Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32338197_32338391del | CA2580618074 | BRCA2 | c.3842_4036del (p.Lys1281_Asp1345del) c.3473_3667del (p.Lys1158_Asp1222del) n.3842_4036del | |
13 | g.32338361_32338405dup | CA913188559 | BRCA2 | c.4006_4050dup (p.His1350_Lys1351insPheAspGlySerAspSerSerLysAsnAspThrValCysIleHis) c.3637_3681dup (p.His1227_Lys1228insPheAspGlySerAspSerSerLysAsnAspThrValCysIleHis) n.4006_4050dup | ClinVar dbSNP |
13 | g.32338363T>A | CA387779010 | BRCA2 | c.4008T>A (p.Phe1336Leu) c.3639T>A (p.Phe1213Leu) n.4008T>A | |
13 | g.32338363T>C | CA483438025 | BRCA2 | c.4008T>C (p.Phe1336=) c.3639T>C (p.Phe1213=) n.4008T>C | ClinVar dbSNP |
13 | g.32338363T>G | CA387779011 | BRCA2 | c.4008T>G (p.Phe1336Leu) c.3639T>G (p.Phe1213Leu) n.4008T>G | |
13 | g.32338363T= | CA2082822884 | BRCA2 | c.4008T= (p.Phe1336=) c.3639T= (p.Phe1213=) n.4008T= | |
13 | g.32338363_32338364insCATC | CA019388 | BRCA2 | c.4008_4009insCATC (p.Asp1337HisfsTer5) c.3639_3640insCATC (p.Asp1214HisfsTer5) n.4008_4009insCATC | ClinVar dbSNP |
13 | g.32338364G>A | CA387779014 | BRCA2 | c.4009G>A (p.Asp1337Asn) c.3640G>A (p.Asp1214Asn) n.4009G>A | dbSNP |
13 | g.32338364G>C | CA387779013 | BRCA2 | c.4009G>C (p.Asp1337His) c.3640G>C (p.Asp1214His) n.4009G>C | dbSNP |
13 | g.32338364G>T | CA387779012 | BRCA2 | c.4009G>T (p.Asp1337Tyr) c.3640G>T (p.Asp1214Tyr) n.4009G>T | ClinVar dbSNP gnomAD v4 |
13 | g.32338365A= | CA2082822905 | BRCA2 | c.4010A= (p.Asp1337=) c.3641A= (p.Asp1214=) n.4010A= | |
13 | g.32338365A>C | CA387779015 | BRCA2 | c.4010A>C (p.Asp1337Ala) c.3641A>C (p.Asp1214Ala) n.4010A>C | ClinVar |
13 | g.32338365A>G | CA387779016 | BRCA2 | c.4010A>G (p.Asp1337Gly) c.3641A>G (p.Asp1214Gly) n.4010A>G | ClinVar dbSNP gnomAD v4 |
13 | g.32338365A>T | CA387779017 | BRCA2 | c.4010A>T (p.Asp1337Val) c.3641A>T (p.Asp1214Val) n.4010A>T | ClinVar dbSNP |
13 | g.32338366T>A | CA387779018 | BRCA2 | c.4011T>A (p.Asp1337Glu) c.3642T>A (p.Asp1214Glu) n.4011T>A | |
13 | g.32338366T>C | CA483438028 | BRCA2 | c.4011T>C (p.Asp1337=) c.3642T>C (p.Asp1214=) n.4011T>C | gnomAD v4 |
13 | g.32338366T>G | CA387779019 | BRCA2 | c.4011T>G (p.Asp1337Glu) c.3642T>G (p.Asp1214Glu) n.4011T>G | ClinVar dbSNP gnomAD v4 |
13 | g.32338366T= | CA2082822918 | BRCA2 | c.4011T= (p.Asp1337=) c.3642T= (p.Asp1214=) n.4011T= | |
13 | g.32338366_32338367delinsTG | CA2082822911 | BRCA2 | c.4011_4012delinsTG (p.Asp1337=) c.3642_3643delinsTG (p.Asp1214=) n.4011_4012delinsTG | |
13 | g.32338367G>A | CA387779020 | BRCA2 | c.4012G>A (p.Gly1338Ser) c.3643G>A (p.Gly1215Ser) n.4012G>A | ClinVar dbSNP |
13 | g.32338367G>C | CA387779021 | BRCA2 | c.4012G>C (p.Gly1338Arg) c.3643G>C (p.Gly1215Arg) n.4012G>C | dbSNP |
13 | g.32338367G= | CA2082822933 | BRCA2 | c.4012G= (p.Gly1338=) c.3643G= (p.Gly1215=) n.4012G= | |
13 | g.32338367G>T | CA387779022 | BRCA2 | c.4012G>T (p.Gly1338Cys) c.3643G>T (p.Gly1215Cys) n.4012G>T | dbSNP gnomAD v4 |
13 | g.32338367_32338368dup | CA658823561 | BRCA2 | c.4012_4013dup (p.Ser1339AlafsTer?) c.3643_3644dup (p.Ser1216AlafsTer?) n.4012_4013dup | ClinVar dbSNP |
