c.8194G>T (p.Val2732Leu)
c.1030G>T (p.Val344Leu)
c.8571G>T (n.8571G>T)
c.1128G>T
c.61G>T (p.Val21Leu)
c.8467G>T (p.Val2823Leu)
13g.32371032T>ACA387752807BRCA2c.8564T>A (p.Val2855Glu)
c.8195T>A (p.Val2732Glu)
c.1031T>A (p.Val344Glu)
c.8572T>A (n.8572T>A)
c.1129T>A
c.62T>A (p.Val21Glu)
c.8468T>A (p.Val2823Glu)
13g.32371032T>CCA387752808BRCA2c.8564T>C (p.Val2855Ala)
c.8195T>C (p.Val2732Ala)
c.1031T>C (p.Val344Ala)
c.8572T>C (n.8572T>C)
c.1129T>C
c.62T>C (p.Val21Ala)
c.8468T>C (p.Val2823Ala)
13g.32371032T>GCA387752809BRCA2c.8564T>G (p.Val2855Gly)
c.8195T>G (p.Val2732Gly)
c.1031T>G (p.Val344Gly)
c.8572T>G (n.8572T>G)
c.1129T>G
c.62T>G (p.Val21Gly)
c.8468T>G (p.Val2823Gly)
13g.32371032_32371033delinsTGCA2082815971BRCA2c.8564_8565delinsTG (p.Val2855=)
c.8195_8196delinsTG (p.Val2732=)
c.1031_1032delinsTG (p.Val344=)
c.8572_8573delinsTG (n.8572_8573delinsTG)
c.1129_1130delinsTG
c.62_63delinsTG (p.Val21=)
c.8468_8469delinsTG (p.Val2823=)
13g.32371033G>ACA025711BRCA2c.8565G>A (p.Val2855=)
c.8196G>A (p.Val2732=)
c.1032G>A (p.Val344=)
c.8573G>A (n.8573G>A)
c.1130G>A
c.63G>A (p.Val21=)
c.8469G>A (p.Val2823=)
 ClinVar dbSNP
13g.32371033G>CCA10579795BRCA2c.8565G>C (p.Val2855=)
c.8196G>C (p.Val2732=)
c.1032G>C (p.Val344=)
c.8573G>C (n.8573G>C)
c.1130G>C
c.63G>C (p.Val21=)
c.8469G>C (p.Val2823=)
 ClinVar dbSNP
13g.32371033G=CA2082815992BRCA2c.8565G= (p.Val2855=)
c.8196G= (p.Val2732=)
c.1032G= (p.Val344=)
c.8573G= (n.8573G=)
c.1130G=
c.63G= (p.Val21=)
c.8469G= (p.Val2823=)
13g.32371033G>TCA483261523BRCA2c.8565G>T (p.Val2855=)
c.8196G>T (p.Val2732=)
c.1032G>T (p.Val344=)
c.8573G>T (n.8573G>T)
c.1130G>T
c.63G>T (p.Val21=)
c.8469G>T (p.Val2823=)
13g.32371034delCA10589508BRCA2c.8566del (p.Glu2856ArgfsTer7)
c.8197del (p.Glu2733ArgfsTer7)
c.1033del (p.Glu345ArgfsTer7)
c.8574del (n.8574del)
c.1131del
c.64del (p.Glu22ArgfsTer7)
c.8470del (p.Glu2824ArgfsTer7)
 ClinVar dbSNP
13g.32371033_32371035delinsGGACA2082815999BRCA2c.8565_8567delinsGGA (p.Val2855=)
c.8196_8198delinsGGA (p.Val2732=)
c.1032_1034delinsGGA (p.Val344=)
c.8573_8575delinsGGA (n.8573_8575delinsGGA)
c.1130_1132delinsGGA
c.63_65delinsGGA (p.Val21=)
c.8469_8471delinsGGA (p.Val2823=)
13g.32371033_32371034insTCCA2519823764BRCA2c.8565_8566insTC (p.Glu2856SerfsTer8)
c.8196_8197insTC (p.Glu2733SerfsTer8)
c.1032_1033insTC (p.Glu345SerfsTer8)
c.8573_8574insTC (n.8573_8574insTC)
c.1130_1131insTC
c.63_64insTC (p.Glu22SerfsTer8)
c.8469_8470insTC (p.Glu2824SerfsTer8)
13g.32371034G>ACA387752810BRCA2c.8566G>A (p.Glu2856Lys)
c.8197G>A (p.Glu2733Lys)
c.1033G>A (p.Glu345Lys)
c.8574G>A (n.8574G>A)
c.1131G>A
c.64G>A (p.Glu22Lys)
c.8470G>A (p.Glu2824Lys)
 dbSNP
13g.32371034G>CCA387752811BRCA2c.8566G>C (p.Glu2856Gln)
c.8197G>C (p.Glu2733Gln)
c.1033G>C (p.Glu345Gln)
c.8574G>C (n.8574G>C)
c.1131G>C
c.64G>C (p.Glu22Gln)
c.8470G>C (p.Glu2824Gln)
 dbSNP
13g.32371034G>TCA387752812BRCA2c.8566G>T (p.Glu2856Ter)
c.8197G>T (p.Glu2733Ter)
c.1033G>T (p.Glu345Ter)
c.8574G>T (n.8574G>T)
c.1131G>T
c.64G>T (p.Glu22Ter)
c.8470G>T (p.Glu2824Ter)
13g.32371034_32371035delinsCCA10576074BRCA2c.8566_8567delinsC (p.Glu2856ArgfsTer7)
c.8197_8198delinsC (p.Glu2733ArgfsTer7)
c.1033_1034delinsC (p.Glu345ArgfsTer7)
c.8574_8575delinsC (n.8574_8575delinsC)
c.1131_1132delinsC
c.64_65delinsC (p.Glu22ArgfsTer7)
c.8470_8471delinsC (p.Glu2824ArgfsTer7)
 ClinVar dbSNP
13g.32371034_32371039delCA2515000285BRCA2c.8566_8571del (p.Glu2856_Ala2857del)
c.8197_8202del (p.Glu2733_Ala2734del)
c.1033_1038del (p.Glu345_Ala346del)
c.8574_8579del (n.8574_8579del)
c.1131_1136del
c.64_69del (p.Glu22_Ala23del)
c.8470_8475del (p.Glu2824_Ala2825del)
13g.32371035A=CA2082816016BRCA2c.8567A= (p.Glu2856=)
c.8198A= (p.Glu2733=)
c.1034A= (p.Glu345=)
c.8575A= (n.8575A=)
c.1132A=
c.65A= (p.Glu22=)
c.8471A= (p.Glu2824=)
13g.32371035A>CCA025712BRCA2c.8567A>C (p.Glu2856Ala)
c.8198A>C (p.Glu2733Ala)
c.1034A>C (p.Glu345Ala)
c.8575A>C (n.8575A>C)
c.1132A>C
c.65A>C (p.Glu22Ala)
c.8471A>C (p.Glu2824Ala)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32371035A>GCA387752813BRCA2c.8567A>G (p.Glu2856Gly)
c.8198A>G (p.Glu2733Gly)
c.1034A>G (p.Glu345Gly)
c.8575A>G (n.8575A>G)
c.1132A>G
c.65A>G (p.Glu22Gly)
c.8471A>G (p.Glu2824Gly)
 dbSNP
13g.32371035A>TCA387752814BRCA2c.8567A>T (p.Glu2856Val)
c.8198A>T (p.Glu2733Val)
c.1034A>T (p.Glu345Val)
c.8575A>T (n.8575A>T)
c.1132A>T
c.65A>T (p.Glu22Val)
c.8471A>T (p.Glu2824Val)
 ClinVar dbSNP
13g.32371036G>ACA16606451BRCA2c.8568G>A (p.Glu2856=)
c.8199G>A (p.Glu2733=)
c.1035G>A (p.Glu345=)
c.8576G>A (n.8576G>A)
c.1133G>A
c.66G>A (p.Glu22=)
c.8472G>A (p.Glu2824=)
 ClinVar dbSNP
13g.32371036G>CCA387752815BRCA2c.8568G>C (p.Glu2856Asp)
c.8199G>C (p.Glu2733Asp)
c.1035G>C (p.Glu345Asp)
c.8576G>C (n.8576G>C)
c.1133G>C
c.66G>C (p.Glu22Asp)
c.8472G>C (p.Glu2824Asp)
 ClinVar dbSNP
13g.32371036G=CA2082816025BRCA2c.8568G= (p.Glu2856=)
c.8199G= (p.Glu2733=)
c.1035G= (p.Glu345=)
c.8576G= (n.8576G=)
c.1133G=
c.66G= (p.Glu22=)
c.8472G= (p.Glu2824=)
13g.32371036G>TCA10583143BRCA2c.8568G>T (p.Glu2856Asp)
c.8199G>T (p.Glu2733Asp)
c.1035G>T (p.Glu345Asp)
c.8576G>T (n.8576G>T)
c.1133G>T
c.66G>T (p.Glu22Asp)
c.8472G>T (p.Glu2824Asp)
 ClinVar dbSNP
13g.32371037delCA2573149215BRCA2c.8569del (p.Ala2857ProfsTer6)
c.8200del (p.Ala2734ProfsTer6)
c.1036del (p.Ala346ProfsTer6)
c.8577del (n.8577del)
c.1134del
c.67del (p.Ala23ProfsTer6)
c.8473del (p.Ala2825ProfsTer6)
 ClinVar dbSNP
13g.32371037G>ACA387752816BRCA2c.8569G>A (p.Ala2857Thr)
c.8200G>A (p.Ala2734Thr)
c.1036G>A (p.Ala346Thr)
c.8577G>A (n.8577G>A)
c.1134G>A
c.67G>A (p.Ala23Thr)
c.8473G>A (p.Ala2825Thr)
 ClinVar dbSNP
13g.32371037G>CCA350121BRCA2c.8569G>C (p.Ala2857Pro)
c.8200G>C (p.Ala2734Pro)
c.1036G>C (p.Ala346Pro)
c.8577G>C (n.8577G>C)
c.1134G>C
c.67G>C (p.Ala23Pro)
c.8473G>C (p.Ala2825Pro)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32371037G=CA2082816045BRCA2c.8569G= (p.Ala2857=)
c.8200G= (p.Ala2734=)
c.1036G= (p.Ala346=)
c.8577G= (n.8577G=)
c.1134G=
c.67G= (p.Ala23=)
c.8473G= (p.Ala2825=)
13g.32371037G>TCA025713BRCA2c.8569G>T (p.Ala2857Ser)
c.8200G>T (p.Ala2734Ser)
c.1036G>T (p.Ala346Ser)
c.8577G>T (n.8577G>T)
c.1134G>T
c.67G>T (p.Ala23Ser)
c.8473G>T (p.Ala2825Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32371037_32371038delinsGCCA2082816053BRCA2c.8569_8570delinsGC (p.Ala2857=)
c.8200_8201delinsGC (p.Ala2734=)
c.1036_1037delinsGC (p.Ala346=)
c.8577_8578delinsGC (n.8577_8578delinsGC)
c.1134_1135delinsGC
c.67_68delinsGC (p.Ala23=)
c.8473_8474delinsGC (p.Ala2825=)
13g.32371037_32371044delCA2511483729BRCA2c.8569_8576del (p.Ala2857LysfsTer9)
c.8200_8207del (p.Ala2734LysfsTer9)
c.1036_1043del (p.Ala346LysfsTer9)
c.8577_8584del (n.8577_8584del)
c.1134_1141del
c.67_74del (p.Ala23LysfsTer9)
c.8473_8480del (p.Ala2825LysfsTer9)
13g.32371038C>ACA387752817BRCA2c.8570C>A (p.Ala2857Asp)
c.8201C>A (p.Ala2734Asp)
c.1037C>A (p.Ala346Asp)
c.8578C>A (n.8578C>A)
c.1135C>A
c.68C>A (p.Ala23Asp)
c.8474C>A (p.Ala2825Asp)
 dbSNP
13g.32371038C=CA2082816065BRCA2c.8570C= (p.Ala2857=)
