| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32338531del | CA335700 | BRCA2 | c.4176del (p.Ala1393ArgfsTer17) c.3807del (p.Ala1270ArgfsTer17) n.4176del | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338531T>A | CA483437876 | BRCA2 | c.4176T>A (p.Val1392=) c.3807T>A (p.Val1269=) n.4176T>A | dbSNP |
| 13 | g.32338531T>C | CA483437877 | BRCA2 | c.4176T>C (p.Val1392=) c.3807T>C (p.Val1269=) n.4176T>C | |
| 13 | g.32338531T>G | CA483437878 | BRCA2 | c.4176T>G (p.Val1392=) c.3807T>G (p.Val1269=) n.4176T>G | |
| 13 | g.32338531T= | CA2082809178 | BRCA2 | c.4176T= (p.Val1392=) c.3807T= (p.Val1269=) n.4176T= | |
| 13 | g.32338532G>A | CA387780112 | BRCA2 | c.4177G>A (p.Ala1393Thr) c.3808G>A (p.Ala1270Thr) n.4177G>A | dbSNP |
| 13 | g.32338532G>C | CA387780109 | BRCA2 | c.4177G>C (p.Ala1393Pro) c.3808G>C (p.Ala1270Pro) n.4177G>C | dbSNP |
| 13 | g.32338532G>T | CA387780111 | BRCA2 | c.4177G>T (p.Ala1393Ser) c.3808G>T (p.Ala1270Ser) n.4177G>T | dbSNP |
| 13 | g.32338532dup | CA10579602 | BRCA2 | c.4177dup (p.Ala1393GlyfsTer10) c.3808dup (p.Ala1270GlyfsTer10) n.4177dup | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338533C>A | CA387780113 | BRCA2 | c.4178C>A (p.Ala1393Glu) c.3809C>A (p.Ala1270Glu) n.4178C>A | dbSNP |
| 13 | g.32338533C= | CA2082809188 | BRCA2 | c.4178C= (p.Ala1393=) c.3809C= (p.Ala1270=) n.4178C= | |
| 13 | g.32338533C>G | CA019671 | BRCA2 | c.4178C>G (p.Ala1393Gly) c.3809C>G (p.Ala1270Gly) n.4178C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338533C>T | CA019676 | BRCA2 | c.4178C>T (p.Ala1393Val) c.3809C>T (p.Ala1270Val) n.4178C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 13 | g.32338534G>A | CA019680 | BRCA2 | c.4179G>A (p.Ala1393=) c.3810G>A (p.Ala1270=) n.4179G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 13 | g.32338534G>C | CA483437882 | BRCA2 | c.4179G>C (p.Ala1393=) c.3810G>C (p.Ala1270=) n.4179G>C | ClinVar dbSNP |
| 13 | g.32338534G= | CA2082809208 | BRCA2 | c.4179G= (p.Ala1393=) c.3810G= (p.Ala1270=) n.4179G= | |
| 13 | g.32338534G>T | CA483437883 | BRCA2 | c.4179G>T (p.Ala1393=) c.3810G>T (p.Ala1270=) n.4179G>T | dbSNP |
| 13 | g.32338535A>C | CA387780117 | BRCA2 | c.4180A>C (p.Lys1394Gln) c.3811A>C (p.Lys1271Gln) n.4180A>C | |
| 13 | g.32338535A>G | CA387780118 | BRCA2 | c.4180A>G (p.Lys1394Glu) c.3811A>G (p.Lys1271Glu) n.4180A>G | |
| 13 | g.32338535A>T | CA387780120 | BRCA2 | c.4180A>T (p.Lys1394Ter) c.3811A>T (p.Lys1271Ter) n.4180A>T | dbSNP |
| 13 | g.32338536A>C | CA387780122 | BRCA2 | c.4181A>C (p.Lys1394Thr) c.3812A>C (p.Lys1271Thr) n.4181A>C | |
| 13 | g.32338536A>G | CA387780124 | BRCA2 | c.4181A>G (p.Lys1394Arg) c.3812A>G (p.Lys1271Arg) n.4181A>G | dbSNP |
| 13 | g.32338536A>T | CA387780126 | BRCA2 | c.4181A>T (p.Lys1394Ile) c.3812A>T (p.Lys1271Ile) n.4181A>T | dbSNP |
| 13 | g.32338537A>C | CA387780128 | BRCA2 | c.4182A>C (p.Lys1394Asn) c.3813A>C (p.Lys1271Asn) n.4182A>C | |
| 13 | g.32338537A>G | CA483437886 | BRCA2 | c.4182A>G (p.Lys1394=) c.3813A>G (p.Lys1271=) n.4182A>G | ClinVar dbSNP |
| 13 | g.32338537A>T | CA387780130 | BRCA2 | c.4182A>T (p.Lys1394Asn) c.3813A>T (p.Lys1271Asn) n.4182A>T | dbSNP |
| 13 | g.32338537_32338538delinsAG | CA2082809211 | BRCA2 | c.4182_4183delinsAG (p.Lys1394=) c.3813_3814delinsAG (p.Lys1271=) n.4182_4183delinsAG | |
| 13 | g.32338538del | CA1139663190 | BRCA2 | c.4183del (p.Ala1395LeufsTer15) c.3814del (p.Ala1272LeufsTer15) n.4183del | ClinVar dbSNP |
| 13 | g.32338538G>A | CA387780133 | BRCA2 | c.4183G>A (p.Ala1395Thr) c.3814G>A (p.Ala1272Thr) n.4183G>A | dbSNP |
| 13 | g.32338538G>C | CA387780135 | BRCA2 | c.4183G>C (p.Ala1395Pro) c.3814G>C (p.Ala1272Pro) n.4183G>C | dbSNP |
| 13 | g.32338538G= | CA2082809217 | BRCA2 | c.4183G= (p.Ala1395=) c.3814G= (p.Ala1272=) n.4183G= | |
| 13 | g.32338538G>T | CA019684 | BRCA2 | c.4183G>T (p.Ala1395Ser) c.3814G>T (p.Ala1272Ser) n.4183G>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338539C>A | CA387780141 | BRCA2 | c.4184C>A (p.Ala1395Asp) c.3815C>A (p.Ala1272Asp) n.4184C>A | dbSNP |
| 13 | g.32338539C= | CA2082809231 | BRCA2 | c.4184C= (p.Ala1395=) c.3815C= (p.Ala1272=) n.4184C= | |
| 13 | g.32338539C>G | CA387780137 | BRCA2 | c.4184C>G (p.Ala1395Gly) c.3815C>G (p.Ala1272Gly) n.4184C>G | dbSNP |
| 13 | g.32338539C>T | CA387780139 | BRCA2 | c.4184C>T (p.Ala1395Val) c.3815C>T (p.Ala1272Val) n.4184C>T | ClinVar dbSNP |
| 13 | g.32338539dup | CA2573053809 | BRCA2 | c.4184dup (p.Gln1396SerfsTer7) c.3815dup (p.Gln1273SerfsTer7) n.4184dup | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338540T>A | CA483437891 | BRCA2 | c.4185T>A (p.Ala1395=) c.3816T>A (p.Ala1272=) n.4185T>A | dbSNP |
| 13 | g.32338540T>C | CA483437892 | BRCA2 | c.4185T>C (p.Ala1395=) c.3816T>C (p.Ala1272=) n.4185T>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338540T>G | CA483437894 | BRCA2 | c.4185T>G (p.Ala1395=) c.3816T>G (p.Ala1272=) n.4185T>G | ClinVar dbSNP |
| 13 | g.32338540T= | CA2082809236 | BRCA2 | c.4185T= (p.Ala1395=) c.3816T= (p.Ala1272=) n.4185T= | |
| 13 | g.32338540_32338576del | CA2580087257 | BRCA2 | c.4185_4221del (p.Gln1396SerfsTer2) c.3816_3852del (p.Gln1273SerfsTer2) n.4185_4221del | ClinVar |
| 13 | g.32338541C>A | CA387780143 | BRCA2 | c.4186C>A (p.Gln1396Lys) c.3817C>A (p.Gln1273Lys) n.4186C>A | ClinVar dbSNP |
| 13 | g.32338541C= | CA2082809241 | BRCA2 | c.4186C= (p.Gln1396=) c.3817C= (p.Gln1273=) n.4186C= | |
| 13 | g.32338541C>G | CA6940758 | BRCA2 | c.4186C>G (p.Gln1396Glu) c.3817C>G (p.Gln1273Glu) n.4186C>G | dbSNP ExAC |
| 13 | g.32338541C>T | CA387780145 | BRCA2 | c.4186C>T (p.Gln1396Ter) c.3817C>T (p.Gln1273Ter) n.4186C>T | ClinVar dbSNP |
| 13 | g.32338541_32338542delinsCA | CA2082809240 | BRCA2 | c.4186_4187delinsCA (p.Gln1396=) c.3817_3818delinsCA (p.Gln1273=) n.4186_4187delinsCA | |
| 13 | g.32338542A= | CA2082809249 | BRCA2 | c.4187A= (p.Gln1396=) c.3818A= (p.Gln1273=) n.4187A= | |
| 13 | g.32338542A>C | CA387780151 | BRCA2 | c.4187A>C (p.Gln1396Pro) c.3818A>C (p.Gln1273Pro) n.4187A>C | |
| 13 | g.32338542A>G | CA019687 | BRCA2 | c.4187A>G (p.Gln1396Arg) c.3818A>G (p.Gln1273Arg) n.4187A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338542A>T | CA387780149 | BRCA2 | c.4187A>T (p.Gln1396Leu) c.3818A>T (p.Gln1273Leu) n.4187A>T | dbSNP gnomAD v4 |
| 13 | g.32338543del | CA019693 | BRCA2 | c.4188del (p.Glu1397LysfsTer13) c.3819del (p.Glu1274LysfsTer13) n.4188del | ClinVar dbSNP |
| 13 | g.32338543A= | CA2082809256 | BRCA2 | c.4188A= (p.Gln1396=) c.3819A= (p.Gln1273=) n.4188A= | |
| 13 | g.32338543A>C | CA387780153 | BRCA2 | c.4188A>C (p.Gln1396His) c.3819A>C (p.Gln1273His) n.4188A>C | |