13 | g.32338368del | CA019392 | BRCA2 | c.4013del (p.Gly1338AlafsTer?) c.3644del (p.Gly1215AlafsTer?) n.4013del | ClinVar dbSNP |
13 | g.32338367_32338369delinsGGC | CA2082822942 | BRCA2 | c.4012_4014delinsGGC (p.Gly1338=) c.3643_3645delinsGGC (p.Gly1215=) n.4012_4014delinsGGC | |
13 | g.32338368G>A | CA387779023 | BRCA2 | c.4013G>A (p.Gly1338Asp) c.3644G>A (p.Gly1215Asp) n.4013G>A | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
13 | g.32338368G>C | CA387779024 | BRCA2 | c.4013G>C (p.Gly1338Ala) c.3644G>C (p.Gly1215Ala) n.4013G>C | dbSNP |
13 | g.32338368G>T | CA387779025 | BRCA2 | c.4013G>T (p.Gly1338Val) c.3644G>T (p.Gly1215Val) n.4013G>T | ClinVar dbSNP |
13 | g.32338368_32338369del | CA658656332 | BRCA2 | c.4013_4014del (p.Gly1338GlufsTer2) c.3644_3645del (p.Gly1215GlufsTer2) n.4013_4014del | ClinVar dbSNP |
13 | g.32338369C>A | CA483438036 | BRCA2 | c.4014C>A (p.Gly1338=) c.3645C>A (p.Gly1215=) n.4014C>A | dbSNP gnomAD v4 |
13 | g.32338369C= | CA2082822955 | BRCA2 | c.4014C= (p.Gly1338=) c.3645C= (p.Gly1215=) n.4014C= | |
13 | g.32338369C>G | CA483438033 | BRCA2 | c.4014C>G (p.Gly1338=) c.3645C>G (p.Gly1215=) n.4014C>G | dbSNP |
13 | g.32338369C>T | CA483438035 | BRCA2 | c.4014C>T (p.Gly1338=) c.3645C>T (p.Gly1215=) n.4014C>T | ClinVar dbSNP gnomAD v4 COSMIC |
13 | g.32338369_32338370insGG | CA019398 | BRCA2 | c.4014_4015insGG (p.Ser1339GlyfsTer?) c.3645_3646insGG (p.Ser1216GlyfsTer?) n.4014_4015insGG | ClinVar dbSNP |
13 | g.32338370A>C | CA387779028 | BRCA2 | c.4015A>C (p.Ser1339Arg) c.3646A>C (p.Ser1216Arg) n.4015A>C | |
13 | g.32338370A>G | CA387779026 | BRCA2 | c.4015A>G (p.Ser1339Gly) c.3646A>G (p.Ser1216Gly) n.4015A>G | |
13 | g.32338370A>T | CA387779027 | BRCA2 | c.4015A>T (p.Ser1339Cys) c.3646A>T (p.Ser1216Cys) n.4015A>T | dbSNP |
13 | g.32338371G>A | CA387779029 | BRCA2 | c.4016G>A (p.Ser1339Asn) c.3647G>A (p.Ser1216Asn) n.4016G>A | dbSNP gnomAD v4 |
13 | g.32338371G>C | CA387779030 | BRCA2 | c.4016G>C (p.Ser1339Thr) c.3647G>C (p.Ser1216Thr) n.4016G>C | dbSNP |
13 | g.32338371G>T | CA387779031 | BRCA2 | c.4016G>T (p.Ser1339Ile) c.3647G>T (p.Ser1216Ile) n.4016G>T | ClinVar dbSNP |
13 | g.32338372T>A | CA387779032 | BRCA2 | c.4017T>A (p.Ser1339Arg) c.3648T>A (p.Ser1216Arg) n.4017T>A | dbSNP |
13 | g.32338372T>C | CA483438102 | BRCA2 | c.4017T>C (p.Ser1339=) c.3648T>C (p.Ser1216=) n.4017T>C | ClinVar dbSNP gnomAD v4 |
13 | g.32338372T>G | CA387779033 | BRCA2 | c.4017T>G (p.Ser1339Arg) c.3648T>G (p.Ser1216Arg) n.4017T>G | ClinVar dbSNP |
13 | g.32338372T= | CA2082822966 | BRCA2 | c.4017T= (p.Ser1339=) c.3648T= (p.Ser1216=) n.4017T= | |
13 | g.32338373G>A | CA387779036 | BRCA2 | c.4018G>A (p.Asp1340Asn) c.3649G>A (p.Asp1217Asn) n.4018G>A | dbSNP |
13 | g.32338373G>C | CA387779034 | BRCA2 | c.4018G>C (p.Asp1340His) c.3649G>C (p.Asp1217His) n.4018G>C | dbSNP |
13 | g.32338373G>T | CA387779035 | BRCA2 | c.4018G>T (p.Asp1340Tyr) c.3649G>T (p.Asp1217Tyr) n.4018G>T | gnomAD v4 |
13 | g.32338374A= | CA2082822988 | BRCA2 | c.4019A= (p.Asp1340=) c.3650A= (p.Asp1217=) n.4019A= | |
13 | g.32338374A>C | CA387779037 | BRCA2 | c.4019A>C (p.Asp1340Ala) c.3650A>C (p.Asp1217Ala) n.4019A>C | ClinVar dbSNP |