c.8201C= (p.Ala2734=)
c.1037C= (p.Ala346=)
c.8578C= (n.8578C=)
c.1135C=
c.68C= (p.Ala23=)
c.8474C= (p.Ala2825=)
13g.32371038C>GCA387752818BRCA2c.8570C>G (p.Ala2857Gly)
c.8201C>G (p.Ala2734Gly)
c.1037C>G (p.Ala346Gly)
c.8578C>G (n.8578C>G)
c.1135C>G
c.68C>G (p.Ala23Gly)
c.8474C>G (p.Ala2825Gly)
 dbSNP
13g.32371038C>TCA6941260BRCA2c.8570C>T (p.Ala2857Val)
c.8201C>T (p.Ala2734Val)
c.1037C>T (p.Ala346Val)
c.8578C>T (n.8578C>T)
c.1135C>T
c.68C>T (p.Ala23Val)
c.8474C>T (p.Ala2825Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32371040delCA10589509BRCA2c.8572del (p.Gln2858AsnfsTer5)
c.8203del (p.Gln2735AsnfsTer5)
c.1039del (p.Gln347AsnfsTer5)
c.8580del (n.8580del)
c.1137del
c.70del (p.Gln24AsnfsTer5)
c.8476del (p.Gln2826AsnfsTer5)
 ClinVar dbSNP
13g.32371039C>ACA483261524BRCA2c.8571C>A (p.Ala2857=)
c.8202C>A (p.Ala2734=)
c.1038C>A (p.Ala346=)
c.8579C>A (n.8579C>A)
c.1136C>A
c.69C>A (p.Ala23=)
c.8475C>A (p.Ala2825=)
 ClinVar dbSNP
13g.32371039C>GCA483261525BRCA2c.8571C>G (p.Ala2857=)
c.8202C>G (p.Ala2734=)
c.1038C>G (p.Ala346=)
c.8579C>G (n.8579C>G)
c.1136C>G
c.69C>G (p.Ala23=)
c.8475C>G (p.Ala2825=)
 dbSNP
13g.32371039C>TCA483261526BRCA2c.8571C>T (p.Ala2857=)
c.8202C>T (p.Ala2734=)
c.1038C>T (p.Ala346=)
c.8579C>T (n.8579C>T)
c.1136C>T
c.69C>T (p.Ala23=)
c.8475C>T (p.Ala2825=)
 ClinVar dbSNP gnomAD v4
13g.32371040C>ACA025715BRCA2c.8572C>A (p.Gln2858Lys)
c.8203C>A (p.Gln2735Lys)
c.1039C>A (p.Gln347Lys)
c.8580C>A (n.8580C>A)
c.1137C>A
c.70C>A (p.Gln24Lys)
c.8476C>A (p.Gln2826Lys)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32371040C=CA2082816082BRCA2c.8572C= (p.Gln2858=)
c.8203C= (p.Gln2735=)
c.1039C= (p.Gln347=)
c.8580C= (n.8580C=)
c.1137C=
c.70C= (p.Gln24=)
c.8476C= (p.Gln2826=)
13g.32371040C>GCA387752819BRCA2c.8572C>G (p.Gln2858Glu)
c.8203C>G (p.Gln2735Glu)
c.1039C>G (p.Gln347Glu)
c.8580C>G (n.8580C>G)
c.1137C>G
c.70C>G (p.Gln24Glu)
c.8476C>G (p.Gln2826Glu)
13g.32371040C>TCA025716BRCA2c.8572C>T (p.Gln2858Ter)
c.8203C>T (p.Gln2735Ter)
c.1039C>T (p.Gln347Ter)
c.8580C>T (n.8580C>T)
c.1137C>T
c.70C>T (p.Gln24Ter)
c.8476C>T (p.Gln2826Ter)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32371041A=CA2082816095BRCA2c.8573A= (p.Gln2858=)
c.8204A= (p.Gln2735=)
c.1040A= (p.Gln347=)
c.8581A= (n.8581A=)
c.1138A=
c.71A= (p.Gln24=)
c.8477A= (p.Gln2826=)
13g.32371041A>CCA387752820BRCA2c.8573A>C (p.Gln2858Pro)
c.8204A>C (p.Gln2735Pro)
c.1040A>C (p.Gln347Pro)
c.8581A>C (n.8581A>C)
c.1138A>C
c.71A>C (p.Gln24Pro)
c.8477A>C (p.Gln2826Pro)
 ClinVar dbSNP
13g.32371041A>GCA025717BRCA2c.8573A>G (p.Gln2858Arg)
c.8204A>G (p.Gln2735Arg)
c.1040A>G (p.Gln347Arg)
c.8581A>G (n.8581A>G)
c.1138A>G
c.71A>G (p.Gln24Arg)
c.8477A>G (p.Gln2826Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32371041A>TCA387752821BRCA2c.8573A>T (p.Gln2858Leu)
c.8204A>T (p.Gln2735Leu)
c.1040A>T (p.Gln347Leu)
c.8581A>T (n.8581A>T)
c.1138A>T
c.71A>T (p.Gln24Leu)
c.8477A>T (p.Gln2826Leu)
 dbSNP
13g.32371042A=CA2082816116BRCA2c.8574A= (p.Gln2858=)
c.8205A= (p.Gln2735=)
c.1041A= (p.Gln347=)
c.8582A= (n.8582A=)
c.1139A=
c.72A= (p.Gln24=)
c.8478A= (p.Gln2826=)
13g.32371042A>CCA387752822BRCA2c.8574A>C (p.Gln2858His)
c.8205A>C (p.Gln2735His)
c.1041A>C (p.Gln347His)
c.8582A>C (n.8582A>C)
c.1139A>C
c.72A>C (p.Gln24His)
c.8478A>C (p.Gln2826His)
 dbSNP
13g.32371042A>GCA483261527BRCA2c.8574A>G (p.Gln2858=)
c.8205A>G (p.Gln2735=)
c.1041A>G (p.Gln347=)
c.8582A>G (n.8582A>G)
c.1139A>G
c.72A>G (p.Gln24=)
c.8478A>G (p.Gln2826=)
 dbSNP
13g.32371042A>TCA387752823BRCA2c.8574A>T (p.Gln2858His)
c.8205A>T (p.Gln2735His)
c.1041A>T (p.Gln347His)
c.8582A>T (n.8582A>T)
c.1139A>T
c.72A>T (p.Gln24His)
c.8478A>T (p.Gln2826His)
 dbSNP
13g.32371042_32371043delinsACCA2082816114BRCA2c.8574_8575delinsAC (p.Gln2858=)
c.8205_8206delinsAC (p.Gln2735=)
c.1041_1042delinsAC (p.Gln347=)
c.8582_8583delinsAC (n.8582_8583delinsAC)
c.1139_1140delinsAC
c.72_73delinsAC (p.Gln24=)
c.8478_8479delinsAC (p.Gln2826=)
13g.32371043delCA025719BRCA2c.8575del (p.Gln2859LysfsTer4)
c.8206del (p.Gln2736LysfsTer4)
c.1042del (p.Gln348LysfsTer4)
c.8583del (n.8583del)
c.1140del
c.73del (p.Gln25LysfsTer4)
c.8479del (p.Gln2827LysfsTer4)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32371043C>ACA387752824BRCA2c.8575C>A (p.Gln2859Lys)
c.8206C>A (p.Gln2736Lys)
c.1042C>A (p.Gln348Lys)
c.8583C>A (n.8583C>A)
c.1140C>A
c.73C>A (p.Gln25Lys)
c.8479C>A (p.Gln2827Lys)
 ClinVar dbSNP gnomAD v4
13g.32371043C=CA2082816129BRCA2c.8575C= (p.Gln2859=)
c.8206C= (p.Gln2736=)
c.1042C= (p.Gln348=)
c.8583C= (n.8583C=)
c.1140C=
c.73C= (p.Gln25=)
c.8479C= (p.Gln2827=)
13g.32371043C>GCA387752825BRCA2c.8575C>G (p.Gln2859Glu)
c.8206C>G (p.Gln2736Glu)
c.1042C>G (p.Gln348Glu)
c.8583C>G (n.8583C>G)
c.1140C>G
c.73C>G (p.Gln25Glu)
c.8479C>G (p.Gln2827Glu)
13g.32371043C>TCA025718BRCA2c.8575C>T (p.Gln2859Ter)
c.8206C>T (p.Gln2736Ter)
c.1042C>T (p.Gln348Ter)
c.8583C>T (n.8583C>T)
c.1140C>T
c.73C>T (p.Gln25Ter)
c.8479C>T (p.Gln2827Ter)
 ClinVar dbSNP
13g.32371043dupCA2798730082BRCA2c.8575dup (p.Gln2859ProfsTer10)
c.8206dup (p.Gln2736ProfsTer10)
c.1042dup (p.Gln348ProfsTer10)
c.8583dup (n.8583dup)
c.1140dup
c.73dup (p.Gln25ProfsTer10)
c.8479dup (p.Gln2827ProfsTer10)
13g.32371043_32371045delinsCAACA2082816134BRCA2c.8575_8577delinsCAA (p.Gln2859=)
c.8206_8208delinsCAA (p.Gln2736=)
c.1042_1044delinsCAA (p.Gln348=)
c.8583_8585delinsCAA (n.8583_8585delinsCAA)
c.1140_1142delinsCAA
c.73_75delinsCAA (p.Gln25=)
c.8479_8481delinsCAA (p.Gln2827=)
13g.32371044A>CCA387752827BRCA2c.8576A>C (p.Gln2859Pro)
c.8207A>C (p.Gln2736Pro)
c.1043A>C (p.Gln348Pro)
c.8584A>C (n.8584A>C)
c.1141A>C
c.74A>C (p.Gln25Pro)
c.8480A>C (p.Gln2827Pro)
 ClinVar dbSNP
13g.32371044A>GCA387752826BRCA2c.8576A>G (p.Gln2859Arg)
c.8207A>G (p.Gln2736Arg)
c.1043A>G (p.Gln348Arg)
c.8584A>G (n.8584A>G)
c.1141A>G
c.74A>G (p.Gln25Arg)
c.8480A>G (p.Gln2827Arg)
 ClinVar dbSNP
13g.32371044A>TCA387752828BRCA2c.8576A>T (p.Gln2859Leu)
c.8207A>T (p.Gln2736Leu)
c.1043A>T (p.Gln348Leu)
c.8584A>T (n.8584A>T)
c.1141A>T
c.74A>T (p.Gln25Leu)
c.8480A>T (p.Gln2827Leu)
13g.32371047delCA025721BRCA2c.8579del (p.Lys2860ArgfsTer3)
c.8210del (p.Lys2737ArgfsTer3)
c.1046del (p.Lys349ArgfsTer3)
c.8587del (n.8587del)
c.1144del
c.77del (p.Lys26ArgfsTer3)
c.8483del (p.Lys2828ArgfsTer3)
 ClinVar dbSNP
13g.32371046_32371047delCA025720BRCA2c.8578_8579del (p.Lys2860GlufsTer8)
c.8209_8210del (p.Lys2737GlufsTer8)
c.1045_1046del (p.Lys349GlufsTer8)
c.8586_8587del (n.8586_8587del)
c.1143_1144del
c.76_77del (p.Lys26GlufsTer8)
c.8482_8483del (p.Lys2828GlufsTer8)
 ClinVar dbSNP
13g.32371045A>CCA387752830BRCA2c.8577A>C (p.Gln2859His)
c.8208A>C (p.Gln2736His)
c.1044A>C (p.Gln348His)
c.8585A>C (n.8585A>C)
c.1142A>C
c.75A>C (p.Gln25His)
c.8481A>C (p.Gln2827His)
 ClinVar dbSNP
13g.32371045A>GCA483261529BRCA2c.8577A>G (p.Gln2859=)
c.8208A>G (p.Gln2736=)
c.1044A>G (p.Gln348=)
c.8585A>G (n.8585A>G)
c.1142A>G
c.75A>G (p.Gln25=)
c.8481A>G (p.Gln2827=)
 ClinVar dbSNP
13g.32371045A>TCA387752829BRCA2c.8577A>T (p.Gln2859His)