| 13 | g.32338543A>G | CA483437899 | BRCA2 | c.4188A>G (p.Gln1396=) c.3819A>G (p.Gln1273=) n.4188A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338543A>T | CA387780156 | BRCA2 | c.4188A>T (p.Gln1396His) c.3819A>T (p.Gln1273His) n.4188A>T | |
| 13 | g.32338544G>A | CA019698 | BRCA2 | c.4189G>A (p.Glu1397Lys) c.3820G>A (p.Glu1274Lys) n.4189G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338544G>C | CA387780160 | BRCA2 | c.4189G>C (p.Glu1397Gln) c.3820G>C (p.Glu1274Gln) n.4189G>C | ClinVar dbSNP |
| 13 | g.32338544G= | CA2082809262 | BRCA2 | c.4189G= (p.Glu1397=) c.3820G= (p.Glu1274=) n.4189G= | |
| 13 | g.32338544G>T | CA387780162 | BRCA2 | c.4189G>T (p.Glu1397Ter) c.3820G>T (p.Glu1274Ter) n.4189G>T | dbSNP |
| 13 | g.32338545A= | CA2082809269 | BRCA2 | c.4190A= (p.Glu1397=) c.3821A= (p.Glu1274=) n.4190A= | |
| 13 | g.32338545A>C | CA387780164 | BRCA2 | c.4190A>C (p.Glu1397Ala) c.3821A>C (p.Glu1274Ala) n.4190A>C | ClinVar dbSNP |
| 13 | g.32338545A>G | CA387780168 | BRCA2 | c.4190A>G (p.Glu1397Gly) c.3821A>G (p.Glu1274Gly) n.4190A>G | |
| 13 | g.32338545A>T | CA387780166 | BRCA2 | c.4190A>T (p.Glu1397Val) c.3821A>T (p.Glu1274Val) n.4190A>T | dbSNP |
| 13 | g.32338546A>C | CA387780169 | BRCA2 | c.4191A>C (p.Glu1397Asp) c.3822A>C (p.Glu1274Asp) n.4191A>C | |
| 13 | g.32338546A>G | CA483437902 | BRCA2 | c.4191A>G (p.Glu1397=) c.3822A>G (p.Glu1274=) n.4191A>G | |
| 13 | g.32338546A>T | CA387780171 | BRCA2 | c.4191A>T (p.Glu1397Asp) c.3822A>T (p.Glu1274Asp) n.4191A>T | dbSNP |
| 13 | g.32338547G>A | CA10579603 | BRCA2 | c.4192G>A (p.Ala1398Thr) c.3823G>A (p.Ala1275Thr) n.4192G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338547G>C | CA387780173 | BRCA2 | c.4192G>C (p.Ala1398Pro) c.3823G>C (p.Ala1275Pro) n.4192G>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338547G= | CA2082809276 | BRCA2 | c.4192G= (p.Ala1398=) c.3823G= (p.Ala1275=) n.4192G= | |
| 13 | g.32338547G>T | CA387780175 | BRCA2 | c.4192G>T (p.Ala1398Ser) c.3823G>T (p.Ala1275Ser) n.4192G>T | |
| 13 | g.32338548C>A | CA387780177 | BRCA2 | c.4193C>A (p.Ala1398Glu) c.3824C>A (p.Ala1275Glu) n.4193C>A | dbSNP gnomAD v4 |
| 13 | g.32338548C= | CA2082809284 | BRCA2 | c.4193C= (p.Ala1398=) c.3824C= (p.Ala1275=) n.4193C= | |
| 13 | g.32338548C>G | CA387780179 | BRCA2 | c.4193C>G (p.Ala1398Gly) c.3824C>G (p.Ala1275Gly) n.4193C>G | dbSNP |
| 13 | g.32338548C>T | CA387780180 | BRCA2 | c.4193C>T (p.Ala1398Val) c.3824C>T (p.Ala1275Val) n.4193C>T | ClinVar dbSNP |
| 13 | g.32338549A= | CA2082809289 | BRCA2 | c.4194A= (p.Ala1398=) c.3825A= (p.Ala1275=) n.4194A= | |
| 13 | g.32338549A>C | CA483437905 | BRCA2 | c.4194A>C (p.Ala1398=) c.3825A>C (p.Ala1275=) n.4194A>C | |
| 13 | g.32338549A>G | CA483437907 | BRCA2 | c.4194A>G (p.Ala1398=) c.3825A>G (p.Ala1275=) n.4194A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338549A>T | CA483437906 | BRCA2 | c.4194A>T (p.Ala1398=) c.3825A>T (p.Ala1275=) n.4194A>T | dbSNP |
| 13 | g.32338550T>A | CA387780181 | BRCA2 | c.4195T>A (p.Cys1399Ser) c.3826T>A (p.Cys1276Ser) n.4195T>A | dbSNP |
| 13 | g.32338550T>C | CA019706 | BRCA2 | c.4195T>C (p.Cys1399Arg) c.3826T>C (p.Cys1276Arg) n.4195T>C | ClinVar dbSNP |
| 13 | g.32338550T>G | CA387780185 | BRCA2 | c.4195T>G (p.Cys1399Gly) c.3826T>G (p.Cys1276Gly) n.4195T>G | |
| 13 | g.32338550T= | CA2082809295 | BRCA2 | c.4195T= (p.Cys1399=) c.3826T= (p.Cys1276=) n.4195T= | |
| 13 | g.32338551G>A | CA387780190 | BRCA2 | c.4196G>A (p.Cys1399Tyr) c.3827G>A (p.Cys1276Tyr) n.4196G>A | dbSNP |
| 13 | g.32338551G>C | CA387780187 | BRCA2 | c.4196G>C (p.Cys1399Ser) c.3827G>C (p.Cys1276Ser) n.4196G>C | dbSNP |
| 13 | g.32338551G= | CA2082809302 | BRCA2 | c.4196G= (p.Cys1399=) c.3827G= (p.Cys1276=) n.4196G= | |
| 13 | g.32338551G>T | CA6940759 | BRCA2 | c.4196G>T (p.Cys1399Phe) c.3827G>T (p.Cys1276Phe) n.4196G>T | ClinVar dbSNP ExAC gnomAD v2 |
| 13 | g.32338552T>A | CA387780191 | BRCA2 | c.4197T>A (p.Cys1399Ter) c.3828T>A (p.Cys1276Ter) n.4197T>A | ClinVar dbSNP |
| 13 | g.32338552T>C | CA483437909 | BRCA2 | c.4197T>C (p.Cys1399=) c.3828T>C (p.Cys1276=) n.4197T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338552T>G | CA387780193 | BRCA2 | c.4197T>G (p.Cys1399Trp) c.3828T>G (p.Cys1276Trp) n.4197T>G | dbSNP |
| 13 | g.32338552T= | CA2082809309 | BRCA2 | c.4197T= (p.Cys1399=) c.3828T= (p.Cys1276=) n.4197T= | |
| 13 | g.32338553C>A | CA387780195 | BRCA2 | c.4198C>A (p.His1400Asn) c.3829C>A (p.His1277Asn) n.4198C>A | dbSNP |
| 13 | g.32338553C= | CA2082809314 | BRCA2 | c.4198C= (p.His1400=) c.3829C= (p.His1277=) n.4198C= | |
| 13 | g.32338553C>G | CA387780197 | BRCA2 | c.4198C>G (p.His1400Asp) c.3829C>G (p.His1277Asp) n.4198C>G | dbSNP |
| 13 | g.32338553C>T | CA387780199 | BRCA2 | c.4198C>T (p.His1400Tyr) c.3829C>T (p.His1277Tyr) n.4198C>T | ClinVar dbSNP |
| 13 | g.32338554A= | CA2082809318 | BRCA2 | c.4199A= (p.His1400=) c.3830A= (p.His1277=) n.4199A= | |
| 13 | g.32338554A>C | CA387780201 | BRCA2 | c.4199A>C (p.His1400Pro) c.3830A>C (p.His1277Pro) n.4199A>C | |
| 13 | g.32338554A>G | CA387780202 | BRCA2 | c.4199A>G (p.His1400Arg) c.3830A>G (p.His1277Arg) n.4199A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338554A>T | CA387780207 | BRCA2 | c.4199A>T (p.His1400Leu) c.3830A>T (p.His1277Leu) n.4199A>T | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338555T>A | CA387780209 | BRCA2 | c.4200T>A (p.His1400Gln) c.3831T>A (p.His1277Gln) n.4200T>A | dbSNP |
| 13 | g.32338555T>C | CA483437913 | BRCA2 | c.4200T>C (p.His1400=) c.3831T>C (p.His1277=) n.4200T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338555T>G | CA387780211 | BRCA2 | c.4200T>G (p.His1400Gln) c.3831T>G (p.His1277Gln) n.4200T>G | dbSNP |
| 13 | g.32338555T= | CA2082809324 | BRCA2 | c.4200T= (p.His1400=) c.3831T= (p.His1277=) n.4200T= | |
| 13 | g.32338556G>A | CA387780213 | BRCA2 | c.4201G>A (p.Gly1401Ser) c.3832G>A (p.Gly1278Ser) n.4201G>A | ClinVar dbSNP |
| 13 | g.32338556G>C | CA387780215 | BRCA2 | c.4201G>C (p.Gly1401Arg) c.3832G>C (p.Gly1278Arg) n.4201G>C | dbSNP |
| 13 | g.32338556G= | CA2082809353 | BRCA2 | c.4201G= (p.Gly1401=) c.3832G= (p.Gly1278=) n.4201G= | |
| 13 | g.32338556G>T | CA387780216 | BRCA2 | c.4201G>T (p.Gly1401Cys) c.3832G>T (p.Gly1278Cys) n.4201G>T | dbSNP gnomAD v4 |
| 13 | g.32338557G>A | CA387780220 | BRCA2 | c.4202G>A (p.Gly1401Asp) c.3833G>A (p.Gly1278Asp) n.4202G>A | dbSNP |
| 13 | g.32338557G>C | CA019711 | BRCA2 | c.4202G>C (p.Gly1401Ala) c.3833G>C (p.Gly1278Ala) n.4202G>C | ClinVar dbSNP |
| 13 | g.32338557G= | CA2082809359 | BRCA2 | c.4202G= (p.Gly1401=) c.3833G= (p.Gly1278=) n.4202G= | |
| 13 | g.32338557G>T | CA387780218 | BRCA2 | c.4202G>T (p.Gly1401Val) c.3833G>T (p.Gly1278Val) n.4202G>T | dbSNP |
| 13 | g.32338558T>A | CA483437915 | BRCA2 | c.4203T>A (p.Gly1401=) c.3834T>A (p.Gly1278=) n.4203T>A | |
| 13 | g.32338558T>C | CA483437916 | BRCA2 | c.4203T>C (p.Gly1401=) c.3834T>C (p.Gly1278=) n.4203T>C | ClinVar dbSNP |
| 13 | g.32338558T>G | CA483437917 | BRCA2 | c.4203T>G (p.Gly1401=) c.3834T>G (p.Gly1278=) n.4203T>G | ClinVar |
| 13 | g.32338560_32338562dup | CA2622601020 | BRCA2 | c.4205_4207dup (p.Asn1402_Thr1403insAsn) c.3836_3838dup (p.Asn1279_Thr1280insAsn) n.4205_4207dup | gnomAD v4 |
| 13 | g.32338559A= | CA2082809368 | BRCA2 | c.4204A= (p.Asn1402=) c.3835A= (p.Asn1279=) n.4204A= | |
| 13 | g.32338559A>C | CA019715 | BRCA2 | c.4204A>C (p.Asn1402His) c.3835A>C (p.Asn1279His) n.4204A>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338559A>G | CA387780223 | BRCA2 | c.4204A>G (p.Asn1402Asp) c.3835A>G (p.Asn1279Asp) n.4204A>G | dbSNP |
| 13 | g.32338559A>T | CA387780225 | BRCA2 | c.4204A>T (p.Asn1402Tyr) c.3835A>T (p.Asn1279Tyr) n.4204A>T | dbSNP |
| 13 | g.32338560A>C | CA387780227 | BRCA2 | c.4205A>C (p.Asn1402Thr) c.3836A>C (p.Asn1279Thr) n.4205A>C | |
| 13 | g.32338560A>G | CA387780230 | BRCA2 | c.4205A>G (p.Asn1402Ser) c.3836A>G (p.Asn1279Ser) n.4205A>G | ClinVar dbSNP |
| 13 | g.32338560A>T | CA387780233 | BRCA2 | c.4205A>T (p.Asn1402Ile) c.3836A>T (p.Asn1279Ile) n.4205A>T | dbSNP |
| 13 | g.32338561T>A | CA387780235 | BRCA2 | c.4206T>A (p.Asn1402Lys) c.3837T>A (p.Asn1279Lys) n.4206T>A | dbSNP |
| 13 | g.32338561T>C | CA10583101 | BRCA2 | c.4206T>C (p.Asn1402=) c.3837T>C (p.Asn1279=) n.4206T>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338561T>G | CA387780238 | BRCA2 | c.4206T>G (p.Asn1402Lys) c.3837T>G (p.Asn1279Lys) n.4206T>G | dbSNP |
| 13 | g.32338561T= | CA2082809375 | BRCA2 | c.4206T= (p.Asn1402=) c.3837T= (p.Asn1279=) n.4206T= | |
| 13 | g.32338562_32338564del | CA2499222157 | BRCA2 | c.4207_4209del (p.Thr1403del) c.3838_3840del (p.Thr1280del) n.4207_4209del | ClinVar dbSNP |
| 13 | g.32338562A= | CA2082809382 | BRCA2 | c.4207A= (p.Thr1403=) c.3838A= (p.Thr1280=) n.4207A= | |
| 13 | g.32338562A>C | CA387780240 | BRCA2 | c.4207A>C (p.Thr1403Pro) c.3838A>C (p.Thr1280Pro) n.4207A>C | dbSNP |
| 13 | g.32338562A>G | CA387780242 | BRCA2 | c.4207A>G (p.Thr1403Ala) c.3838A>G (p.Thr1280Ala) n.4207A>G | ClinVar dbSNP |
| 13 | g.32338562A>T | CA387780244 | BRCA2 | c.4207A>T (p.Thr1403Ser) c.3838A>T (p.Thr1280Ser) n.4207A>T | dbSNP |
| 13 | g.32338562dup | CA2499222158 | BRCA2 | c.4207dup (p.Thr1403AsnfsTer4) c.3838dup (p.Thr1280AsnfsTer4) n.4207dup | |
| 13 | g.32338562_32338565delinsACTT | CA2082809385 | BRCA2 | c.4207_4210delinsACTT (p.Thr1403=) c.3838_3841delinsACTT (p.Thr1280=) n.4207_4210delinsACTT | |
| 13 | g.32338563_32338567del | CA2499222159 | BRCA2 | c.4208_4212del (p.Thr1403LysfsTer2) c.3839_3843del (p.Thr1280LysfsTer2) n.4208_4212del | ClinVar dbSNP |
| 13 | g.32338563C>A | CA387780246 | BRCA2 | c.4208C>A (p.Thr1403Asn) c.3839C>A (p.Thr1280Asn) n.4208C>A | dbSNP |
| 13 | g.32338563C= | CA2082809403 | BRCA2 | c.4208C= (p.Thr1403=) c.3839C= (p.Thr1280=) n.4208C= | |
| 13 | g.32338563C>G | CA387780250 | BRCA2 | c.4208C>G (p.Thr1403Ser) c.3839C>G (p.Thr1280Ser) n.4208C>G | ClinVar dbSNP COSMIC COSMIC |
| 13 | g.32338563C>T | CA387780248 | BRCA2 | c.4208C>T (p.Thr1403Ile) c.3839C>T (p.Thr1280Ile) n.4208C>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338564_32338566del | CA2082809396 | BRCA2 | c.4209_4211del (p.Ser1404del) c.3840_3842del (p.Ser1281del) n.4209_4211del | ClinVar dbSNP |
| 13 | g.32338564T>A | CA483437930 | BRCA2 | c.4209T>A (p.Thr1403=) c.3840T>A (p.Thr1280=) n.4209T>A | ClinVar dbSNP |
| 13 | g.32338564T>C | CA483437926 | BRCA2 | c.4209T>C (p.Thr1403=) c.3840T>C (p.Thr1280=) n.4209T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338564T>G | CA483437929 | BRCA2 | c.4209T>G (p.Thr1403=) c.3840T>G (p.Thr1280=) n.4209T>G | |
| 13 | g.32338564T= | CA2082809412 | BRCA2 | c.4209T= (p.Thr1403=) c.3840T= (p.Thr1280=) n.4209T= | |
| 13 | g.32338564_32338569delinsTTCAAA | CA2082809415 | BRCA2 | c.4209_4214delinsTTCAAA (p.Thr1403=) c.3840_3845delinsTTCAAA (p.Thr1280=) n.4209_4214delinsTTCAAA | |
| 13 | g.32338565T>A | CA387780252 | BRCA2 | c.4210T>A (p.Ser1404Thr) c.3841T>A (p.Ser1281Thr) n.4210T>A | dbSNP |
| 13 | g.32338565T>C | CA387780257 | BRCA2 | c.4210T>C (p.Ser1404Pro) c.3841T>C (p.Ser1281Pro) n.4210T>C | |
| 13 | g.32338565T>G | CA387780255 | BRCA2 | c.4210T>G (p.Ser1404Ala) c.3841T>G (p.Ser1281Ala) n.4210T>G | |
| 13 | g.32338565_32338566delinsTC | CA2082809420 | BRCA2 | c.4210_4211delinsTC (p.Ser1404=) c.3841_3842delinsTC (p.Ser1281=) n.4210_4211delinsTC | |
| 13 | g.32338566_32338570del | CA019721 | BRCA2 | c.4211_4215del (p.Ser1404Ter) c.3842_3846del (p.Ser1281Ter) n.4211_4215del | ClinVar dbSNP |
| 13 | g.32338566del | CA019731 | BRCA2 | c.4211del (p.Ser1404Ter) c.3842del (p.Ser1281Ter) n.4211del | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338566C>A | CA387780259 | BRCA2 | c.4211C>A (p.Ser1404Ter) c.3842C>A (p.Ser1281Ter) n.4211C>A | ClinVar dbSNP |
| 13 | g.32338566C= | CA2082809467 | BRCA2 | c.4211C= (p.Ser1404=) c.3842C= (p.Ser1281=) n.4211C= | |
| 13 | g.32338566C>G | CA10589245 | BRCA2 | c.4211C>G (p.Ser1404Ter) c.3842C>G (p.Ser1281Ter) n.4211C>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338566C>T | CA019726 | BRCA2 | c.4211C>T (p.Ser1404Leu) c.3842C>T (p.Ser1281Leu) n.4211C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338567A>C | CA483437934 | BRCA2 | c.4212A>C (p.Ser1404=) c.3843A>C (p.Ser1281=) n.4212A>C | ClinVar |
| 13 | g.32338567A>G | CA483437935 | BRCA2 | c.4212A>G (p.Ser1404=) c.3843A>G (p.Ser1281=) n.4212A>G | |
| 13 | g.32338567A>T | CA483437936 | BRCA2 | c.4212A>T (p.Ser1404=) c.3843A>T (p.Ser1281=) n.4212A>T | dbSNP |
| 13 | g.32338569_32338573del | CA2695199717 | BRCA2 | c.4214_4218del (p.Asn1405ArgfsTer7) c.3845_3849del (p.Asn1282ArgfsTer7) n.4214_4218del | ClinVar |
| 13 | g.32338568A= | CA2082809486 | BRCA2 | c.4213A= (p.Asn1405=) c.3844A= (p.Asn1282=) n.4213A= | |
| 13 | g.32338568A>C | CA387780266 | BRCA2 | c.4213A>C (p.Asn1405His) c.3844A>C (p.Asn1282His) n.4213A>C | ClinVar dbSNP |
| 13 | g.32338568A>G | CA387780264 | BRCA2 | c.4213A>G (p.Asn1405Asp) c.3844A>G (p.Asn1282Asp) n.4213A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338568A>T | CA387780268 | BRCA2 | c.4213A>T (p.Asn1405Tyr) c.3844A>T (p.Asn1282Tyr) n.4213A>T | dbSNP |
| 13 | g.32338569A>C | CA387780270 | BRCA2 | c.4214A>C (p.Asn1405Thr) c.3845A>C (p.Asn1282Thr) n.4214A>C | |
| 13 | g.32338569A>G | CA387780274 | BRCA2 | c.4214A>G (p.Asn1405Ser) c.3845A>G (p.Asn1282Ser) n.4214A>G | ClinVar dbSNP |
| 13 | g.32338569A>T | CA387780272 | BRCA2 | c.4214A>T (p.Asn1405Ile) c.3845A>T (p.Asn1282Ile) n.4214A>T | dbSNP |
| 13 | g.32338570T>A | CA387780275 | BRCA2 | c.4215T>A (p.Asn1405Lys) c.3846T>A (p.Asn1282Lys) n.4215T>A | ClinVar |