c.8208A>T (p.Gln2736His)
c.1044A>T (p.Gln348His)
c.8585A>T (n.8585A>T)
c.1142A>T
c.75A>T (p.Gln25His)
c.8481A>T (p.Gln2827His)
 dbSNP
13g.32371046A>CCA387752831BRCA2c.8578A>C (p.Lys2860Gln)
c.8209A>C (p.Lys2737Gln)
c.1045A>C (p.Lys349Gln)
c.8586A>C (n.8586A>C)
c.1143A>C
c.76A>C (p.Lys26Gln)
c.8482A>C (p.Lys2828Gln)
13g.32371046A>GCA387752833BRCA2c.8578A>G (p.Lys2860Glu)
c.8209A>G (p.Lys2737Glu)
c.1045A>G (p.Lys349Glu)
c.8586A>G (n.8586A>G)
c.1143A>G
c.76A>G (p.Lys26Glu)
c.8482A>G (p.Lys2828Glu)
13g.32371046A>TCA387752832BRCA2c.8578A>T (p.Lys2860Ter)
c.8209A>T (p.Lys2737Ter)
c.1045A>T (p.Lys349Ter)
c.8586A>T (n.8586A>T)
c.1143A>T
c.76A>T (p.Lys26Ter)
c.8482A>T (p.Lys2828Ter)
13g.32371046_32371048delinsAAGCA2082816148BRCA2c.8578_8580delinsAAG (p.Lys2860=)
c.8209_8211delinsAAG (p.Lys2737=)
c.1045_1047delinsAAG (p.Lys349=)
c.8586_8588delinsAAG (n.8586_8588delinsAAG)
c.1143_1145delinsAAG
c.76_78delinsAAG (p.Lys26=)
c.8482_8484delinsAAG (p.Lys2828=)
13g.32371046_32371047insTTTCA2507872694BRCA2c.8578_8579insTTT (p.Lys2860IlefsTer2)
c.8209_8210insTTT (p.Lys2737IlefsTer2)
c.1045_1046insTTT (p.Lys349IlefsTer2)
c.8586_8587insTTT (n.8586_8587insTTT)
c.1143_1144insTTT
c.76_77insTTT (p.Lys26IlefsTer2)
c.8482_8483insTTT (p.Lys2828IlefsTer2)
13g.32371047A>CCA387752834BRCA2c.8579A>C (p.Lys2860Thr)
c.8210A>C (p.Lys2737Thr)
c.1046A>C (p.Lys349Thr)
c.8587A>C (n.8587A>C)
c.1144A>C
c.77A>C (p.Lys26Thr)
c.8483A>C (p.Lys2828Thr)
 dbSNP
13g.32371047A>GCA387752835BRCA2c.8579A>G (p.Lys2860Arg)
c.8210A>G (p.Lys2737Arg)
c.1046A>G (p.Lys349Arg)
c.8587A>G (n.8587A>G)
c.1144A>G
c.77A>G (p.Lys26Arg)
c.8483A>G (p.Lys2828Arg)
 ClinVar dbSNP gnomAD v4
13g.32371047A>TCA387752836BRCA2c.8579A>T (p.Lys2860Met)
c.8210A>T (p.Lys2737Met)
c.1046A>T (p.Lys349Met)
c.8587A>T (n.8587A>T)
c.1144A>T
c.77A>T (p.Lys26Met)
c.8483A>T (p.Lys2828Met)
13g.32371047_32371048insACCCAAACACACCCAACACACA2798730083BRCA2c.8579_8580insACCCAAACACACCCAACACA (p.Arg2861ProfsTer9)
c.8210_8211insACCCAAACACACCCAACACA (p.Arg2738ProfsTer9)
c.1046_1047insACCCAAACACACCCAACACA (p.Arg350ProfsTer9)
c.8587_8588insACCCAAACACACCCAACACA (n.8587_8588insACCCAAACACACCCAACACA)
c.1144_1145insACCCAAACACACCCAACACA
c.77_78insACCCAAACACACCCAACACA (p.Arg27ProfsTer9)
c.8483_8484insACCCAAACACACCCAACACA (p.Arg2829ProfsTer9)
13g.32371050_32371051delCA915946899BRCA2c.8582_8583del (p.Arg2861ThrfsTer7)
c.8213_8214del (p.Arg2738ThrfsTer7)
c.1049_1050del (p.Arg350ThrfsTer7)
c.8590_8591del (n.8590_8591del)
c.1147_1148del
c.80_81del (p.Arg27ThrfsTer7)
c.8486_8487del (p.Arg2829ThrfsTer7)
 ClinVar dbSNP
13g.32371047_32371048insTCCACCTCA2514116880BRCA2c.8579_8580insTCCACCT (p.Lys2860AsnfsTer11)
c.8210_8211insTCCACCT (p.Lys2737AsnfsTer11)
c.1046_1047insTCCACCT (p.Lys349AsnfsTer11)
c.8587_8588insTCCACCT (n.8587_8588insTCCACCT)
c.1144_1145insTCCACCT
c.77_78insTCCACCT (p.Lys26AsnfsTer11)
c.8483_8484insTCCACCT (p.Lys2828AsnfsTer11)
13g.32371048G>ACA483261530BRCA2c.8580G>A (p.Lys2860=)
c.8211G>A (p.Lys2737=)
c.1047G>A (p.Lys349=)
c.8588G>A (n.8588G>A)
c.1145G>A
c.78G>A (p.Lys26=)
c.8484G>A (p.Lys2828=)
 dbSNP
13g.32371048G>CCA387752837BRCA2c.8580G>C (p.Lys2860Asn)
c.8211G>C (p.Lys2737Asn)
c.1047G>C (p.Lys349Asn)
c.8588G>C (n.8588G>C)
c.1145G>C
c.78G>C (p.Lys26Asn)
c.8484G>C (p.Lys2828Asn)
 dbSNP
13g.32371048G>TCA387752838BRCA2c.8580G>T (p.Lys2860Asn)
c.8211G>T (p.Lys2737Asn)
c.1047G>T (p.Lys349Asn)
c.8588G>T (n.8588G>T)
c.1145G>T
c.78G>T (p.Lys26Asn)
c.8484G>T (p.Lys2828Asn)
13g.32371048_32371050delCA2551397038BRCA2c.8580_8582del (p.Arg2861del)
c.8211_8213del (p.Arg2738del)
c.1047_1049del (p.Arg350del)
c.8588_8590del (n.8588_8590del)
c.1145_1147del
c.78_80del (p.Arg27del)
c.8484_8486del (p.Arg2829del)
13g.32371049A=CA2082816168BRCA2c.8581A= (p.Arg2861=)
c.8212A= (p.Arg2738=)
c.1048A= (p.Arg350=)
c.8589A= (n.8589A=)
c.1146A=
c.79A= (p.Arg27=)
c.8485A= (p.Arg2829=)
13g.32371049A>CCA483261531BRCA2c.8581A>C (p.Arg2861=)
c.8212A>C (p.Arg2738=)
c.1048A>C (p.Arg350=)
c.8589A>C (n.8589A>C)
c.1146A>C
c.79A>C (p.Arg27=)
c.8485A>C (p.Arg2829=)
13g.32371049A>GCA387752839BRCA2c.8581A>G (p.Arg2861Gly)
c.8212A>G (p.Arg2738Gly)
c.1048A>G (p.Arg350Gly)
c.8589A>G (n.8589A>G)
c.1146A>G
c.79A>G (p.Arg27Gly)
c.8485A>G (p.Arg2829Gly)
 ClinVar
13g.32371049A>TCA025722BRCA2c.8581A>T (p.Arg2861Ter)
c.8212A>T (p.Arg2738Ter)
c.1048A>T (p.Arg350Ter)
c.8589A>T (n.8589A>T)
c.1146A>T
c.79A>T (p.Arg27Ter)
c.8485A>T (p.Arg2829Ter)
 ClinVar dbSNP
13g.32371050G>ACA387752840BRCA2c.8582G>A (p.Arg2861Lys)
c.8213G>A (p.Arg2738Lys)
c.1049G>A (p.Arg350Lys)
c.8590G>A (n.8590G>A)
c.1147G>A
c.80G>A (p.Arg27Lys)
c.8486G>A (p.Arg2829Lys)
 dbSNP
13g.32371050G>CCA387752841BRCA2c.8582G>C (p.Arg2861Thr)
c.8213G>C (p.Arg2738Thr)
c.1049G>C (p.Arg350Thr)
c.8590G>C (n.8590G>C)
c.1147G>C
c.80G>C (p.Arg27Thr)
c.8486G>C (p.Arg2829Thr)
 dbSNP
13g.32371050G=CA2082816178BRCA2c.8582G= (p.Arg2861=)
c.8213G= (p.Arg2738=)
c.1049G= (p.Arg350=)
c.8590G= (n.8590G=)
c.1147G=
c.80G= (p.Arg27=)
c.8486G= (p.Arg2829=)
13g.32371050G>TCA387752842BRCA2c.8582G>T (p.Arg2861Ile)
c.8213G>T (p.Arg2738Ile)
c.1049G>T (p.Arg350Ile)
c.8590G>T (n.8590G>T)
c.1147G>T
c.80G>T (p.Arg27Ile)
c.8486G>T (p.Arg2829Ile)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32371050_32371052dupCA915946900BRCA2c.8582_8584dup (p.Arg2861_Leu2862insArg)
c.8213_8215dup (p.Arg2738_Leu2739insArg)
c.1049_1051dup (p.Arg350_Leu351insArg)
c.8590_8592dup (n.8590_8592dup)
c.1147_1149dup
c.80_82dup (p.Arg27_Leu28insArg)
c.8486_8488dup (p.Arg2829_Leu2830insArg)
 ClinVar dbSNP
13g.32371051A>CCA387752843BRCA2c.8583A>C (p.Arg2861Ser)
c.8214A>C (p.Arg2738Ser)
c.1050A>C (p.Arg350Ser)
c.8591A>C (n.8591A>C)
c.1148A>C
c.81A>C (p.Arg27Ser)
c.8487A>C (p.Arg2829Ser)
13g.32371051A>GCA483261535BRCA2c.8583A>G (p.Arg2861=)
c.8214A>G (p.Arg2738=)
c.1050A>G (p.Arg350=)
c.8591A>G (n.8591A>G)
c.1148A>G
c.81A>G (p.Arg27=)
c.8487A>G (p.Arg2829=)
 ClinVar dbSNP gnomAD v4
13g.32371051A>TCA387752844BRCA2c.8583A>T (p.Arg2861Ser)
c.8214A>T (p.Arg2738Ser)
c.1050A>T (p.Arg350Ser)
c.8591A>T (n.8591A>T)
c.1148A>T
c.81A>T (p.Arg27Ser)
c.8487A>T (p.Arg2829Ser)
 dbSNP
13g.32371051_32371057delCA2536684871BRCA2c.8583_8589del (p.Leu2862ProfsTer27)
c.8583_8589del (p.Leu2862ProfsTer22)
c.8214_8220del (p.Leu2739ProfsTer27)
c.8583_8589del (p.Leu2862ProfsTer28)
c.1050_1056del (p.Leu351ProfsTer27)
c.8591_8597del (n.8591_8597del)
c.1148_1154del
c.81_87del (p.Leu28ProfsTer22)
c.8487_8493del (p.Leu2830ProfsTer27)
13g.32371052C>ACA387752845BRCA2c.8584C>A (p.Leu2862Ile)
c.8215C>A (p.Leu2739Ile)
c.1051C>A (p.Leu351Ile)
c.8592C>A (n.8592C>A)
c.1149C>A
c.82C>A (p.Leu28Ile)
c.8488C>A (p.Leu2830Ile)
 ClinVar dbSNP gnomAD v4
13g.32371052C=CA2082816187BRCA2c.8584C= (p.Leu2862=)
c.8215C= (p.Leu2739=)
c.1051C= (p.Leu351=)
c.8592C= (n.8592C=)
c.1149C=
c.82C= (p.Leu28=)
c.8488C= (p.Leu2830=)
13g.32371052C>GCA387752846BRCA2c.8584C>G (p.Leu2862Val)
c.8215C>G (p.Leu2739Val)
c.1051C>G (p.Leu351Val)
c.8592C>G (n.8592C>G)
c.1149C>G
c.82C>G (p.Leu28Val)
c.8488C>G (p.Leu2830Val)
 dbSNP