| 13 | g.32338570T>C | CA483437938 | BRCA2 | c.4215T>C (p.Asn1405=) c.3846T>C (p.Asn1282=) n.4215T>C | |
| 13 | g.32338570T>G | CA387780277 | BRCA2 | c.4215T>G (p.Asn1405Lys) c.3846T>G (p.Asn1282Lys) n.4215T>G | |
| 13 | g.32338570_32338573delinsTAAA | CA2082809497 | BRCA2 | c.4215_4218delinsTAAA (p.Asn1405=) c.3846_3849delinsTAAA (p.Asn1282=) n.4215_4218delinsTAAA | |
| 13 | g.32338570_32338574delinsTAAAG | CA2082809500 | BRCA2 | c.4215_4219delinsTAAAG (p.Asn1405=) c.3846_3850delinsTAAAG (p.Asn1282=) n.4215_4219delinsTAAAG | |
| 13 | g.32338571A= | CA2082809528 | BRCA2 | c.4216A= (p.Lys1406=) c.3847A= (p.Lys1283=) n.4216A= | |
| 13 | g.32338571A>C | CA387780278 | BRCA2 | c.4216A>C (p.Lys1406Gln) c.3847A>C (p.Lys1283Gln) n.4216A>C | |
| 13 | g.32338571A>G | CA10579604 | BRCA2 | c.4216A>G (p.Lys1406Glu) c.3847A>G (p.Lys1283Glu) n.4216A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338571A>T | CA387780281 | BRCA2 | c.4216A>T (p.Lys1406Ter) c.3847A>T (p.Lys1283Ter) n.4216A>T | dbSNP |
| 13 | g.32338571_32338573del | CA019735 | BRCA2 | c.4216_4218del (p.Lys1406del) c.3847_3849del (p.Lys1283del) n.4216_4218del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338573_32338576del | CA019739 | BRCA2 | c.4218_4221del (p.Lys1406AsnfsTer3) c.3849_3852del (p.Lys1283AsnfsTer3) n.4218_4221del | ClinVar dbSNP gnomAD v4 COSMIC |
| 13 | g.32338572A>C | CA387780285 | BRCA2 | c.4217A>C (p.Lys1406Thr) c.3848A>C (p.Lys1283Thr) n.4217A>C | |
| 13 | g.32338572A>G | CA387780287 | BRCA2 | c.4217A>G (p.Lys1406Arg) c.3848A>G (p.Lys1283Arg) n.4217A>G | |
| 13 | g.32338572A>T | CA387780288 | BRCA2 | c.4217A>T (p.Lys1406Ile) c.3848A>T (p.Lys1283Ile) n.4217A>T | dbSNP |
| 13 | g.32338573A= | CA2082809535 | BRCA2 | c.4218A= (p.Lys1406=) c.3849A= (p.Lys1283=) n.4218A= | |
| 13 | g.32338573A>C | CA387780291 | BRCA2 | c.4218A>C (p.Lys1406Asn) c.3849A>C (p.Lys1283Asn) n.4218A>C | ClinVar dbSNP |
| 13 | g.32338573A>G | CA483437942 | BRCA2 | c.4218A>G (p.Lys1406=) c.3849A>G (p.Lys1283=) n.4218A>G | ClinVar dbSNP |
| 13 | g.32338573A>T | CA387780292 | BRCA2 | c.4218A>T (p.Lys1406Asn) c.3849A>T (p.Lys1283Asn) n.4218A>T | dbSNP |
| 13 | g.32338574G>A | CA387780294 | BRCA2 | c.4219G>A (p.Glu1407Lys) c.3850G>A (p.Glu1284Lys) n.4219G>A | dbSNP |
| 13 | g.32338574G>C | CA387780298 | BRCA2 | c.4219G>C (p.Glu1407Gln) c.3850G>C (p.Glu1284Gln) n.4219G>C | dbSNP COSMIC COSMIC |
| 13 | g.32338574G>T | CA387780296 | BRCA2 | c.4219G>T (p.Glu1407Ter) c.3850G>T (p.Glu1284Ter) n.4219G>T | ClinVar dbSNP |
| 13 | g.32338574_32338575delinsGA | CA2082809546 | BRCA2 | c.4219_4220delinsGA (p.Glu1407=) c.3850_3851delinsGA (p.Glu1284=) n.4219_4220delinsGA | |
| 13 | g.32338575A= | CA2082809563 | BRCA2 | c.4220A= (p.Glu1407=) c.3851A= (p.Glu1284=) n.4220A= | |
| 13 | g.32338575A>C | CA387780300 | BRCA2 | c.4220A>C (p.Glu1407Ala) c.3851A>C (p.Glu1284Ala) n.4220A>C | |
| 13 | g.32338575A>G | CA387780302 | BRCA2 | c.4220A>G (p.Glu1407Gly) c.3851A>G (p.Glu1284Gly) n.4220A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338575A>T | CA387780304 | BRCA2 | c.4220A>T (p.Glu1407Val) c.3851A>T (p.Glu1284Val) n.4220A>T | ClinVar dbSNP |
| 13 | g.32338576del | CA10589246 | BRCA2 | c.4221del (p.Glu1407AspfsTer3) c.3852del (p.Glu1284AspfsTer3) n.4221del | ClinVar dbSNP |
| 13 | g.32338576A>C | CA387780307 | BRCA2 | c.4221A>C (p.Glu1407Asp) c.3852A>C (p.Glu1284Asp) n.4221A>C | dbSNP |
| 13 | g.32338576A>G | CA483437948 | BRCA2 | c.4221A>G (p.Glu1407=) c.3852A>G (p.Glu1284=) n.4221A>G | dbSNP |
| 13 | g.32338576A>T | CA387780309 | BRCA2 | c.4221A>T (p.Glu1407Asp) c.3852A>T (p.Glu1284Asp) n.4221A>T | dbSNP |
| 13 | g.32338577_32338578del | CA2580087261 | BRCA2 | c.4222_4223del (p.Gln1408ValfsTer5) c.3853_3854del (p.Gln1285ValfsTer5) n.4222_4223del | ClinVar |
| 13 | g.32338577C>A | CA387780311 | BRCA2 | c.4222C>A (p.Gln1408Lys) c.3853C>A (p.Gln1285Lys) n.4222C>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338577C= | CA2082809588 | BRCA2 | c.4222C= (p.Gln1408=) c.3853C= (p.Gln1285=) n.4222C= | |
| 13 | g.32338577C>G | CA387780313 | BRCA2 | c.4222C>G (p.Gln1408Glu) c.3853C>G (p.Gln1285Glu) n.4222C>G | dbSNP gnomAD v4 |
| 13 | g.32338577C>T | CA019744 | BRCA2 | c.4222C>T (p.Gln1408Ter) c.3853C>T (p.Gln1285Ter) n.4222C>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338577dup | CA2573149372 | BRCA2 | c.4222dup (p.Gln1408ProfsTer6) c.3853dup (p.Gln1285ProfsTer6) n.4222dup | ClinVar dbSNP |
| 13 | g.32338577_32338578delinsCA | CA2082809581 | BRCA2 | c.4222_4223delinsCA (p.Gln1408=) c.3853_3854delinsCA (p.Gln1285=) n.4222_4223delinsCA | |
| 13 | g.32338577_32338581delinsCAGTT | CA2082809578 | BRCA2 | c.4222_4226delinsCAGTT (p.Gln1408=) c.3853_3857delinsCAGTT (p.Gln1285=) n.4222_4226delinsCAGTT | |
| 13 | g.32338578del | CA019749 | BRCA2 | c.4223del (p.Gln1408ArgfsTer2) c.3854del (p.Gln1285ArgfsTer2) n.4223del | ClinVar dbSNP |
| 13 | g.32338578A= | CA2082809603 | BRCA2 | c.4223A= (p.Gln1408=) c.3854A= (p.Gln1285=) n.4223A= | |
| 13 | g.32338578A>C | CA387780320 | BRCA2 | c.4223A>C (p.Gln1408Pro) c.3854A>C (p.Gln1285Pro) n.4223A>C | |
| 13 | g.32338578A>G | CA6940760 | BRCA2 | c.4223A>G (p.Gln1408Arg) c.3854A>G (p.Gln1285Arg) n.4223A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338578A>T | CA387780318 | BRCA2 | c.4223A>T (p.Gln1408Leu) c.3854A>T (p.Gln1285Leu) n.4223A>T | dbSNP |
| 13 | g.32338579_32338582del | CA954694064 | BRCA2 | c.4224_4227del (p.Thr1410LeufsTer8) c.3855_3858del (p.Thr1287LeufsTer8) n.4224_4227del | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338579G>A | CA337867 | BRCA2 | c.4224G>A (p.Gln1408=) c.3855G>A (p.Gln1285=) n.4224G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338579G>C | CA387780322 | BRCA2 | c.4224G>C (p.Gln1408His) c.3855G>C (p.Gln1285His) n.4224G>C | |
| 13 | g.32338579G= | CA2082809612 | BRCA2 | c.4224G= (p.Gln1408=) c.3855G= (p.Gln1285=) n.4224G= | |
| 13 | g.32338579G>T | CA387780324 | BRCA2 | c.4224G>T (p.Gln1408His) c.3855G>T (p.Gln1285His) n.4224G>T | |
| 13 | g.32338580T>A | CA387780326 | BRCA2 | c.4225T>A (p.Leu1409Ile) c.3856T>A (p.Leu1286Ile) n.4225T>A | dbSNP |
| 13 | g.32338580T>C | CA483437957 | BRCA2 | c.4225T>C (p.Leu1409=) c.3856T>C (p.Leu1286=) n.4225T>C | dbSNP |
| 13 | g.32338580T>G | CA387780328 | BRCA2 | c.4225T>G (p.Leu1409Val) c.3856T>G (p.Leu1286Val) n.4225T>G | ClinVar dbSNP |
| 13 | g.32338580T= | CA2082809628 | BRCA2 | c.4225T= (p.Leu1409=) c.3856T= (p.Leu1286=) n.4225T= | |
| 13 | g.32338581T>A | CA16606423 | BRCA2 | c.4226T>A (p.Leu1409Ter) c.3857T>A (p.Leu1286Ter) n.4226T>A | ClinVar dbSNP |
| 13 | g.32338581T>C | CA387780330 | BRCA2 | c.4226T>C (p.Leu1409Ser) c.3857T>C (p.Leu1286Ser) n.4226T>C | gnomAD v4 |
| 13 | g.32338581T>G | CA387780332 | BRCA2 | c.4226T>G (p.Leu1409Ter) c.3857T>G (p.Leu1286Ter) n.4226T>G | |
| 13 | g.32338581T= | CA2082809640 | BRCA2 | c.4226T= (p.Leu1409=) c.3857T= (p.Leu1286=) n.4226T= | |
| 13 | g.32338582A>C | CA387780335 | BRCA2 | c.4227A>C (p.Leu1409Phe) c.3858A>C (p.Leu1286Phe) n.4227A>C | |
| 13 | g.32338582A>G | CA483437958 | BRCA2 | c.4227A>G (p.Leu1409=) c.3858A>G (p.Leu1286=) n.4227A>G | |
| 13 | g.32338582A>T | CA387780336 | BRCA2 | c.4227A>T (p.Leu1409Phe) c.3858A>T (p.Leu1286Phe) n.4227A>T | dbSNP |
| 13 | g.32338583dup | CA10586066 | BRCA2 | c.4228dup (p.Thr1410AsnfsTer4) c.3859dup (p.Thr1287AsnfsTer4) n.4228dup | ClinVar dbSNP |
| 13 | g.32338582_32338583dup | CA2697551729 | BRCA2 | c.4227_4228dup (p.Thr1410LysfsTer10) c.3858_3859dup (p.Thr1287LysfsTer10) n.4227_4228dup | ClinVar |
| 13 | g.32338583A>C | CA387780342 | BRCA2 | c.4228A>C (p.Thr1410Pro) c.3859A>C (p.Thr1287Pro) n.4228A>C | dbSNP |
| 13 | g.32338583A>G | CA387780341 | BRCA2 | c.4228A>G (p.Thr1410Ala) c.3859A>G (p.Thr1287Ala) n.4228A>G | dbSNP |
| 13 | g.32338583A>T | CA387780339 | BRCA2 | c.4228A>T (p.Thr1410Ser) c.3859A>T (p.Thr1287Ser) n.4228A>T | ClinVar dbSNP |
| 13 | g.32338584C>A | CA387780344 | BRCA2 | c.4229C>A (p.Thr1410Asn) c.3860C>A (p.Thr1287Asn) n.4229C>A | ClinVar dbSNP |
| 13 | g.32338584C= | CA2082809658 | BRCA2 | c.4229C= (p.Thr1410=) c.3860C= (p.Thr1287=) n.4229C= | |
| 13 | g.32338584C>G | CA387780346 | BRCA2 | c.4229C>G (p.Thr1410Ser) c.3860C>G (p.Thr1287Ser) n.4229C>G | dbSNP |
| 13 | g.32338584C>T | CA387780348 | BRCA2 | c.4229C>T (p.Thr1410Ile) c.3860C>T (p.Thr1287Ile) n.4229C>T | dbSNP |
| 13 | g.32338584dup | CA2739291771 | BRCA2 | c.4229dup (p.Ala1411CysfsTer3) c.3860dup (p.Ala1288CysfsTer3) n.4229dup | |
| 13 | g.32338584_32338585insA | CA10589247 | BRCA2 | c.4229_4230insA (p.Ala1411CysfsTer3) c.3860_3861insA (p.Ala1288CysfsTer3) n.4229_4230insA | ClinVar dbSNP |
| 13 | g.32338585T>A | CA483437960 | BRCA2 | c.4230T>A (p.Thr1410=) c.3861T>A (p.Thr1287=) n.4230T>A | dbSNP |
| 13 | g.32338585T>C | CA483437961 | BRCA2 | c.4230T>C (p.Thr1410=) c.3861T>C (p.Thr1287=) n.4230T>C | dbSNP |
| 13 | g.32338585T>G | CA483437962 | BRCA2 | c.4230T>G (p.Thr1410=) c.3861T>G (p.Thr1287=) n.4230T>G | ClinVar |
| 13 | g.32338586G>A | CA387780352 | BRCA2 | c.4231G>A (p.Ala1411Thr) c.3862G>A (p.Ala1288Thr) n.4231G>A | dbSNP |
| 13 | g.32338586G>C | CA387780353 | BRCA2 | c.4231G>C (p.Ala1411Pro) c.3862G>C (p.Ala1288Pro) n.4231G>C | dbSNP |
| 13 | g.32338586G= | CA2082809667 | BRCA2 | c.4231G= (p.Ala1411=) c.3862G= (p.Ala1288=) n.4231G= | |
| 13 | g.32338586G>T | CA387780355 | BRCA2 | c.4231G>T (p.Ala1411Ser) c.3862G>T (p.Ala1288Ser) n.4231G>T | ClinVar dbSNP gnomAD v2 |
| 13 | g.32338587C>A | CA387780356 | BRCA2 | c.4232C>A (p.Ala1411Asp) c.3863C>A (p.Ala1288Asp) n.4232C>A | dbSNP |
| 13 | g.32338587C= | CA2082809692 | BRCA2 | c.4232C= (p.Ala1411=) c.3863C= (p.Ala1288=) n.4232C= | |
| 13 | g.32338587C>G | CA019754 | BRCA2 | c.4232C>G (p.Ala1411Gly) c.3863C>G (p.Ala1288Gly) n.4232C>G | ClinVar dbSNP |
| 13 | g.32338587C>T | CA387780359 | BRCA2 | c.4232C>T (p.Ala1411Val) c.3863C>T (p.Ala1288Val) n.4232C>T | dbSNP |
| 13 | g.32338588T>A | CA483437965 | BRCA2 | c.4233T>A (p.Ala1411=) c.3864T>A (p.Ala1288=) n.4233T>A | dbSNP |
| 13 | g.32338588T>C | CA483437966 | BRCA2 | c.4233T>C (p.Ala1411=) c.3864T>C (p.Ala1288=) n.4233T>C | ClinVar dbSNP |
| 13 | g.32338588T>G | CA483437969 | BRCA2 | c.4233T>G (p.Ala1411=) c.3864T>G (p.Ala1288=) n.4233T>G | |
| 13 | g.32338588T= | CA2082809703 | BRCA2 | c.4233T= (p.Ala1411=) c.3864T= (p.Ala1288=) n.4233T= | |
| 13 | g.32338589A= | CA2082809716 | BRCA2 | c.4234A= (p.Thr1412=) c.3865A= (p.Thr1289=) n.4234A= | |
| 13 | g.32338589A>C | CA387780361 | BRCA2 | c.4234A>C (p.Thr1412Pro) c.3865A>C (p.Thr1289Pro) n.4234A>C | ClinVar dbSNP |
| 13 | g.32338589A>G | CA387780363 | BRCA2 | c.4234A>G (p.Thr1412Ala) c.3865A>G (p.Thr1289Ala) n.4234A>G | dbSNP |
| 13 | g.32338589A>T | CA387780365 | BRCA2 | c.4234A>T (p.Thr1412Ser) c.3865A>T (p.Thr1289Ser) n.4234A>T | dbSNP |
| 13 | g.32338589_32338591delinsC | CA2831039687 | BRCA2 | c.4234_4236delinsC (p.Thr1412GlnfsTer10) c.3865_3867delinsC (p.Thr1289GlnfsTer10) n.4234_4236delinsC | |
| 13 | g.32338590C>A | CA387780369 | BRCA2 | c.4235C>A (p.Thr1412Asn) c.3866C>A (p.Thr1289Asn) n.4235C>A | dbSNP |
| 13 | g.32338590C>G | CA387780371 | BRCA2 | c.4235C>G (p.Thr1412Ser) c.3866C>G (p.Thr1289Ser) n.4235C>G | dbSNP |
| 13 | g.32338590C>T | CA387780367 | BRCA2 | c.4235C>T (p.Thr1412Ile) c.3866C>T (p.Thr1289Ile) n.4235C>T | dbSNP |
| 13 | g.32338591T>A | CA483437970 | BRCA2 | c.4236T>A (p.Thr1412=) c.3867T>A (p.Thr1289=) n.4236T>A | |
| 13 | g.32338591T>C | CA483437971 | BRCA2 | c.4236T>C (p.Thr1412=) c.3867T>C (p.Thr1289=) n.4236T>C | |
| 13 | g.32338591T>G | CA483437972 | BRCA2 | c.4236T>G (p.Thr1412=) c.3867T>G (p.Thr1289=) n.4236T>G | |
| 13 | g.32338591_32338592delinsTA | CA2082809717 | BRCA2 | c.4236_4237delinsTA (p.Thr1412=) c.3867_3868delinsTA (p.Thr1289=) n.4236_4237delinsTA | |
| 13 | g.32338592A= | CA2082809724 | BRCA2 | c.4237A= (p.Lys1413=) c.3868A= (p.Lys1290=) n.4237A= | |
| 13 | g.32338592A>C | CA387780375 | BRCA2 | c.4237A>C (p.Lys1413Gln) c.3868A>C (p.Lys1290Gln) n.4237A>C | |
| 13 | g.32338592A>G | CA10577470 | BRCA2 | c.4237A>G (p.Lys1413Glu) c.3868A>G (p.Lys1290Glu) n.4237A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338592A>T | CA387780374 | BRCA2 | c.4237A>T (p.Lys1413Ter) c.3868A>T (p.Lys1290Ter) n.4237A>T | |
| 13 | g.32338595del | CA919242550 | BRCA2 | c.4240del (p.Thr1414ArgfsTer5) c.3871del (p.Thr1291ArgfsTer5) n.4240del | dbSNP |
| 13 | g.32338593A>C | CA387780378 | BRCA2 | c.4238A>C (p.Lys1413Thr) c.3869A>C (p.Lys1290Thr) n.4238A>C | |
| 13 | g.32338593A>G | CA387780380 | BRCA2 | c.4238A>G (p.Lys1413Arg) c.3869A>G (p.Lys1290Arg) n.4238A>G | |
| 13 | g.32338593A>T | CA387780381 | BRCA2 | c.4238A>T (p.Lys1413Ile) c.3869A>T (p.Lys1290Ile) n.4238A>T | dbSNP |
| 13 | g.32338594A>C | CA387780385 | BRCA2 | c.4239A>C (p.Lys1413Asn) c.3870A>C (p.Lys1290Asn) n.4239A>C | dbSNP |
| 13 | g.32338594A>G | CA483437975 | BRCA2 | c.4239A>G (p.Lys1413=) c.3870A>G (p.Lys1290=) n.4239A>G | dbSNP |
| 13 | g.32338594A>T | CA387780386 | BRCA2 | c.4239A>T (p.Lys1413Asn) c.3870A>T (p.Lys1290Asn) n.4239A>T | dbSNP |
| 13 | g.32338595A= | CA2082809733 | BRCA2 | c.4240A= (p.Thr1414=) c.3871A= (p.Thr1291=) n.4240A= | |
| 13 | g.32338595A>C | CA387780388 | BRCA2 | c.4240A>C (p.Thr1414Pro) c.3871A>C (p.Thr1291Pro) n.4240A>C | dbSNP |
| 13 | g.32338595A>G | CA10583102 | BRCA2 | c.4240A>G (p.Thr1414Ala) c.3871A>G (p.Thr1291Ala) n.4240A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338595A>T | CA387780390 | BRCA2 | c.4240A>T (p.Thr1414Ser) c.3871A>T (p.Thr1291Ser) n.4240A>T | dbSNP |