13g.32371052C>TCA483261537BRCA2c.8584C>T (p.Leu2862=)
c.8215C>T (p.Leu2739=)
c.1051C>T (p.Leu351=)
c.8592C>T (n.8592C>T)
c.1149C>T
c.82C>T (p.Leu28=)
c.8488C>T (p.Leu2830=)
 ClinVar dbSNP gnomAD v4
13g.32371052_32371054delinsCTACA2082816188BRCA2c.8584_8586delinsCTA (p.Leu2862=)
c.8215_8217delinsCTA (p.Leu2739=)
c.1051_1053delinsCTA (p.Leu351=)
c.8592_8594delinsCTA (n.8592_8594delinsCTA)
c.1149_1151delinsCTA
c.82_84delinsCTA (p.Leu28=)
c.8488_8490delinsCTA (p.Leu2830=)
13g.32371053T>ACA387752847BRCA2c.8585T>A (p.Leu2862Gln)
c.8216T>A (p.Leu2739Gln)
c.1052T>A (p.Leu351Gln)
c.8593T>A (n.8593T>A)
c.1150T>A
c.83T>A (p.Leu28Gln)
c.8489T>A (p.Leu2830Gln)
 ClinVar dbSNP
13g.32371053T>CCA387752849BRCA2c.8585T>C (p.Leu2862Pro)
c.8216T>C (p.Leu2739Pro)
c.1052T>C (p.Leu351Pro)
c.8593T>C (n.8593T>C)
c.1150T>C
c.83T>C (p.Leu28Pro)
c.8489T>C (p.Leu2830Pro)
13g.32371053T>GCA387752848BRCA2c.8585T>G (p.Leu2862Arg)
c.8216T>G (p.Leu2739Arg)
c.1052T>G (p.Leu351Arg)
c.8593T>G (n.8593T>G)
c.1150T>G
c.83T>G (p.Leu28Arg)
c.8489T>G (p.Leu2830Arg)
13g.32371053T=CA2082816206BRCA2c.8585T= (p.Leu2862=)
c.8216T= (p.Leu2739=)
c.1052T= (p.Leu351=)
c.8593T= (n.8593T=)
c.1150T=
c.83T= (p.Leu28=)
c.8489T= (p.Leu2830=)
13g.32371053dupCA025723BRCA2c.8585dup (p.Glu2863ArgfsTer6)
c.8216dup (p.Glu2740ArgfsTer6)
c.1052dup (p.Glu352ArgfsTer6)
c.8593dup (n.8593dup)
c.1150dup
c.83dup (p.Glu29ArgfsTer6)
c.8489dup (p.Glu2831ArgfsTer6)
 ClinVar dbSNP gnomAD v4
13g.32371053_32371054delCA10583144BRCA2c.8585_8586del (p.Leu2862ArgfsTer6)
c.8216_8217del (p.Leu2739ArgfsTer6)
c.1052_1053del (p.Leu351ArgfsTer6)
c.8593_8594del (n.8593_8594del)
c.1150_1151del
c.83_84del (p.Leu28ArgfsTer6)
c.8489_8490del (p.Leu2830ArgfsTer6)
 ClinVar dbSNP
13g.32371053_32371054delinsAGCA658656383BRCA2c.8585_8586delinsAG (p.Leu2862Gln)
c.8216_8217delinsAG (p.Leu2739Gln)
c.1052_1053delinsAG (p.Leu351Gln)
c.8593_8594delinsAG (n.8593_8594delinsAG)
c.1150_1151delinsAG
c.83_84delinsAG (p.Leu28Gln)
c.8489_8490delinsAG (p.Leu2830Gln)
 ClinVar dbSNP
13g.32371053_32371054delinsTACA2082816214BRCA2c.8585_8586delinsTA (p.Leu2862=)
c.8216_8217delinsTA (p.Leu2739=)
c.1052_1053delinsTA (p.Leu351=)
c.8593_8594delinsTA (n.8593_8594delinsTA)
c.1150_1151delinsTA
c.83_84delinsTA (p.Leu28=)
c.8489_8490delinsTA (p.Leu2830=)
13g.32371054A=CA2082816235BRCA2c.8586A= (p.Leu2862=)
c.8217A= (p.Leu2739=)
c.1053A= (p.Leu351=)
c.8594A= (n.8594A=)
c.1151A=
c.84A= (p.Leu28=)
c.8490A= (p.Leu2830=)
13g.32371054A>CCA483261541BRCA2c.8586A>C (p.Leu2862=)
c.8217A>C (p.Leu2739=)
c.1053A>C (p.Leu351=)
c.8594A>C (n.8594A>C)
c.1151A>C
c.84A>C (p.Leu28=)
c.8490A>C (p.Leu2830=)
13g.32371054A>GCA483261539BRCA2c.8586A>G (p.Leu2862=)
c.8217A>G (p.Leu2739=)
c.1053A>G (p.Leu351=)
c.8594A>G (n.8594A>G)
c.1151A>G
c.84A>G (p.Leu28=)
c.8490A>G (p.Leu2830=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32371054A>TCA483261543BRCA2c.8586A>T (p.Leu2862=)
c.8217A>T (p.Leu2739=)
c.1053A>T (p.Leu351=)
c.8594A>T (n.8594A>T)
c.1151A>T
c.84A>T (p.Leu28=)
c.8490A>T (p.Leu2830=)
 ClinVar dbSNP
13g.32371056_32371058dupCA025724BRCA2c.8588_8590dup (p.Glu2863_Ala2864insGlu)
c.8219_8221dup (p.Glu2740_Ala2741insGlu)
c.1055_1057dup (p.Glu352_Ala353insGlu)
c.8596_8598dup (n.8596_8598dup)
c.1153_1155dup
c.86_88dup (p.Glu29_Ala30insGlu)
c.8492_8494dup (p.Glu2831_Ala2832insGlu)
 ClinVar dbSNP gnomAD v4
13g.32371055G>ACA387752850BRCA2c.8587G>A (p.Glu2863Lys)
c.8218G>A (p.Glu2740Lys)
c.1054G>A (p.Glu352Lys)
c.8595G>A (n.8595G>A)
c.1152G>A
c.85G>A (p.Glu29Lys)
c.8491G>A (p.Glu2831Lys)
 dbSNP
13g.32371055G>CCA387752851BRCA2c.8587G>C (p.Glu2863Gln)
c.8218G>C (p.Glu2740Gln)
c.1054G>C (p.Glu352Gln)
c.8595G>C (n.8595G>C)
c.1152G>C
c.85G>C (p.Glu29Gln)
c.8491G>C (p.Glu2831Gln)
 ClinVar dbSNP
13g.32371055G=CA2082816249BRCA2c.8587G= (p.Glu2863=)
c.8218G= (p.Glu2740=)
c.1054G= (p.Glu352=)
c.8595G= (n.8595G=)
c.1152G=
c.85G= (p.Glu29=)
c.8491G= (p.Glu2831=)
13g.32371055G>TCA387752852BRCA2c.8587G>T (p.Glu2863Ter)
c.8218G>T (p.Glu2740Ter)
c.1054G>T (p.Glu352Ter)
c.8595G>T (n.8595G>T)
c.1152G>T
c.85G>T (p.Glu29Ter)
c.8491G>T (p.Glu2831Ter)
 dbSNP COSMIC COSMIC
13g.32371055dupCA2499222338BRCA2c.8587dup (p.Glu2863GlyfsTer6)
c.8218dup (p.Glu2740GlyfsTer6)
c.1054dup (p.Glu352GlyfsTer6)
c.8595dup (n.8595dup)
c.1152dup
c.85dup (p.Glu29GlyfsTer6)
c.8491dup (p.Glu2831GlyfsTer6)
 ClinVar
13g.32371056A=CA2082816259BRCA2c.8588A= (p.Glu2863=)
c.8219A= (p.Glu2740=)
c.1055A= (p.Glu352=)
c.8596A= (n.8596A=)
c.1153A=
c.86A= (p.Glu29=)
c.8492A= (p.Glu2831=)
13g.32371056A>CCA387752853BRCA2c.8588A>C (p.Glu2863Ala)
c.8219A>C (p.Glu2740Ala)
c.1055A>C (p.Glu352Ala)
c.8596A>C (n.8596A>C)
c.1153A>C
c.86A>C (p.Glu29Ala)
c.8492A>C (p.Glu2831Ala)
13g.32371056A>GCA387752854BRCA2c.8588A>G (p.Glu2863Gly)
c.8219A>G (p.Glu2740Gly)
c.1055A>G (p.Glu352Gly)
c.8596A>G (n.8596A>G)
c.1153A>G
c.86A>G (p.Glu29Gly)
c.8492A>G (p.Glu2831Gly)
13g.32371056A>TCA387752855BRCA2c.8588A>T (p.Glu2863Val)
c.8219A>T (p.Glu2740Val)
c.1055A>T (p.Glu352Val)
c.8596A>T (n.8596A>T)
c.1153A>T
c.86A>T (p.Glu29Val)
c.8492A>T (p.Glu2831Val)
 ClinVar dbSNP
13g.32371057dupCA658761177BRCA2c.8589dup (p.Ala2864SerfsTer5)
c.8220dup (p.Ala2741SerfsTer5)
c.1056dup (p.Ala353SerfsTer5)
c.8597dup (n.8597dup)
c.1154dup
c.87dup (p.Ala30SerfsTer5)
c.8493dup (p.Ala2832SerfsTer5)
 ClinVar dbSNP gnomAD v4
13g.32371057A>CCA387752856BRCA2c.8589A>C (p.Glu2863Asp)
c.8220A>C (p.Glu2740Asp)
c.1056A>C (p.Glu352Asp)
c.8597A>C (n.8597A>C)
c.1154A>C
c.87A>C (p.Glu29Asp)
c.8493A>C (p.Glu2831Asp)
13g.32371057A>GCA483261544BRCA2c.8589A>G (p.Glu2863=)
c.8220A>G (p.Glu2740=)
c.1056A>G (p.Glu352=)
c.8597A>G (n.8597A>G)
c.1154A>G
c.87A>G (p.Glu29=)
c.8493A>G (p.Glu2831=)
 ClinVar
13g.32371057A>TCA387752857BRCA2c.8589A>T (p.Glu2863Asp)
c.8220A>T (p.Glu2740Asp)
c.1056A>T (p.Glu352Asp)
c.8597A>T (n.8597A>T)
c.1154A>T
c.87A>T (p.Glu29Asp)
c.8493A>T (p.Glu2831Asp)
 dbSNP
13g.32371057_32371060delinsAGCCCA2082816266BRCA2c.8589_8592delinsAGCC (p.Glu2863=)
c.8220_8223delinsAGCC (p.Glu2740=)
c.1056_1059delinsAGCC (p.Glu352=)
c.8597_8600delinsAGCC (n.8597_8600delinsAGCC)
c.1154_1157delinsAGCC
c.87_90delinsAGCC (p.Glu29=)
c.8493_8496delinsAGCC (p.Glu2831=)
13g.32371058G>ACA387752860BRCA2c.8590G>A (p.Ala2864Thr)
c.8221G>A (p.Ala2741Thr)
c.1057G>A (p.Ala353Thr)
c.8598G>A (n.8598G>A)
c.1155G>A
c.88G>A (p.Ala30Thr)
c.8494G>A (p.Ala2832Thr)
 ClinVar dbSNP gnomAD v4
13g.32371058G>CCA387752859BRCA2c.8590G>C (p.Ala2864Pro)
c.8221G>C (p.Ala2741Pro)
c.1057G>C (p.Ala353Pro)
c.8598G>C (n.8598G>C)
c.1155G>C
c.88G>C (p.Ala30Pro)
c.8494G>C (p.Ala2832Pro)
 dbSNP
13g.32371058G=CA2082816275BRCA2c.8590G= (p.Ala2864=)
c.8221G= (p.Ala2741=)
c.1057G= (p.Ala353=)
c.8598G= (n.8598G=)
c.1155G=
c.88G= (p.Ala30=)
c.8494G= (p.Ala2832=)
13g.32371058G>TCA387752858BRCA2c.8590G>T (p.Ala2864Ser)
c.8221G>T (p.Ala2741Ser)
c.1057G>T (p.Ala353Ser)
c.8598G>T (n.8598G>T)
c.1155G>T
c.88G>T (p.Ala30Ser)
c.8494G>T (p.Ala2832Ser)
 ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC
13g.32371058_32371059delinsGCCA2082816272BRCA2c.8590_8591delinsGC (p.Ala2864=)
c.8221_8222delinsGC (p.Ala2741=)
c.1057_1058delinsGC (p.Ala353=)
c.8598_8599delinsGC (n.8598_8599delinsGC)
c.1155_1156delinsGC
c.88_89delinsGC (p.Ala30=)
c.8494_8495delinsGC (p.Ala2832=)
13g.32371058_32371060delCA658656384BRCA2c.8590_8592del (p.Ala2864del)
c.8221_8223del (p.Ala2741del)
c.1057_1059del (p.Ala353del)
c.8598_8600del (n.8598_8600del)
c.1155_1157del
c.88_90del (p.Ala30del)
c.8494_8496del (p.Ala2832del)
 ClinVar dbSNP gnomAD v4
13g.32371059C>ACA387752862BRCA2c.8591C>A (p.Ala2864Asp)
c.8222C>A (p.Ala2741Asp)
c.1058C>A (p.Ala353Asp)
c.8599C>A (n.8599C>A)
c.1156C>A
c.89C>A (p.Ala30Asp)
c.8495C>A (p.Ala2832Asp)
 ClinVar dbSNP
13g.32371059C=CA2082816289BRCA2c.8591C= (p.Ala2864=)
c.8222C= (p.Ala2741=)
c.1058C= (p.Ala353=)
c.8599C= (n.8599C=)
c.1156C=
c.89C= (p.Ala30=)
c.8495C= (p.Ala2832=)
13g.32371059C>GCA387752861BRCA2c.8591C>G (p.Ala2864Gly)
c.8222C>G (p.Ala2741Gly)
c.1058C>G (p.Ala353Gly)
c.8599C>G (n.8599C>G)
c.1156C>G
c.89C>G (p.Ala30Gly)
c.8495C>G (p.Ala2832Gly)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32371059C>TCA025725BRCA2c.8591C>T (p.Ala2864Val)
c.8222C>T (p.Ala2741Val)
c.1058C>T (p.Ala353Val)
c.8599C>T (n.8599C>T)
c.1156C>T
c.89C>T (p.Ala30Val)
c.8495C>T (p.Ala2832Val)
 ClinVar dbSNP gnomAD v4
13g.32371060delCA658823597BRCA2c.8592del (p.Leu2865TyrfsTer26)
c.8592del (p.Leu2865TyrfsTer21)
c.8223del (p.Leu2742TyrfsTer26)
c.8592del (p.Leu2865TyrfsTer27)
c.1059del (p.Leu354TyrfsTer26)
c.8600del (n.8600del)
c.1157del
c.90del (p.Leu31TyrfsTer21)
c.8496del (p.Leu2833TyrfsTer26)
 ClinVar dbSNP
13g.32371060C>ACA483261545BRCA2c.8592C>A (p.Ala2864=)
c.8223C>A (p.Ala2741=)
c.1059C>A (p.Ala353=)
c.8600C>A (n.8600C>A)
c.1157C>A
c.90C>A (p.Ala30=)
c.8496C>A (p.Ala2832=)
 dbSNP
13g.32371060C=CA2082816305BRCA2c.8592C= (p.Ala2864=)
c.8223C= (p.Ala2741=)
c.1059C= (p.Ala353=)
c.8600C= (n.8600C=)
c.1157C=
c.90C= (p.Ala30=)
c.8496C= (p.Ala2832=)
13g.32371060C>GCA483261546BRCA2c.8592C>G (p.Ala2864=)
c.8223C>G (p.Ala2741=)
c.1059C>G (p.Ala353=)
c.8600C>G (n.8600C>G)
c.1157C>G
c.90C>G (p.Ala30=)
c.8496C>G (p.Ala2832=)
 dbSNP
13g.32371060C>TCA6941261BRCA2c.8592C>T (p.Ala2864=)
c.8223C>T (p.Ala2741=)
c.1059C>T (p.Ala353=)
c.8600C>T (n.8600C>T)
c.1157C>T
c.90C>T (p.Ala30=)
c.8496C>T (p.Ala2832=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32371061T>ACA387752863BRCA2c.8593T>A (p.Leu2865Ile)
c.8224T>A (p.Leu2742Ile)
c.1060T>A (p.Leu354Ile)
c.8601T>A (n.8601T>A)
c.1158T>A
c.91T>A (p.Leu31Ile)
c.8497T>A (p.Leu2833Ile)
 ClinVar dbSNP
13g.32371061T>CCA483261548BRCA2c.8593T>C (p.Leu2865=)
c.8224T>C (p.Leu2742=)
c.1060T>C (p.Leu354=)
c.8601T>C (n.8601T>C)
c.1158T>C
c.91T>C (p.Leu31=)
c.8497T>C (p.Leu2833=)
 dbSNP gnomAD v4
13g.32371061T>GCA025727BRCA2c.8593T>G (p.Leu2865Val)
c.8224T>G (p.Leu2742Val)
c.1060T>G (p.Leu354Val)
c.8601T>G (n.8601T>G)
c.1158T>G
c.91T>G (p.Leu31Val)
c.8497T>G (p.Leu2833Val)
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC
13g.32371061T=CA2082816329BRCA2c.8593T= (p.Leu2865=)
c.8224T= (p.Leu2742=)
c.1060T= (p.Leu354=)
c.8601T= (n.8601T=)
c.1158T=
c.91T= (p.Leu31=)
c.8497T= (p.Leu2833=)
13g.32371062dupCA025726BRCA2c.8594dup (p.Leu2865PhefsTer4)
c.8225dup (p.Leu2742PhefsTer4)
c.1061dup (p.Leu354PhefsTer4)
c.8602dup (n.8602dup)
c.1159dup
c.92dup (p.Leu31PhefsTer4)
c.8498dup (p.Leu2833PhefsTer4)
 ClinVar dbSNP
13g.32371062T>ACA025729BRCA2c.8594T>A (p.Leu2865Ter)
c.8225T>A (p.Leu2742Ter)
c.1061T>A (p.Leu354Ter)
c.8602T>A (n.8602T>A)
c.1159T>A
c.92T>A (p.Leu31Ter)
c.8498T>A (p.Leu2833Ter)
 ClinVar dbSNP
13g.32371062T>CCA387752864BRCA2c.8594T>C (p.Leu2865Ser)
c.8225T>C (p.Leu2742Ser)
c.1061T>C (p.Leu354Ser)
c.8602T>C (n.8602T>C)
c.1159T>C
c.92T>C (p.Leu31Ser)
c.8498T>C (p.Leu2833Ser)
 ClinVar dbSNP
13g.32371062T>GCA387752865BRCA2c.8594T>G (p.Leu2865Ter)
c.8225T>G (p.Leu2742Ter)
c.1061T>G (p.Leu354Ter)
c.8602T>G (n.8602T>G)
c.1159T>G
c.92T>G (p.Leu31Ter)
c.8498T>G (p.Leu2833Ter)
 dbSNP
13g.32371062T=CA2082816340BRCA2c.8594T= (p.Leu2865=)
c.8225T= (p.Leu2742=)
c.1061T= (p.Leu354=)
c.8602T= (n.8602T=)
c.1159T=
c.92T= (p.Leu31=)
c.8498T= (p.Leu2833=)
13g.32371063A=CA2082816348BRCA2c.8595A= (p.Leu2865=)
c.8226A= (p.Leu2742=)
c.1062A= (p.Leu354=)
c.8603A= (n.8603A=)
c.1160A=
c.93A= (p.Leu31=)
c.8499A= (p.Leu2833=)
13g.32371063A>CCA387752866BRCA2c.8595A>C (p.Leu2865Phe)
c.8226A>C (p.Leu2742Phe)
c.1062A>C (p.Leu354Phe)
c.8603A>C (n.8603A>C)
c.1160A>C
c.93A>C (p.Leu31Phe)
c.8499A>C (p.Leu2833Phe)
13g.32371063A>GCA483261551BRCA2c.8595A>G (p.Leu2865=)
c.8226A>G (p.Leu2742=)
c.1062A>G (p.Leu354=)
c.8603A>G (n.8603A>G)
c.1160A>G
c.93A>G (p.Leu31=)
c.8499A>G (p.Leu2833=)
 ClinVar dbSNP
13g.32371063A>TCA387752867BRCA2c.8595A>T (p.Leu2865Phe)
c.8226A>T (p.Leu2742Phe)
c.1062A>T (p.Leu354Phe)
c.8603A>T (n.8603A>T)
c.1160A>T
c.93A>T (p.Leu31Phe)
c.8499A>T (p.Leu2833Phe)
 ClinVar dbSNP gnomAD v4
13g.32371064T>ACA387752868BRCA2c.8596T>A (p.Phe2866Ile)
c.8227T>A (p.Phe2743Ile)
c.1063T>A (p.Phe355Ile)
c.8604T>A (n.8604T>A)
c.1161T>A
c.94T>A (p.Phe32Ile)
c.8500T>A (p.Phe2834Ile)
 dbSNP
13g.32371064T>CCA387752869BRCA2c.8596T>C (p.Phe2866Leu)
c.8227T>C (p.Phe2743Leu)
c.1063T>C (p.Phe355Leu)
c.8604T>C (n.8604T>C)
c.1161T>C
c.94T>C (p.Phe32Leu)
c.8500T>C (p.Phe2834Leu)
 dbSNP gnomAD v4
13g.32371064T>GCA387752870BRCA2c.8596T>G (p.Phe2866Val)
c.8227T>G (p.Phe2743Val)
c.1063T>G (p.Phe355Val)
c.8604T>G (n.8604T>G)
c.1161T>G
c.94T>G (p.Phe32Val)
c.8500T>G (p.Phe2834Val)
 ClinVar dbSNP
13g.32371064T=CA2082816355BRCA2c.8596T= (p.Phe2866=)
c.8227T= (p.Phe2743=)
c.1063T= (p.Phe355=)
c.8604T= (n.8604T=)
c.1161T=
c.94T= (p.Phe32=)
c.8500T= (p.Phe2834=)
13g.32371065T>ACA387752872BRCA2c.8597T>A (p.Phe2866Tyr)
c.8228T>A (p.Phe2743Tyr)
c.1064T>A (p.Phe355Tyr)
c.8605T>A (n.8605T>A)
c.1162T>A
c.95T>A (p.Phe32Tyr)
c.8501T>A (p.Phe2834Tyr)
13g.32371065T>CCA387752875BRCA2c.8597T>C (p.Phe2866Ser)
c.8228T>C (p.Phe2743Ser)
c.1064T>C (p.Phe355Ser)
c.8605T>C (n.8605T>C)
c.1162T>C
c.95T>C (p.Phe32Ser)
c.8501T>C (p.Phe2834Ser)
13g.32371065T>GCA387752874BRCA2c.8597T>G (p.Phe2866Cys)
c.8228T>G (p.Phe2743Cys)
c.1064T>G (p.Phe355Cys)
c.8605T>G (n.8605T>G)
c.1162T>G
c.95T>G (p.Phe32Cys)
c.8501T>G (p.Phe2834Cys)
13g.32371066C>ACA387752877BRCA2c.8598C>A (p.Phe2866Leu)
c.8229C>A (p.Phe2743Leu)
c.1065C>A (p.Phe355Leu)
c.8606C>A (n.8606C>A)
c.1163C>A
c.96C>A (p.Phe32Leu)
c.8502C>A (p.Phe2834Leu)
 dbSNP
13g.32371066C>GCA387752878BRCA2c.8598C>G (p.Phe2866Leu)
c.8229C>G (p.Phe2743Leu)
c.1065C>G (p.Phe355Leu)
c.8606C>G (n.8606C>G)
c.1163C>G
c.96C>G (p.Phe32Leu)
c.8502C>G (p.Phe2834Leu)
 dbSNP
13g.32371066C>TCA483261555BRCA2c.8598C>T (p.Phe2866=)
c.8229C>T (p.Phe2743=)
c.1065C>T (p.Phe355=)
c.8606C>T (n.8606C>T)
c.1163C>T
c.96C>T (p.Phe32=)
c.8502C>T (p.Phe2834=)
 dbSNP
13g.32371067A=CA2082816361BRCA2c.8599A= (p.Thr2867=)
c.8230A= (p.Thr2744=)
c.1066A= (p.Thr356=)
c.8607A= (n.8607A=)
c.1164A=
c.97A= (p.Thr33=)
c.8503A= (p.Thr2835=)
13g.32371067A>CCA025730BRCA2c.8599A>C (p.Thr2867Pro)