| 13 | g.32338596C>A | CA387780394 | BRCA2 | c.4241C>A (p.Thr1414Lys) c.3872C>A (p.Thr1291Lys) n.4241C>A | dbSNP |
| 13 | g.32338596C= | CA2082809753 | BRCA2 | c.4241C= (p.Thr1414=) c.3872C= (p.Thr1291=) n.4241C= | |
| 13 | g.32338596C>G | CA387780392 | BRCA2 | c.4241C>G (p.Thr1414Arg) c.3872C>G (p.Thr1291Arg) n.4241C>G | |
| 13 | g.32338596C>T | CA019759 | BRCA2 | c.4241C>T (p.Thr1414Met) c.3872C>T (p.Thr1291Met) n.4241C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338597G>A | CA10579605 | BRCA2 | c.4242G>A (p.Thr1414=) c.3873G>A (p.Thr1291=) n.4242G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338597G>C | CA483437979 | BRCA2 | c.4242G>C (p.Thr1414=) c.3873G>C (p.Thr1291=) n.4242G>C | dbSNP |
| 13 | g.32338597G= | CA2082809764 | BRCA2 | c.4242G= (p.Thr1414=) c.3873G= (p.Thr1291=) n.4242G= | |
| 13 | g.32338597G>T | CA019766 | BRCA2 | c.4242G>T (p.Thr1414=) c.3873G>T (p.Thr1291=) n.4242G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338598G>A | CA6940761 | BRCA2 | c.4243G>A (p.Glu1415Lys) c.3874G>A (p.Glu1292Lys) n.4243G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338598G>C | CA387780398 | BRCA2 | c.4243G>C (p.Glu1415Gln) c.3874G>C (p.Glu1292Gln) n.4243G>C | ClinVar dbSNP |
| 13 | g.32338598G= | CA2082809776 | BRCA2 | c.4243G= (p.Glu1415=) c.3874G= (p.Glu1292=) n.4243G= | |
| 13 | g.32338598G>T | CA019770 | BRCA2 | c.4243G>T (p.Glu1415Ter) c.3874G>T (p.Glu1292Ter) n.4243G>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338599A= | CA2082809788 | BRCA2 | c.4244A= (p.Glu1415=) c.3875A= (p.Glu1292=) n.4244A= | |
| 13 | g.32338599A>C | CA387780401 | BRCA2 | c.4244A>C (p.Glu1415Ala) c.3875A>C (p.Glu1292Ala) n.4244A>C | |
| 13 | g.32338599A>G | CA16613961 | BRCA2 | c.4244A>G (p.Glu1415Gly) c.3875A>G (p.Glu1292Gly) n.4244A>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338599A>T | CA387780403 | BRCA2 | c.4244A>T (p.Glu1415Val) c.3875A>T (p.Glu1292Val) n.4244A>T | |
| 13 | g.32338599_32338600delinsAG | CA2082809782 | BRCA2 | c.4244_4245delinsAG (p.Glu1415=) c.3875_3876delinsAG (p.Glu1292=) n.4244_4245delinsAG | |
| 13 | g.32338600del | CA6940762 | BRCA2 | c.4245del (p.Glu1415AspfsTer4) c.3876del (p.Glu1292AspfsTer4) n.4245del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338600G>A | CA019776 | BRCA2 | c.4245G>A (p.Glu1415=) c.3876G>A (p.Glu1292=) n.4245G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
| 13 | g.32338600G>C | CA387780407 | BRCA2 | c.4245G>C (p.Glu1415Asp) c.3876G>C (p.Glu1292Asp) n.4245G>C | dbSNP gnomAD v4 |
| 13 | g.32338600G= | CA2082809799 | BRCA2 | c.4245G= (p.Glu1415=) c.3876G= (p.Glu1292=) n.4245G= | |
| 13 | g.32338600G>T | CA387780409 | BRCA2 | c.4245G>T (p.Glu1415Asp) c.3876G>T (p.Glu1292Asp) n.4245G>T | dbSNP |
| 13 | g.32338601C>A | CA387780413 | BRCA2 | c.4246C>A (p.Gln1416Lys) c.3877C>A (p.Gln1293Lys) n.4246C>A | dbSNP gnomAD v4 |
| 13 | g.32338601C= | CA2082809826 | BRCA2 | c.4246C= (p.Gln1416=) c.3877C= (p.Gln1293=) n.4246C= | |
| 13 | g.32338601C>G | CA387780415 | BRCA2 | c.4246C>G (p.Gln1416Glu) c.3877C>G (p.Gln1293Glu) n.4246C>G | dbSNP |
| 13 | g.32338601C>T | CA019781 | BRCA2 | c.4246C>T (p.Gln1416Ter) c.3877C>T (p.Gln1293Ter) n.4246C>T | ClinVar dbSNP |
| 13 | g.32338601_32338602delinsCA | CA2082809822 | BRCA2 | c.4246_4247delinsCA (p.Gln1416=) c.3877_3878delinsCA (p.Gln1293=) n.4246_4247delinsCA | |
| 13 | g.32338602A= | CA2082809839 | BRCA2 | c.4247A= (p.Gln1416=) c.3878A= (p.Gln1293=) n.4247A= | |
| 13 | g.32338602A>C | CA387780416 | BRCA2 | c.4247A>C (p.Gln1416Pro) c.3878A>C (p.Gln1293Pro) n.4247A>C | |
| 13 | g.32338602A>G | CA387780419 | BRCA2 | c.4247A>G (p.Gln1416Arg) c.3878A>G (p.Gln1293Arg) n.4247A>G | ClinVar dbSNP |
| 13 | g.32338602A>T | CA387780420 | BRCA2 | c.4247A>T (p.Gln1416Leu) c.3878A>T (p.Gln1293Leu) n.4247A>T | ClinVar |
| 13 | g.32338605dup | CA1139663192 | BRCA2 | c.4250dup (p.Asn1417LysfsTer6) c.3881dup (p.Asn1294LysfsTer6) n.4250dup | ClinVar dbSNP |
| 13 | g.32338605del | CA247507399 | BRCA2 | c.4250del (p.Asn1417IlefsTer2) c.3881del (p.Asn1294IlefsTer2) n.4250del | dbSNP |
| 13 | g.32338603A= | CA2082809846 | BRCA2 | c.4248A= (p.Gln1416=) c.3879A= (p.Gln1293=) n.4248A= | |
| 13 | g.32338603A>C | CA387780424 | BRCA2 | c.4248A>C (p.Gln1416His) c.3879A>C (p.Gln1293His) n.4248A>C | |
| 13 | g.32338603A>G | CA019784 | BRCA2 | c.4248A>G (p.Gln1416=) c.3879A>G (p.Gln1293=) n.4248A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338603A>T | CA387780426 | BRCA2 | c.4248A>T (p.Gln1416His) c.3879A>T (p.Gln1293His) n.4248A>T | dbSNP |
| 13 | g.32338604A>C | CA387780428 | BRCA2 | c.4249A>C (p.Asn1417His) c.3880A>C (p.Asn1294His) n.4249A>C | |
| 13 | g.32338604A>G | CA387780430 | BRCA2 | c.4249A>G (p.Asn1417Asp) c.3880A>G (p.Asn1294Asp) n.4249A>G | |
| 13 | g.32338604A>T | CA387780432 | BRCA2 | c.4249A>T (p.Asn1417Tyr) c.3880A>T (p.Asn1294Tyr) n.4249A>T | |
| 13 | g.32338605A>C | CA387780435 | BRCA2 | c.4250A>C (p.Asn1417Thr) c.3881A>C (p.Asn1294Thr) n.4250A>C | |
| 13 | g.32338605A>G | CA387780436 | BRCA2 | c.4250A>G (p.Asn1417Ser) c.3881A>G (p.Asn1294Ser) n.4250A>G | |
| 13 | g.32338605A>T | CA387780438 | BRCA2 | c.4250A>T (p.Asn1417Ile) c.3881A>T (p.Asn1294Ile) n.4250A>T | dbSNP |
| 13 | g.32338606T>A | CA387780442 | BRCA2 | c.4251T>A (p.Asn1417Lys) c.3882T>A (p.Asn1294Lys) n.4251T>A | dbSNP |
| 13 | g.32338606T>C | CA16606682 | BRCA2 | c.4251T>C (p.Asn1417=) c.3882T>C (p.Asn1294=) n.4251T>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338606T>G | CA387780440 | BRCA2 | c.4251T>G (p.Asn1417Lys) c.3882T>G (p.Asn1294Lys) n.4251T>G | |
| 13 | g.32338606T= | CA2082809853 | BRCA2 | c.4251T= (p.Asn1417=) c.3882T= (p.Asn1294=) n.4251T= | |
| 13 | g.32338606_32338610delinsTATAA | CA2082809852 | BRCA2 | c.4251_4255delinsTATAA (p.Asn1417=) c.3882_3886delinsTATAA (p.Asn1294=) n.4251_4255delinsTATAA | |
| 13 | g.32338607A= | CA2082809864 | BRCA2 | c.4252A= (p.Ile1418=) c.3883A= (p.Ile1295=) n.4252A= | |
| 13 | g.32338607A>C | CA6940763 | BRCA2 | c.4252A>C (p.Ile1418Leu) c.3883A>C (p.Ile1295Leu) n.4252A>C | dbSNP ExAC gnomAD v2 |
| 13 | g.32338607A>G | CA019793 | BRCA2 | c.4252A>G (p.Ile1418Val) c.3883A>G (p.Ile1295Val) n.4252A>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338607A>T | CA387780446 | BRCA2 | c.4252A>T (p.Ile1418Leu) c.3883A>T (p.Ile1295Leu) n.4252A>T | dbSNP |
| 13 | g.32338607_32338610delinsT | CA10586521 | BRCA2 | c.4252_4255delinsT (p.Ile1418Ter) c.3883_3886delinsT (p.Ile1295Ter) n.4252_4255delinsT | ClinVar dbSNP |
| 13 | g.32338608del | CA2580087267 | BRCA2 | c.4253del (p.Ile1418LysfsTer30) c.3884del (p.Ile1295LysfsTer30) n.4253del | ClinVar |
| 13 | g.32338608T>A | CA387780449 | BRCA2 | c.4253T>A (p.Ile1418Lys) c.3884T>A (p.Ile1295Lys) n.4253T>A | |
| 13 | g.32338608T>C | CA6940764 | BRCA2 | c.4253T>C (p.Ile1418Thr) c.3884T>C (p.Ile1295Thr) n.4253T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338608T>G | CA387780451 | BRCA2 | c.4253T>G (p.Ile1418Arg) c.3884T>G (p.Ile1295Arg) n.4253T>G | |
| 13 | g.32338608T= | CA2082809892 | BRCA2 | c.4253T= (p.Ile1418=) c.3884T= (p.Ile1295=) n.4253T= | |
| 13 | g.32338608_32338610delinsTAA | CA2082809883 | BRCA2 | c.4253_4255delinsTAA (p.Ile1418=) c.3884_3886delinsTAA (p.Ile1295=) n.4253_4255delinsTAA | |
| 13 | g.32338609A= | CA2082809899 | BRCA2 | c.4254A= (p.Ile1418=) c.3885A= (p.Ile1295=) n.4254A= | |
| 13 | g.32338609A>C | CA483437995 | BRCA2 | c.4254A>C (p.Ile1418=) c.3885A>C (p.Ile1295=) n.4254A>C | |
| 13 | g.32338609A>G | CA16619702 | BRCA2 | c.4254A>G (p.Ile1418Met) c.3885A>G (p.Ile1295Met) n.4254A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338609A>T | CA483437996 | BRCA2 | c.4254A>T (p.Ile1418=) c.3885A>T (p.Ile1295=) n.4254A>T | dbSNP |
| 13 | g.32338612del | CA2573053810 | BRCA2 | c.4257del (p.Asp1420IlefsTer28) c.3888del (p.Asp1297IlefsTer28) n.4257del | ClinVar dbSNP |
| 13 | g.32338611_32338612del | CA609453787 | BRCA2 | c.4256_4257del (p.Lys1419ArgfsTer3) c.3887_3888del (p.Lys1296ArgfsTer3) n.4256_4257del | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338610A= | CA2082809906 | BRCA2 | c.4255A= (p.Lys1419=) c.3886A= (p.Lys1296=) n.4255A= | |
| 13 | g.32338610A>C | CA387780454 | BRCA2 | c.4255A>C (p.Lys1419Gln) c.3886A>C (p.Lys1296Gln) n.4255A>C | ClinVar dbSNP |
| 13 | g.32338610A>G | CA387780456 | BRCA2 | c.4255A>G (p.Lys1419Glu) c.3886A>G (p.Lys1296Glu) n.4255A>G | dbSNP |
| 13 | g.32338610A>T | CA387780457 | BRCA2 | c.4255A>T (p.Lys1419Ter) c.3886A>T (p.Lys1296Ter) n.4255A>T | dbSNP |
| 13 | g.32338611A= | CA2082809914 | BRCA2 | c.4256A= (p.Lys1419=) c.3887A= (p.Lys1296=) n.4256A= | |
| 13 | g.32338611A>C | CA387780460 | BRCA2 | c.4256A>C (p.Lys1419Thr) c.3887A>C (p.Lys1296Thr) n.4256A>C | ClinVar |
| 13 | g.32338611A>G | CA387780461 | BRCA2 | c.4256A>G (p.Lys1419Arg) c.3887A>G (p.Lys1296Arg) n.4256A>G | gnomAD v4 |
| 13 | g.32338611A>T | CA387780462 | BRCA2 | c.4256A>T (p.Lys1419Ile) c.3887A>T (p.Lys1296Ile) n.4256A>T | ClinVar dbSNP |
| 13 | g.32338612A>C | CA387780466 | BRCA2 | c.4257A>C (p.Lys1419Asn) c.3888A>C (p.Lys1296Asn) n.4257A>C | |
| 13 | g.32338612A>G | CA483437998 | BRCA2 | c.4257A>G (p.Lys1419=) c.3888A>G (p.Lys1296=) n.4257A>G | dbSNP |
| 13 | g.32338612A>T | CA387780464 | BRCA2 | c.4257A>T (p.Lys1419Asn) c.3888A>T (p.Lys1296Asn) n.4257A>T | dbSNP |
| 13 | g.32338612_32338613delinsAG | CA2082809917 | BRCA2 | c.4257_4258delinsAG (p.Lys1419=) c.3888_3889delinsAG (p.Lys1296=) n.4257_4258delinsAG | |
| 13 | g.32338613del | CA019805 | BRCA2 | c.4258del (p.Asp1420IlefsTer28) c.3889del (p.Asp1297IlefsTer28) n.4258del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338613G>A | CA387780469 | BRCA2 | c.4258G>A (p.Asp1420Asn) c.3889G>A (p.Asp1297Asn) n.4258G>A | dbSNP COSMIC COSMIC |
| 13 | g.32338613G>C | CA387780470 | BRCA2 | c.4258G>C (p.Asp1420His) c.3889G>C (p.Asp1297His) n.4258G>C | dbSNP |
| 13 | g.32338613G= | CA2082809925 | BRCA2 | c.4258G= (p.Asp1420=) c.3889G= (p.Asp1297=) n.4258G= | |
| 13 | g.32338613G>T | CA019810 | BRCA2 | c.4258G>T (p.Asp1420Tyr) c.3889G>T (p.Asp1297Tyr) n.4258G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338614A= | CA2082809933 | BRCA2 | c.4259A= (p.Asp1420=) c.3890A= (p.Asp1297=) n.4259A= | |
| 13 | g.32338614A>C | CA387780473 | BRCA2 | c.4259A>C (p.Asp1420Ala) c.3890A>C (p.Asp1297Ala) n.4259A>C | |
| 13 | g.32338614A>G | CA387780475 | BRCA2 | c.4259A>G (p.Asp1420Gly) c.3890A>G (p.Asp1297Gly) n.4259A>G | |
| 13 | g.32338614A>T | CA387780477 | BRCA2 | c.4259A>T (p.Asp1420Val) c.3890A>T (p.Asp1297Val) n.4259A>T | ClinVar dbSNP |
| 13 | g.32338614dup | CA2575387649 | BRCA2 | c.4259dup (p.Asp1420GlufsTer3) c.3890dup (p.Asp1297GlufsTer3) n.4259dup | |
| 13 | g.32338615T>A | CA387780481 | BRCA2 | c.4260T>A (p.Asp1420Glu) c.3891T>A (p.Asp1297Glu) n.4260T>A | dbSNP |
| 13 | g.32338615T>C | CA483438002 | BRCA2 | c.4260T>C (p.Asp1420=) c.3891T>C (p.Asp1297=) n.4260T>C | |
| 13 | g.32338615T>G | CA387780479 | BRCA2 | c.4260T>G (p.Asp1420Glu) c.3891T>G (p.Asp1297Glu) n.4260T>G | dbSNP |
| 13 | g.32338615delinsAA | CA2499222161 | BRCA2 | c.4260delinsAA (p.Asp1420GlufsTer3) c.3891delinsAA (p.Asp1297GlufsTer3) n.4260delinsAA | ClinVar dbSNP |
| 13 | g.32338618dup | CA16619703 | BRCA2 | c.4263dup (p.Glu1422Ter) c.3894dup (p.Glu1299Ter) n.4263dup | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338619_32338638del | CA2499222160 | BRCA2 | c.4264_4283del (p.Glu1422SerfsTer9) c.3895_3914del (p.Glu1299SerfsTer9) n.4264_4283del | |
| 13 | g.32338616T>A | CA387780484 | BRCA2 | c.4261T>A (p.Phe1421Ile) c.3892T>A (p.Phe1298Ile) n.4261T>A | dbSNP |
| 13 | g.32338616T>C | CA10583103 | BRCA2 | c.4261T>C (p.Phe1421Leu) c.3892T>C (p.Phe1298Leu) n.4261T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338616T>G | CA387780495 | BRCA2 | c.4261T>G (p.Phe1421Val) c.3892T>G (p.Phe1298Val) n.4261T>G | |
| 13 | g.32338616T= | CA2082809951 | BRCA2 | c.4261T= (p.Phe1421=) c.3892T= (p.Phe1298=) n.4261T= | |
| 13 | g.32338616_32338623delinsTTTGAGAC | CA2082809955 | BRCA2 | c.4261_4268delinsTTTGAGAC (p.Phe1421=) c.3892_3899delinsTTTGAGAC (p.Phe1298=) n.4261_4268delinsTTTGAGAC | |
| 13 | g.32338617T>A | CA387780496 | BRCA2 | c.4262T>A (p.Phe1421Tyr) c.3893T>A (p.Phe1298Tyr) n.4262T>A | dbSNP |
| 13 | g.32338617T>C | CA387780498 | BRCA2 | c.4262T>C (p.Phe1421Ser) c.3893T>C (p.Phe1298Ser) n.4262T>C | gnomAD v4 |
| 13 | g.32338617T>G | CA387780501 | BRCA2 | c.4262T>G (p.Phe1421Cys) c.3893T>G (p.Phe1298Cys) n.4262T>G | |
| 13 | g.32338619_32338625del | CA10589248 | BRCA2 | c.4264_4270del (p.Glu1422LeufsTer24) c.3895_3901del (p.Glu1299LeufsTer24) n.4264_4270del | ClinVar dbSNP |
| 13 | g.32338618T>A | CA387780504 | BRCA2 | c.4263T>A (p.Phe1421Leu) c.3894T>A (p.Phe1298Leu) n.4263T>A | |
| 13 | g.32338618T>C | CA019859 | BRCA2 | c.4263T>C (p.Phe1421=) c.3894T>C (p.Phe1298=) n.4263T>C | ClinVar dbSNP |
| 13 | g.32338618T>G | CA387780507 | BRCA2 | c.4263T>G (p.Phe1421Leu) c.3894T>G (p.Phe1298Leu) n.4263T>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338618T= | CA2082809981 | BRCA2 | c.4263T= (p.Phe1421=) c.3894T= (p.Phe1298=) n.4263T= | |
| 13 | g.32338618_32338620delinsTGA | CA2082809986 | BRCA2 | c.4263_4265delinsTGA (p.Phe1421=) c.3894_3896delinsTGA (p.Phe1298=) n.4263_4265delinsTGA | |
| 13 | g.32338619G>A | CA387780511 | BRCA2 | c.4264G>A (p.Glu1422Lys) c.3895G>A (p.Glu1299Lys) n.4264G>A | dbSNP |
| 13 | g.32338619G>C | CA387780514 | BRCA2 | c.4264G>C (p.Glu1422Gln) c.3895G>C (p.Glu1299Gln) n.4264G>C | dbSNP |