c.8230A>C (p.Thr2744Pro)
c.1066A>C (p.Thr356Pro)
c.8607A>C (n.8607A>C)
c.1164A>C
c.97A>C (p.Thr33Pro)
c.8503A>C (p.Thr2835Pro)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32371067A>GCA387752880BRCA2c.8599A>G (p.Thr2867Ala)
c.8230A>G (p.Thr2744Ala)
c.1066A>G (p.Thr356Ala)
c.8607A>G (n.8607A>G)
c.1164A>G
c.97A>G (p.Thr33Ala)
c.8503A>G (p.Thr2835Ala)
 ClinVar
13g.32371067A>TCA387752881BRCA2c.8599A>T (p.Thr2867Ser)
c.8230A>T (p.Thr2744Ser)
c.1066A>T (p.Thr356Ser)
c.8607A>T (n.8607A>T)
c.1164A>T
c.97A>T (p.Thr33Ser)
c.8503A>T (p.Thr2835Ser)
 dbSNP
13g.32371068C>ACA387752884BRCA2c.8600C>A (p.Thr2867Asn)
c.8231C>A (p.Thr2744Asn)
c.1067C>A (p.Thr356Asn)
c.8608C>A (n.8608C>A)
c.1165C>A
c.98C>A (p.Thr33Asn)
c.8504C>A (p.Thr2835Asn)
13g.32371068C=CA2082816368BRCA2c.8600C= (p.Thr2867=)
c.8231C= (p.Thr2744=)
c.1067C= (p.Thr356=)
c.8608C= (n.8608C=)
c.1165C=
c.98C= (p.Thr33=)
c.8504C= (p.Thr2835=)
13g.32371068C>GCA387752886BRCA2c.8600C>G (p.Thr2867Ser)
c.8231C>G (p.Thr2744Ser)
c.1067C>G (p.Thr356Ser)
c.8608C>G (n.8608C>G)
c.1165C>G
c.98C>G (p.Thr33Ser)
c.8504C>G (p.Thr2835Ser)
 dbSNP
13g.32371068C>TCA387752887BRCA2c.8600C>T (p.Thr2867Ile)
c.8231C>T (p.Thr2744Ile)
c.1067C>T (p.Thr356Ile)
c.8608C>T (n.8608C>T)
c.1165C>T
c.98C>T (p.Thr33Ile)
c.8504C>T (p.Thr2835Ile)
 ClinVar dbSNP
13g.32371069T>ACA483261556BRCA2c.8601T>A (p.Thr2867=)
c.8232T>A (p.Thr2744=)
c.1068T>A (p.Thr356=)
c.8609T>A (n.8609T>A)
c.1166T>A
c.99T>A (p.Thr33=)
c.8505T>A (p.Thr2835=)
13g.32371069T>CCA483261557BRCA2c.8601T>C (p.Thr2867=)
c.8232T>C (p.Thr2744=)
c.1068T>C (p.Thr356=)
c.8609T>C (n.8609T>C)
c.1166T>C
c.99T>C (p.Thr33=)
c.8505T>C (p.Thr2835=)
13g.32371069T>GCA483261558BRCA2c.8601T>G (p.Thr2867=)
c.8232T>G (p.Thr2744=)
c.1068T>G (p.Thr356=)
c.8609T>G (n.8609T>G)
c.1166T>G
c.99T>G (p.Thr33=)
c.8505T>G (p.Thr2835=)
13g.32371069dupCA025731BRCA2c.8601dup (p.Lys2868Ter)
c.8232dup (p.Lys2745Ter)
c.1068dup (p.Lys357Ter)
c.8609dup (n.8609dup)
c.1166dup
c.99dup (p.Lys34Ter)
c.8505dup (p.Lys2836Ter)
 ClinVar dbSNP
13g.32371070A=CA2082816373BRCA2c.8602A= (p.Lys2868=)
c.8233A= (p.Lys2745=)
c.1069A= (p.Lys357=)
c.8610A= (n.8610A=)
c.1167A=
c.100A= (p.Lys34=)
c.8506A= (p.Lys2836=)
13g.32371070A>CCA387752890BRCA2c.8602A>C (p.Lys2868Gln)
c.8233A>C (p.Lys2745Gln)
c.1069A>C (p.Lys357Gln)
c.8610A>C (n.8610A>C)
c.1167A>C
c.100A>C (p.Lys34Gln)
c.8506A>C (p.Lys2836Gln)
13g.32371070A>GCA387752891BRCA2c.8602A>G (p.Lys2868Glu)
c.8233A>G (p.Lys2745Glu)
c.1069A>G (p.Lys357Glu)
c.8610A>G (n.8610A>G)
c.1167A>G
c.100A>G (p.Lys34Glu)
c.8506A>G (p.Lys2836Glu)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32371070A>TCA387752892BRCA2c.8602A>T (p.Lys2868Ter)
c.8233A>T (p.Lys2745Ter)
c.1069A>T (p.Lys357Ter)
c.8610A>T (n.8610A>T)
c.1167A>T
c.100A>T (p.Lys34Ter)
c.8506A>T (p.Lys2836Ter)
13g.32371071A=CA2082816381BRCA2c.8603A= (p.Lys2868=)
c.8234A= (p.Lys2745=)
c.1070A= (p.Lys357=)
c.8611A= (n.8611A=)
c.1168A=
c.101A= (p.Lys34=)
c.8507A= (p.Lys2836=)
13g.32371071A>CCA387752896BRCA2c.8603A>C (p.Lys2868Thr)
c.8234A>C (p.Lys2745Thr)
c.1070A>C (p.Lys357Thr)
c.8611A>C (n.8611A>C)
c.1168A>C
c.101A>C (p.Lys34Thr)
c.8507A>C (p.Lys2836Thr)
13g.32371071A>GCA6941262BRCA2c.8603A>G (p.Lys2868Arg)
c.8234A>G (p.Lys2745Arg)
c.1070A>G (p.Lys357Arg)
c.8611A>G (n.8611A>G)
c.1168A>G
c.101A>G (p.Lys34Arg)
c.8507A>G (p.Lys2836Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32371071A>TCA387752894BRCA2c.8603A>T (p.Lys2868Ile)
c.8234A>T (p.Lys2745Ile)
c.1070A>T (p.Lys357Ile)
c.8611A>T (n.8611A>T)
c.1168A>T
c.101A>T (p.Lys34Ile)
c.8507A>T (p.Lys2836Ile)
 dbSNP
13g.32371072A>CCA387752897BRCA2c.8604A>C (p.Lys2868Asn)
c.8235A>C (p.Lys2745Asn)
c.1071A>C (p.Lys357Asn)
c.8612A>C (n.8612A>C)
c.1169A>C
c.102A>C (p.Lys34Asn)
c.8508A>C (p.Lys2836Asn)
13g.32371072A>GCA483261559BRCA2c.8604A>G (p.Lys2868=)
c.8235A>G (p.Lys2745=)
c.1071A>G (p.Lys357=)
c.8612A>G (n.8612A>G)
c.1169A>G
c.102A>G (p.Lys34=)
c.8508A>G (p.Lys2836=)
13g.32371072A>TCA387752899BRCA2c.8604A>T (p.Lys2868Asn)
c.8235A>T (p.Lys2745Asn)
c.1071A>T (p.Lys357Asn)
c.8612A>T (n.8612A>T)
c.1169A>T
c.102A>T (p.Lys34Asn)
c.8508A>T (p.Lys2836Asn)
 dbSNP
13g.32371073A=CA2082816407BRCA2c.8605A= (p.Ile2869=)
c.8236A= (p.Ile2746=)
c.1072A= (p.Ile358=)
c.8613A= (n.8613A=)
c.1170A=
c.103A= (p.Ile35=)
c.8509A= (p.Ile2837=)
13g.32371073A>CCA387752901BRCA2c.8605A>C (p.Ile2869Leu)
c.8236A>C (p.Ile2746Leu)
c.1072A>C (p.Ile358Leu)
c.8613A>C (n.8613A>C)
c.1170A>C
c.103A>C (p.Ile35Leu)
c.8509A>C (p.Ile2837Leu)
 ClinVar dbSNP gnomAD v4
13g.32371073A>GCA387752903BRCA2c.8605A>G (p.Ile2869Val)
c.8236A>G (p.Ile2746Val)
c.1072A>G (p.Ile358Val)
c.8613A>G (n.8613A>G)
c.1170A>G
c.103A>G (p.Ile35Val)
c.8509A>G (p.Ile2837Val)
 ClinVar
13g.32371073A>TCA387752905BRCA2c.8605A>T (p.Ile2869Phe)
c.8236A>T (p.Ile2746Phe)
c.1072A>T (p.Ile358Phe)
c.8613A>T (n.8613A>T)
c.1170A>T
c.103A>T (p.Ile35Phe)
c.8509A>T (p.Ile2837Phe)
13g.32371073_32371074delinsATCA2082816405BRCA2c.8605_8606delinsAT (p.Ile2869=)
c.8236_8237delinsAT (p.Ile2746=)
c.1072_1073delinsAT (p.Ile358=)
c.8613_8614delinsAT (n.8613_8614delinsAT)
c.1170_1171delinsAT
c.103_104delinsAT (p.Ile35=)
c.8509_8510delinsAT (p.Ile2837=)
13g.32371074T>ACA387752907BRCA2c.8606T>A (p.Ile2869Asn)
c.8237T>A (p.Ile2746Asn)
c.1073T>A (p.Ile358Asn)
c.8614T>A (n.8614T>A)
c.1171T>A
c.104T>A (p.Ile35Asn)
c.8510T>A (p.Ile2837Asn)
 ClinVar dbSNP
13g.32371074T>CCA387752909BRCA2c.8606T>C (p.Ile2869Thr)
c.8237T>C (p.Ile2746Thr)
c.1073T>C (p.Ile358Thr)
c.8614T>C (n.8614T>C)
c.1171T>C
c.104T>C (p.Ile35Thr)
c.8510T>C (p.Ile2837Thr)
13g.32371074T>GCA387752910BRCA2c.8606T>G (p.Ile2869Ser)
c.8237T>G (p.Ile2746Ser)
c.1073T>G (p.Ile358Ser)
c.8614T>G (n.8614T>G)
c.1171T>G
c.104T>G (p.Ile35Ser)
c.8510T>G (p.Ile2837Ser)
13g.32371074T=CA2082816419BRCA2c.8606T= (p.Ile2869=)
c.8237T= (p.Ile2746=)
c.1073T= (p.Ile358=)
c.8614T= (n.8614T=)
c.1171T=
c.104T= (p.Ile35=)
c.8510T= (p.Ile2837=)
13g.32371074_32371075delCA2580087403BRCA2c.8606_8607del (p.Ile2869ThrfsTer5)
c.8237_8238del (p.Ile2746ThrfsTer5)
c.1073_1074del (p.Ile358ThrfsTer5)
c.8614_8615del (n.8614_8615del)
c.1171_1172del
c.104_105del (p.Ile35ThrfsTer5)
c.8510_8511del (p.Ile2837ThrfsTer5)
 ClinVar
13g.32371075delCA16614011BRCA2c.8607del (p.Gln2870ArgfsTer21)
c.8607del (p.Gln2870ArgfsTer16)
c.8238del (p.Gln2747ArgfsTer21)
c.8607del (p.Gln2870ArgfsTer22)
c.1074del (p.Gln359ArgfsTer21)
c.8615del (n.8615del)
c.1172del
c.105del (p.Gln36ArgfsTer16)
c.8511del (p.Gln2838ArgfsTer21)
 ClinVar dbSNP
13g.32371075T>ACA16613967BRCA2c.8607T>A (p.Ile2869=)
c.8238T>A (p.Ile2746=)
c.1074T>A (p.Ile358=)
c.8615T>A (n.8615T>A)
c.1172T>A
c.105T>A (p.Ile35=)
c.8511T>A (p.Ile2837=)
 ClinVar dbSNP gnomAD v4
13g.32371075T>CCA025732BRCA2c.8607T>C (p.Ile2869=)
c.8238T>C (p.Ile2746=)
c.1074T>C (p.Ile358=)
c.8615T>C (n.8615T>C)
c.1172T>C
c.105T>C (p.Ile35=)
c.8511T>C (p.Ile2837=)
 ClinVar dbSNP
13g.32371075T>GCA387752911BRCA2c.8607T>G (p.Ile2869Met)
c.8238T>G (p.Ile2746Met)
c.1074T>G (p.Ile358Met)