| 13 | g.32338619G>T | CA387780515 | BRCA2 | c.4264G>T (p.Glu1422Ter) c.3895G>T (p.Glu1299Ter) n.4264G>T | ClinVar dbSNP |
| 13 | g.32338621_32338622del | CA658656339 | BRCA2 | c.4266_4267del (p.Glu1422AspfsTer3) c.3897_3898del (p.Glu1299AspfsTer3) n.4266_4267del | ClinVar dbSNP |
| 13 | g.32338620A= | CA2082809996 | BRCA2 | c.4265A= (p.Glu1422=) c.3896A= (p.Glu1299=) n.4265A= | |
| 13 | g.32338620A>C | CA387780518 | BRCA2 | c.4265A>C (p.Glu1422Ala) c.3896A>C (p.Glu1299Ala) n.4265A>C | dbSNP |
| 13 | g.32338620A>G | CA387780520 | BRCA2 | c.4265A>G (p.Glu1422Gly) c.3896A>G (p.Glu1299Gly) n.4265A>G | dbSNP |
| 13 | g.32338620A>T | CA387780523 | BRCA2 | c.4265A>T (p.Glu1422Val) c.3896A>T (p.Glu1299Val) n.4265A>T | ClinVar dbSNP |
| 13 | g.32338621G>A | CA483438009 | BRCA2 | c.4266G>A (p.Glu1422=) c.3897G>A (p.Glu1299=) n.4266G>A | ClinVar dbSNP |
| 13 | g.32338621G>C | CA387780526 | BRCA2 | c.4266G>C (p.Glu1422Asp) c.3897G>C (p.Glu1299Asp) n.4266G>C | ClinVar dbSNP |
| 13 | g.32338621G= | CA2082810000 | BRCA2 | c.4266G= (p.Glu1422=) c.3897G= (p.Glu1299=) n.4266G= | |
| 13 | g.32338621G>T | CA387780527 | BRCA2 | c.4266G>T (p.Glu1422Asp) c.3897G>T (p.Glu1299Asp) n.4266G>T | dbSNP gnomAD v4 |
| 13 | g.32338622A= | CA2082810005 | BRCA2 | c.4267A= (p.Thr1423=) c.3898A= (p.Thr1300=) n.4267A= | |
| 13 | g.32338622A>C | CA387780528 | BRCA2 | c.4267A>C (p.Thr1423Pro) c.3898A>C (p.Thr1300Pro) n.4267A>C | dbSNP |
| 13 | g.32338622A>G | CA6940765 | BRCA2 | c.4267A>G (p.Thr1423Ala) c.3898A>G (p.Thr1300Ala) n.4267A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338622A>T | CA387780531 | BRCA2 | c.4267A>T (p.Thr1423Ser) c.3898A>T (p.Thr1300Ser) n.4267A>T | dbSNP |
| 13 | g.32338623C>A | CA387780532 | BRCA2 | c.4268C>A (p.Thr1423Asn) c.3899C>A (p.Thr1300Asn) n.4268C>A | dbSNP |
| 13 | g.32338623C= | CA2082810009 | BRCA2 | c.4268C= (p.Thr1423=) c.3899C= (p.Thr1300=) n.4268C= | |
| 13 | g.32338623C>G | CA387780535 | BRCA2 | c.4268C>G (p.Thr1423Ser) c.3899C>G (p.Thr1300Ser) n.4268C>G | dbSNP |
| 13 | g.32338623C>T | CA387780533 | BRCA2 | c.4268C>T (p.Thr1423Ile) c.3899C>T (p.Thr1300Ile) n.4268C>T | ClinVar dbSNP |
| 13 | g.32338624T>A | CA483438012 | BRCA2 | c.4269T>A (p.Thr1423=) c.3900T>A (p.Thr1300=) n.4269T>A | dbSNP |
| 13 | g.32338624T>C | CA019873 | BRCA2 | c.4269T>C (p.Thr1423=) c.3900T>C (p.Thr1300=) n.4269T>C | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338624T>G | CA483438016 | BRCA2 | c.4269T>G (p.Thr1423=) c.3900T>G (p.Thr1300=) n.4269T>G | ClinVar dbSNP |
| 13 | g.32338624T= | CA2082810018 | BRCA2 | c.4269T= (p.Thr1423=) c.3900T= (p.Thr1300=) n.4269T= | |
| 13 | g.32338625dup | CA658683807 | BRCA2 | c.4270dup (p.Ser1424PhefsTer2) c.3901dup (p.Ser1301PhefsTer2) n.4270dup | ClinVar dbSNP |
| 13 | g.32338625T>A | CA387780552 | BRCA2 | c.4270T>A (p.Ser1424Thr) c.3901T>A (p.Ser1301Thr) n.4270T>A | dbSNP |
| 13 | g.32338625T>C | CA387780554 | BRCA2 | c.4270T>C (p.Ser1424Pro) c.3901T>C (p.Ser1301Pro) n.4270T>C | dbSNP |
| 13 | g.32338625T>G | CA387780556 | BRCA2 | c.4270T>G (p.Ser1424Ala) c.3901T>G (p.Ser1301Ala) n.4270T>G | |
| 13 | g.32338625_32338626delinsTC | CA2082810028 | BRCA2 | c.4270_4271delinsTC (p.Ser1424=) c.3901_3902delinsTC (p.Ser1301=) n.4270_4271delinsTC | |
| 13 | g.32338626del | CA019882 | BRCA2 | c.4271del (p.Ser1424LeufsTer24) c.3902del (p.Ser1301LeufsTer24) n.4271del | ClinVar dbSNP |
| 13 | g.32338626C>A | CA387780558 | BRCA2 | c.4271C>A (p.Ser1424Tyr) c.3902C>A (p.Ser1301Tyr) n.4271C>A | dbSNP |
| 13 | g.32338626C= | CA2082810039 | BRCA2 | c.4271C= (p.Ser1424=) c.3902C= (p.Ser1301=) n.4271C= | |
| 13 | g.32338626C>G | CA019877 | BRCA2 | c.4271C>G (p.Ser1424Cys) c.3902C>G (p.Ser1301Cys) n.4271C>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338626C>T | CA387780560 | BRCA2 | c.4271C>T (p.Ser1424Phe) c.3902C>T (p.Ser1301Phe) n.4271C>T | dbSNP |
| 13 | g.32338626_32338628del | CA2622601024 | BRCA2 | c.4271_4273del (p.Ser1424_Asp1425delinsTyr) c.3902_3904del (p.Ser1301_Asp1302delinsTyr) n.4271_4273del | gnomAD v4 |
| 13 | g.32338627T>A | CA483438116 | BRCA2 | c.4272T>A (p.Ser1424=) c.3903T>A (p.Ser1301=) n.4272T>A | dbSNP |
| 13 | g.32338627T>C | CA483438114 | BRCA2 | c.4272T>C (p.Ser1424=) c.3903T>C (p.Ser1301=) n.4272T>C | ClinVar COSMIC COSMIC |
| 13 | g.32338627T>G | CA483438113 | BRCA2 | c.4272T>G (p.Ser1424=) c.3903T>G (p.Ser1301=) n.4272T>G | |
| 13 | g.32338627_32338628delinsTG | CA2082810044 | BRCA2 | c.4272_4273delinsTG (p.Ser1424=) c.3903_3904delinsTG (p.Ser1301=) n.4272_4273delinsTG | |
| 13 | g.32338628del | CA16613968 | BRCA2 | c.4273del (p.Asp1425IlefsTer23) c.3904del (p.Asp1302IlefsTer23) n.4273del | ClinVar dbSNP |
| 13 | g.32338628G>A | CA387780563 | BRCA2 | c.4273G>A (p.Asp1425Asn) c.3904G>A (p.Asp1302Asn) n.4273G>A | ClinVar dbSNP |
| 13 | g.32338628G>C | CA387780565 | BRCA2 | c.4273G>C (p.Asp1425His) c.3904G>C (p.Asp1302His) n.4273G>C | dbSNP COSMIC COSMIC |
| 13 | g.32338628G>T | CA387780568 | BRCA2 | c.4273G>T (p.Asp1425Tyr) c.3904G>T (p.Asp1302Tyr) n.4273G>T | |
| 13 | g.32338629A= | CA2082810062 | BRCA2 | c.4274A= (p.Asp1425=) c.3905A= (p.Asp1302=) n.4274A= | |
| 13 | g.32338629A>C | CA387780570 | BRCA2 | c.4274A>C (p.Asp1425Ala) c.3905A>C (p.Asp1302Ala) n.4274A>C | ClinVar |
| 13 | g.32338629A>G | CA019888 | BRCA2 | c.4274A>G (p.Asp1425Gly) c.3905A>G (p.Asp1302Gly) n.4274A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338629A>T | CA387780575 | BRCA2 | c.4274A>T (p.Asp1425Val) c.3905A>T (p.Asp1302Val) n.4274A>T | ClinVar dbSNP |
| 13 | g.32338630T>A | CA387780577 | BRCA2 | c.4275T>A (p.Asp1425Glu) c.3906T>A (p.Asp1302Glu) n.4275T>A | ClinVar dbSNP |
| 13 | g.32338630T>C | CA483438122 | BRCA2 | c.4275T>C (p.Asp1425=) c.3906T>C (p.Asp1302=) n.4275T>C | |
| 13 | g.32338630T>G | CA387780578 | BRCA2 | c.4275T>G (p.Asp1425Glu) c.3906T>G (p.Asp1302Glu) n.4275T>G | dbSNP |
| 13 | g.32338630T= | CA2082810069 | BRCA2 | c.4275T= (p.Asp1425=) c.3906T= (p.Asp1302=) n.4275T= | |
| 13 | g.32338631A= | CA2082810081 | BRCA2 | c.4276A= (p.Thr1426=) c.3907A= (p.Thr1303=) n.4276A= | |
| 13 | g.32338631A>C | CA387780581 | BRCA2 | c.4276A>C (p.Thr1426Pro) c.3907A>C (p.Thr1303Pro) n.4276A>C | |
| 13 | g.32338631A>G | CA10579606 | BRCA2 | c.4276A>G (p.Thr1426Ala) c.3907A>G (p.Thr1303Ala) n.4276A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338631A>T | CA387780586 | BRCA2 | c.4276A>T (p.Thr1426Ser) c.3907A>T (p.Thr1303Ser) n.4276A>T | dbSNP |
| 13 | g.32338631dup | CA019892 | BRCA2 | c.4276dup (p.Thr1426AsnfsTer12) c.3907dup (p.Thr1303AsnfsTer12) n.4276dup | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338631_32338632delinsAC | CA2082810079 | BRCA2 | c.4276_4277delinsAC (p.Thr1426=) c.3907_3908delinsAC (p.Thr1303=) n.4276_4277delinsAC |