c.8615T>G (n.8615T>G)
c.1172T>G
c.105T>G (p.Ile35Met)
c.8511T>G (p.Ile2837Met)
13g.32371075T=CA2082816432BRCA2c.8607T= (p.Ile2869=)
c.8238T= (p.Ile2746=)
c.1074T= (p.Ile358=)
c.8615T= (n.8615T=)
c.1172T=
c.105T= (p.Ile35=)
c.8511T= (p.Ile2837=)
13g.32371076C>ACA387752912BRCA2c.8608C>A (p.Gln2870Lys)
c.8239C>A (p.Gln2747Lys)
c.1075C>A (p.Gln359Lys)
c.8616C>A (n.8616C>A)
c.1173C>A
c.106C>A (p.Gln36Lys)
c.8512C>A (p.Gln2838Lys)
13g.32371076C=CA2082816439BRCA2c.8608C= (p.Gln2870=)
c.8239C= (p.Gln2747=)
c.1075C= (p.Gln359=)
c.8616C= (n.8616C=)
c.1173C=
c.106C= (p.Gln36=)
c.8512C= (p.Gln2838=)
13g.32371076C>GCA387752913BRCA2c.8608C>G (p.Gln2870Glu)
c.8239C>G (p.Gln2747Glu)
c.1075C>G (p.Gln359Glu)
c.8616C>G (n.8616C>G)
c.1173C>G
c.106C>G (p.Gln36Glu)
c.8512C>G (p.Gln2838Glu)
 dbSNP gnomAD v4
13g.32371076C>TCA025733BRCA2c.8608C>T (p.Gln2870Ter)
c.8239C>T (p.Gln2747Ter)
c.1075C>T (p.Gln359Ter)
c.8616C>T (n.8616C>T)
c.1173C>T
c.106C>T (p.Gln36Ter)
c.8512C>T (p.Gln2838Ter)
 ClinVar dbSNP COSMIC COSMIC
13g.32371077A>CCA387752918BRCA2c.8609A>C (p.Gln2870Pro)
c.8240A>C (p.Gln2747Pro)
c.1076A>C (p.Gln359Pro)
c.8617A>C (n.8617A>C)
c.1174A>C
c.107A>C (p.Gln36Pro)
c.8513A>C (p.Gln2838Pro)
13g.32371077A>GCA387752914BRCA2c.8609A>G (p.Gln2870Arg)
c.8240A>G (p.Gln2747Arg)
c.1076A>G (p.Gln359Arg)
c.8617A>G (n.8617A>G)
c.1174A>G
c.107A>G (p.Gln36Arg)
c.8513A>G (p.Gln2838Arg)
 ClinVar dbSNP gnomAD v4
13g.32371077A>TCA387752916BRCA2c.8609A>T (p.Gln2870Leu)
c.8240A>T (p.Gln2747Leu)
c.1076A>T (p.Gln359Leu)
c.8617A>T (n.8617A>T)
c.1174A>T
c.107A>T (p.Gln36Leu)
c.8513A>T (p.Gln2838Leu)
13g.32371078G>ACA483261560BRCA2c.8610G>A (p.Gln2870=)
c.8241G>A (p.Gln2747=)
c.1077G>A (p.Gln359=)
c.8618G>A (n.8618G>A)
c.1175G>A
c.108G>A (p.Gln36=)
c.8514G>A (p.Gln2838=)
 dbSNP gnomAD v3 gnomAD v4
13g.32371078G>CCA387752921BRCA2c.8610G>C (p.Gln2870His)
c.8241G>C (p.Gln2747His)
c.1077G>C (p.Gln359His)
c.8618G>C (n.8618G>C)
c.1175G>C
c.108G>C (p.Gln36His)
c.8514G>C (p.Gln2838His)
 ClinVar dbSNP
13g.32371078G=CA2082816446BRCA2c.8610G= (p.Gln2870=)
c.8241G= (p.Gln2747=)
c.1077G= (p.Gln359=)
c.8618G= (n.8618G=)
c.1175G=
c.108G= (p.Gln36=)
c.8514G= (p.Gln2838=)
13g.32371078G>TCA387752922BRCA2c.8610G>T (p.Gln2870His)
c.8241G>T (p.Gln2747His)
c.1077G>T (p.Gln359His)
c.8618G>T (n.8618G>T)
c.1175G>T
c.108G>T (p.Gln36His)
c.8514G>T (p.Gln2838His)
 dbSNP
13g.32371079G>ACA387752925BRCA2c.8611G>A (p.Glu2871Lys)
c.8242G>A (p.Glu2748Lys)
c.1078G>A (p.Glu360Lys)
c.8619G>A (n.8619G>A)
c.1176G>A
c.109G>A (p.Glu37Lys)
c.8515G>A (p.Glu2839Lys)
 ClinVar dbSNP gnomAD v4
13g.32371079G>CCA025734BRCA2c.8611G>C (p.Glu2871Gln)
c.8242G>C (p.Glu2748Gln)
c.1078G>C (p.Glu360Gln)
c.8619G>C (n.8619G>C)
c.1176G>C
c.109G>C (p.Glu37Gln)
c.8515G>C (p.Glu2839Gln)
 ClinVar dbSNP
13g.32371079G=CA2082816458BRCA2c.8611G= (p.Glu2871=)
c.8242G= (p.Glu2748=)
c.1078G= (p.Glu360=)
c.8619G= (n.8619G=)
c.1176G=
c.109G= (p.Glu37=)
c.8515G= (p.Glu2839=)
13g.32371079G>TCA387752927BRCA2c.8611G>T (p.Glu2871Ter)
c.8242G>T (p.Glu2748Ter)
c.1078G>T (p.Glu360Ter)
c.8619G>T (n.8619G>T)
c.1176G>T
c.109G>T (p.Glu37Ter)
c.8515G>T (p.Glu2839Ter)
 ClinVar dbSNP
13g.32371080A=CA2082816464BRCA2c.8612A= (p.Glu2871=)
c.8243A= (p.Glu2748=)
c.1079A= (p.Glu360=)
c.8620A= (n.8620A=)
c.1177A=
c.110A= (p.Glu37=)
c.8516A= (p.Glu2839=)
13g.32371080A>CCA387752928BRCA2c.8612A>C (p.Glu2871Ala)
c.8243A>C (p.Glu2748Ala)
c.1079A>C (p.Glu360Ala)
c.8620A>C (n.8620A>C)
c.1177A>C
c.110A>C (p.Glu37Ala)
c.8516A>C (p.Glu2839Ala)
 ClinVar dbSNP
13g.32371080A>GCA387752930BRCA2c.8612A>G (p.Glu2871Gly)
c.8243A>G (p.Glu2748Gly)
c.1079A>G (p.Glu360Gly)
c.8620A>G (n.8620A>G)
c.1177A>G
c.110A>G (p.Glu37Gly)
c.8516A>G (p.Glu2839Gly)
 ClinVar dbSNP
13g.32371080A>TCA387752932BRCA2c.8612A>T (p.Glu2871Val)
c.8243A>T (p.Glu2748Val)
c.1079A>T (p.Glu360Val)
c.8620A>T (n.8620A>T)
c.1177A>T
c.110A>T (p.Glu37Val)
c.8516A>T (p.Glu2839Val)
 dbSNP
13g.32371081G>ACA483261561BRCA2c.8613G>A (p.Glu2871=)
c.8244G>A (p.Glu2748=)
c.1080G>A (p.Glu360=)
c.8621G>A (n.8621G>A)
c.1178G>A
c.111G>A (p.Glu37=)
c.8517G>A (p.Glu2839=)
 ClinVar dbSNP
13g.32371081G>CCA387752934BRCA2c.8613G>C (p.Glu2871Asp)
c.8244G>C (p.Glu2748Asp)
c.1080G>C (p.Glu360Asp)
c.8621G>C (n.8621G>C)
c.1178G>C
c.111G>C (p.Glu37Asp)
c.8517G>C (p.Glu2839Asp)
 ClinVar dbSNP
13g.32371081G=CA2082816478BRCA2c.8613G= (p.Glu2871=)
c.8244G= (p.Glu2748=)
c.1080G= (p.Glu360=)
c.8621G= (n.8621G=)
c.1178G=
c.111G= (p.Glu37=)
c.8517G= (p.Glu2839=)
13g.32371081G>TCA387752936BRCA2c.8613G>T (p.Glu2871Asp)
c.8244G>T (p.Glu2748Asp)
c.1080G>T (p.Glu360Asp)
c.8621G>T (n.8621G>T)
c.1178G>T
c.111G>T (p.Glu37Asp)
c.8517G>T (p.Glu2839Asp)
 dbSNP
13g.32371081_32371082insTCA1139770806BRCA2c.8613_8614insT (p.Glu2872Ter)
c.8244_8245insT (p.Glu2749Ter)
c.1080_1081insT (p.Glu361Ter)
c.8621_8622insT (n.8621_8622insT)
c.1178_1179insT
c.111_112insT (p.Glu38Ter)
c.8517_8518insT (p.Glu2840Ter)
13g.32371082G>ACA387752940BRCA2c.8614G>A (p.Glu2872Lys)
c.8245G>A (p.Glu2749Lys)
c.1081G>A (p.Glu361Lys)
c.8622G>A (n.8622G>A)
c.1179G>A
c.112G>A (p.Glu38Lys)
c.8518G>A (p.Glu2840Lys)
 ClinVar dbSNP gnomAD v4
13g.32371082G>CCA387752942BRCA2c.8614G>C (p.Glu2872Gln)
c.8245G>C (p.Glu2749Gln)
c.1081G>C (p.Glu361Gln)
c.8622G>C (n.8622G>C)
c.1179G>C
c.112G>C (p.Glu38Gln)
c.8518G>C (p.Glu2840Gln)
 dbSNP
13g.32371082G=CA2082816490BRCA2c.8614G= (p.Glu2872=)
c.8245G= (p.Glu2749=)
c.1081G= (p.Glu361=)
c.8622G= (n.8622G=)
c.1179G=
c.112G= (p.Glu38=)
c.8518G= (p.Glu2840=)
13g.32371082G>TCA387752938BRCA2c.8614G>T (p.Glu2872Ter)
c.8245G>T (p.Glu2749Ter)
c.1081G>T (p.Glu361Ter)
c.8622G>T (n.8622G>T)
c.1179G>T
c.112G>T (p.Glu38Ter)
c.8518G>T (p.Glu2840Ter)
 ClinVar dbSNP
13g.32371083A=CA2082816496BRCA2c.8615A= (p.Glu2872=)
c.8246A= (p.Glu2749=)
c.1082A= (p.Glu361=)
c.8623A= (n.8623A=)
c.1180A=
c.113A= (p.Glu38=)
c.8519A= (p.Glu2840=)
13g.32371083A>CCA387752943BRCA2c.8615A>C (p.Glu2872Ala)
c.8246A>C (p.Glu2749Ala)
c.1082A>C (p.Glu361Ala)
c.8623A>C (n.8623A>C)
c.1180A>C
c.113A>C (p.Glu38Ala)
c.8519A>C (p.Glu2840Ala)
13g.32371083A>GCA387752944BRCA2c.8615A>G (p.Glu2872Gly)
c.8246A>G (p.Glu2749Gly)
c.1082A>G (p.Glu361Gly)
c.8623A>G (n.8623A>G)
c.1180A>G
c.113A>G (p.Glu38Gly)
c.8519A>G (p.Glu2840Gly)
 ClinVar dbSNP
13g.32371083A>TCA387752945BRCA2c.8615A>T (p.Glu2872Val)
c.8246A>T (p.Glu2749Val)
c.1082A>T (p.Glu361Val)
c.8623A>T (n.8623A>T)
c.1180A>T
c.113A>T (p.Glu38Val)
c.8519A>T (p.Glu2840Val)
 ClinVar dbSNP
13g.32371084A>CCA387752948BRCA2c.8616A>C (p.Glu2872Asp)
c.8247A>C (p.Glu2749Asp)
c.1083A>C (p.Glu361Asp)
c.8624A>C (n.8624A>C)
c.1181A>C
c.114A>C (p.Glu38Asp)
c.8520A>C (p.Glu2840Asp)
13g.32371084A>GCA483261562BRCA2c.8616A>G (p.Glu2872=)
c.8247A>G (p.Glu2749=)
c.1083A>G (p.Glu361=)
c.8624A>G (n.8624A>G)
c.1181A>G
c.114A>G (p.Glu38=)
c.8520A>G (p.Glu2840=)
13g.32371084A>TCA387752949BRCA2c.8616A>T (p.Glu2872Asp)
c.8247A>T (p.Glu2749Asp)
c.1083A>T (p.Glu361Asp)
c.8624A>T (n.8624A>T)
c.1181A>T
c.114A>T (p.Glu38Asp)
c.8520A>T (p.Glu2840Asp)
13g.32371085T>ACA387752955BRCA2c.8617T>A (p.Phe2873Ile)
c.8248T>A (p.Phe2750Ile)
c.1084T>A (p.Phe362Ile)
c.8625T>A (n.8625T>A)
c.1182T>A
c.115T>A (p.Phe39Ile)
c.8521T>A (p.Phe2841Ile)
 dbSNP
13g.32371085T>CCA387752951BRCA2c.8617T>C (p.Phe2873Leu)
c.8248T>C (p.Phe2750Leu)
c.1084T>C (p.Phe362Leu)
c.8625T>C (n.8625T>C)
c.1182T>C
c.115T>C (p.Phe39Leu)
c.8521T>C (p.Phe2841Leu)
13g.32371085T>GCA387752953BRCA2c.8617T>G (p.Phe2873Val)
c.8248T>G (p.Phe2750Val)
c.1084T>G (p.Phe362Val)
c.8625T>G (n.8625T>G)
c.1182T>G
c.115T>G (p.Phe39Val)
c.8521T>G (p.Phe2841Val)
 dbSNP
13g.32371087dupCA2727921503BRCA2c.8619dup (p.Glu2874Ter)
c.8250dup (p.Glu2751Ter)
c.1086dup (p.Glu363Ter)
c.8627dup (n.8627dup)
c.1184dup
c.117dup (p.Glu40Ter)
c.8523dup (p.Glu2842Ter)
 dbSNP
13g.32371086T>ACA387752957BRCA2c.8618T>A (p.Phe2873Tyr)
c.8249T>A (p.Phe2750Tyr)
c.1085T>A (p.Phe362Tyr)
c.8626T>A (n.8626T>A)
c.1183T>A
c.116T>A (p.Phe39Tyr)
c.8522T>A (p.Phe2841Tyr)
 dbSNP
13g.32371086T>CCA387752959BRCA2c.8618T>C (p.Phe2873Ser)
c.8249T>C (p.Phe2750Ser)
c.1085T>C (p.Phe362Ser)
c.8626T>C (n.8626T>C)
c.1183T>C
c.116T>C (p.Phe39Ser)
c.8522T>C (p.Phe2841Ser)
 ClinVar
13g.32371086T>GCA025735BRCA2c.8618T>G (p.Phe2873Cys)
c.8249T>G (p.Phe2750Cys)
c.1085T>G (p.Phe362Cys)
c.8626T>G (n.8626T>G)
c.1183T>G
c.116T>G (p.Phe39Cys)
c.8522T>G (p.Phe2841Cys)
 ClinVar dbSNP gnomAD v4
13g.32371086T=CA2082816504BRCA2c.8618T= (p.Phe2873=)
c.8249T= (p.Phe2750=)
c.1085T= (p.Phe362=)
c.8626T= (n.8626T=)
c.1183T=
c.116T= (p.Phe39=)
c.8522T= (p.Phe2841=)
13g.32371087T>ACA6941263BRCA2c.8619T>A (p.Phe2873Leu)
c.8250T>A (p.Phe2750Leu)
c.1086T>A (p.Phe362Leu)
c.8627T>A (n.8627T>A)
c.1184T>A
c.117T>A (p.Phe39Leu)
c.8523T>A (p.Phe2841Leu)
 dbSNP ExAC
13g.32371087T>CCA483261563BRCA2c.8619T>C (p.Phe2873=)
c.8250T>C (p.Phe2750=)
c.1086T>C (p.Phe362=)
c.8627T>C (n.8627T>C)
c.1184T>C
c.117T>C (p.Phe39=)
c.8523T>C (p.Phe2841=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32371087T>GCA387752965BRCA2c.8619T>G (p.Phe2873Leu)
c.8250T>G (p.Phe2750Leu)
c.1086T>G (p.Phe362Leu)
c.8627T>G (n.8627T>G)
c.1184T>G
c.117T>G (p.Phe39Leu)
c.8523T>G (p.Phe2841Leu)
13g.32371087T=CA2082816522BRCA2c.8619T= (p.Phe2873=)
c.8250T= (p.Phe2750=)
c.1086T= (p.Phe362=)
c.8627T= (n.8627T=)
c.1184T=
c.117T= (p.Phe39=)
c.8523T= (p.Phe2841=)
13g.32371088G>ACA387752967BRCA2c.8620G>A (p.Glu2874Lys)
c.8251G>A (p.Glu2751Lys)
c.1087G>A (p.Glu363Lys)
c.8628G>A (n.8628G>A)
c.1185G>A
c.118G>A (p.Glu40Lys)
c.8524G>A (p.Glu2842Lys)
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32371088G>CCA387752970BRCA2c.8620G>C (p.Glu2874Gln)
c.8251G>C (p.Glu2751Gln)
c.1087G>C (p.Glu363Gln)
c.8628G>C (n.8628G>C)
c.1185G>C
c.118G>C (p.Glu40Gln)
c.8524G>C (p.Glu2842Gln)
 dbSNP
13g.32371088G=CA2082816529BRCA2c.8620G= (p.Glu2874=)
c.8251G= (p.Glu2751=)
c.1087G= (p.Glu363=)
c.8628G= (n.8628G=)
c.1185G=
c.118G= (p.Glu40=)
c.8524G= (p.Glu2842=)
13g.32371088G>TCA025736BRCA2c.8620G>T (p.Glu2874Ter)
c.8251G>T (p.Glu2751Ter)
c.1087G>T (p.Glu363Ter)
c.8628G>T (n.8628G>T)
c.1185G>T
c.118G>T (p.Glu40Ter)
c.8524G>T (p.Glu2842Ter)
 ClinVar dbSNP
13g.32371089A>CCA387752971BRCA2c.8621A>C (p.Glu2874Ala)
c.8252A>C (p.Glu2751Ala)
c.1088A>C (p.Glu363Ala)
c.8629A>C (n.8629A>C)
c.1186A>C
c.119A>C (p.Glu40Ala)
c.8525A>C (p.Glu2842Ala)
13g.32371089A>GCA387752974BRCA2c.8621A>G (p.Glu2874Gly)
c.8252A>G (p.Glu2751Gly)
c.1088A>G (p.Glu363Gly)
c.8629A>G (n.8629A>G)
c.1186A>G
c.119A>G (p.Glu40Gly)
c.8525A>G (p.Glu2842Gly)
 dbSNP COSMIC COSMIC
13g.32371089A>TCA387752976BRCA2c.8621A>T (p.Glu2874Val)
c.8252A>T (p.Glu2751Val)
c.1088A>T (p.Glu363Val)
c.8629A>T (n.8629A>T)
c.1186A>T
c.119A>T (p.Glu40Val)
c.8525A>T (p.Glu2842Val)
 dbSNP
13g.32371090dupCA2573149216BRCA2c.8622dup (p.Glu2875ArgfsTer3)
c.8253dup (p.Glu2752ArgfsTer3)
c.1089dup (p.Glu364ArgfsTer3)
c.8630dup (n.8630dup)
c.1187dup
c.120dup (p.Glu41ArgfsTer3)
c.8526dup (p.Glu2843ArgfsTer3)
 ClinVar dbSNP
13g.32371090delCA2580087405BRCA2c.8622del (p.Glu2875AsnfsTer16)
c.8622del (p.Glu2875AsnfsTer11)
c.8253del (p.Glu2752AsnfsTer16)
c.8622del (p.Glu2875AsnfsTer17)
c.1089del (p.Glu364AsnfsTer16)
c.8630del (n.8630del)
c.1187del
c.120del (p.Glu41AsnfsTer11)
c.8526del (p.Glu2843AsnfsTer16)
 ClinVar
13g.32371090A>CCA387752978BRCA2c.8622A>C (p.Glu2874Asp)
c.8253A>C (p.Glu2751Asp)
c.1089A>C (p.Glu363Asp)
c.8630A>C (n.8630A>C)
c.1187A>C
c.120A>C (p.Glu40Asp)
c.8526A>C (p.Glu2842Asp)
13g.32371090A>GCA483261564BRCA2c.8622A>G (p.Glu2874=)
c.8253A>G (p.Glu2751=)
c.1089A>G (p.Glu363=)
c.8630A>G (n.8630A>G)
c.1187A>G
c.120A>G (p.Glu40=)
c.8526A>G (p.Glu2842=)
 dbSNP
13g.32371090A>TCA387752979BRCA2c.8622A>T (p.Glu2874Asp)
c.8253A>T (p.Glu2751Asp)
c.1089A>T (p.Glu363Asp)
c.8630A>T (n.8630A>T)
c.1187A>T
c.120A>T (p.Glu40Asp)
c.8526A>T (p.Glu2842Asp)
 dbSNP
13g.32371091delCA2580087407BRCA2c.8623del (p.Glu2875AsnfsTer16)
c.8623del (p.Glu2875AsnfsTer11)
c.8254del (p.Glu2752AsnfsTer16)
c.8623del (p.Glu2875AsnfsTer17)
c.1090del (p.Glu364AsnfsTer16)
c.8631del (n.8631del)
c.1188del
c.121del (p.Glu41AsnfsTer11)
c.8527del (p.Glu2843AsnfsTer16)
 ClinVar
13g.32371091G>ACA387752980BRCA2c.8623G>A (p.Glu2875Lys)
c.8254G>A (p.Glu2752Lys)
c.1090G>A (p.Glu364Lys)
c.8631G>A (n.8631G>A)
c.1188G>A
c.121G>A (p.Glu41Lys)
c.8527G>A (p.Glu2843Lys)
 ClinVar dbSNP gnomAD v4
13g.32371091G>CCA387752981BRCA2c.8623G>C (p.Glu2875Gln)
c.8254G>C (p.Glu2752Gln)
c.1090G>C (p.Glu364Gln)
c.8631G>C (n.8631G>C)
c.1188G>C
c.121G>C (p.Glu41Gln)
c.8527G>C (p.Glu2843Gln)
 dbSNP
13g.32371091G>TCA387752982BRCA2c.8623G>T (p.Glu2875Ter)
c.8254G>T (p.Glu2752Ter)
c.1090G>T (p.Glu364Ter)
c.8631G>T (n.8631G>T)
c.1188G>T
c.121G>T (p.Glu41Ter)
c.8527G>T (p.Glu2843Ter)
 dbSNP
13g.32371092A>CCA387752983BRCA2c.8624A>C (p.Glu2875Ala)
c.8255A>C (p.Glu2752Ala)
c.1091A>C (p.Glu364Ala)
c.8632A>C (n.8632A>C)
c.1189A>C
c.122A>C (p.Glu41Ala)
c.8528A>C (p.Glu2843Ala)
13g.32371092A>GCA387752988BRCA2c.8624A>G (p.Glu2875Gly)
c.8255A>G (p.Glu2752Gly)
c.1091A>G (p.Glu364Gly)
c.8632A>G (n.8632A>G)
c.1189A>G
c.122A>G (p.Glu41Gly)
c.8528A>G (p.Glu2843Gly)
 dbSNP
13g.32371092A>TCA387752992BRCA2c.8624A>T (p.Glu2875Val)
c.8255A>T (p.Glu2752Val)
c.1091A>T (p.Glu364Val)
c.8632A>T (n.8632A>T)
c.1189A>T
c.122A>T (p.Glu41Val)
c.8528A>T (p.Glu2843Val)
 dbSNP
13g.32371093A=CA2082816540BRCA2c.8625A= (p.Glu2875=)
c.8256A= (p.Glu2752=)
c.1092A= (p.Glu364=)
c.8633A= (n.8633A=)
c.1190A=
c.123A= (p.Glu41=)
c.8529A= (p.Glu2843=)
13g.32371093A>CCA387752997BRCA2c.8625A>C (p.Glu2875Asp)
c.8256A>C (p.Glu2752Asp)
c.1092A>C (p.Glu364Asp)
c.8633A>C (n.8633A>C)
c.1190A>C
c.123A>C (p.Glu41Asp)
c.8529A>C (p.Glu2843Asp)
 ClinVar dbSNP
13g.32371093A>GCA483261565BRCA2c.8625A>G (p.Glu2875=)
c.8256A>G (p.Glu2752=)
c.1092A>G (p.Glu364=)
c.8633A>G (n.8633A>G)
c.1190A>G
c.123A>G (p.Glu41=)
c.8529A>G (p.Glu2843=)
 ClinVar dbSNP
13g.32371093A>TCA387752995BRCA2c.8625A>T (p.Glu2875Asp)
c.8256A>T (p.Glu2752Asp)
c.1092A>T (p.Glu364Asp)
c.8633A>T (n.8633A>T)
c.1190A>T
c.123A>T (p.Glu41Asp)
c.8529A>T (p.Glu2843Asp)

Number of alleles fetched