| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32337757_32337774del | CA2580087071 | BRCA2 | c.3402_3419del (p.Tyr1135_Ser1140del) c.3033_3050del (p.Tyr1012_Ser1017del) n.3402_3419del | ClinVar |
| 13 | g.32337761_32337774delinsATATTGCAGAAGAG | CA2082816853 | BRCA2 | c.3406_3419delinsATATTGCAGAAGAG (p.Ile1136=) c.3037_3050delinsATATTGCAGAAGAG (p.Ile1013=) n.3406_3419delinsATATTGCAGAAGAG | |
| 13 | g.32337764_32337776del | CA10589202 | BRCA2 | c.3409_3421del (p.Leu1137HisfsTer9) c.3040_3052del (p.Leu1014HisfsTer9) n.3409_3421del | ClinVar dbSNP |
| 13 | g.32337769_32337775delinsGAAGAGT | CA2082816947 | BRCA2 | c.3414_3420delinsGAAGAGT (p.Gln1138=) c.3045_3051delinsGAAGAGT (p.Gln1015=) n.3414_3420delinsGAAGAGT | |
| 13 | g.32337770_32337775delinsG | CA915948451 | BRCA2 | c.3415_3420delinsG (p.Lys1139AspfsTer3) c.3046_3051delinsG (p.Lys1016AspfsTer3) n.3415_3420delinsG | ClinVar dbSNP |
| 13 | g.32337772G>A | CA017974 | BRCA2 | c.3417G>A (p.Lys1139=) c.3048G>A (p.Lys1016=) n.3417G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337772G>C | CA387776503 | BRCA2 | c.3417G>C (p.Lys1139Asn) c.3048G>C (p.Lys1016Asn) n.3417G>C | dbSNP |
| 13 | g.32337772G= | CA2082816989 | BRCA2 | c.3417G= (p.Lys1139=) c.3048G= (p.Lys1016=) n.3417G= | |
| 13 | g.32337772G>T | CA10584442 | BRCA2 | c.3417G>T (p.Lys1139Asn) c.3048G>T (p.Lys1016Asn) n.3417G>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 13 | g.32337773A= | CA2082817003 | BRCA2 | c.3418A= (p.Ser1140=) c.3049A= (p.Ser1017=) n.3418A= | |
| 13 | g.32337773A>C | CA387776506 | BRCA2 | c.3418A>C (p.Ser1140Arg) c.3049A>C (p.Ser1017Arg) n.3418A>C | gnomAD v4 |
| 13 | g.32337773A>G | CA387776508 | BRCA2 | c.3418A>G (p.Ser1140Gly) c.3049A>G (p.Ser1017Gly) n.3418A>G | ClinVar dbSNP |
| 13 | g.32337773A>T | CA387776509 | BRCA2 | c.3418A>T (p.Ser1140Cys) c.3049A>T (p.Ser1017Cys) n.3418A>T | dbSNP |
| 13 | g.32337774_32337776del | CA2825002127 | BRCA2 | c.3419_3421del (p.Ser1140del) c.3050_3052del (p.Ser1017del) n.3419_3421del | ClinVar |
| 13 | g.32337774G>A | CA387776510 | BRCA2 | c.3419G>A (p.Ser1140Asn) c.3050G>A (p.Ser1017Asn) n.3419G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337774G>C | CA017980 | BRCA2 | c.3419G>C (p.Ser1140Thr) c.3050G>C (p.Ser1017Thr) n.3419G>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32337774G= | CA2082817012 | BRCA2 | c.3419G= (p.Ser1140=) c.3050G= (p.Ser1017=) n.3419G= | |
| 13 | g.32337774G>T | CA387776516 | BRCA2 | c.3419G>T (p.Ser1140Ile) c.3050G>T (p.Ser1017Ile) n.3419G>T | dbSNP |
| 13 | g.32337775T>A | CA387776518 | BRCA2 | c.3420T>A (p.Ser1140Arg) c.3051T>A (p.Ser1017Arg) n.3420T>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337775T>C | CA017989 | BRCA2 | c.3420T>C (p.Ser1140=) c.3051T>C (p.Ser1017=) n.3420T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337775T>G | CA387776519 | BRCA2 | c.3420T>G (p.Ser1140Arg) c.3051T>G (p.Ser1017Arg) n.3420T>G | dbSNP |
| 13 | g.32337775T= | CA2082817028 | BRCA2 | c.3420T= (p.Ser1140=) c.3051T= (p.Ser1017=) n.3420T= | |
| 13 | g.32337775dup | CA2695218184 | BRCA2 | c.3420dup (p.Thr1141TyrfsTer3) c.3051dup (p.Thr1018TyrfsTer3) n.3420dup | |
| 13 | g.32337776A>C | CA387776523 | BRCA2 | c.3421A>C (p.Thr1141Pro) c.3052A>C (p.Thr1018Pro) n.3421A>C | dbSNP |
| 13 | g.32337776A>G | CA387776524 | BRCA2 | c.3421A>G (p.Thr1141Ala) c.3052A>G (p.Thr1018Ala) n.3421A>G | dbSNP |
| 13 | g.32337776A>T | CA387776521 | BRCA2 | c.3421A>T (p.Thr1141Ser) c.3052A>T (p.Thr1018Ser) n.3421A>T | dbSNP |
| 13 | g.32337776_32337777delinsAC | CA2082817038 | BRCA2 | c.3421_3422delinsAC (p.Thr1141=) c.3052_3053delinsAC (p.Thr1018=) n.3421_3422delinsAC | |
| 13 | g.32337777del | CA10585893 | BRCA2 | c.3422del (p.Thr1141AsnfsTer9) c.3053del (p.Thr1018AsnfsTer9) n.3422del | ClinVar dbSNP |
| 13 | g.32337777C>A | CA387776526 | BRCA2 | c.3422C>A (p.Thr1141Lys) c.3053C>A (p.Thr1018Lys) n.3422C>A | dbSNP |
| 13 | g.32337777C= | CA2082817050 | BRCA2 | c.3422C= (p.Thr1141=) c.3053C= (p.Thr1018=) n.3422C= | |
| 13 | g.32337777C>G | CA387776527 | BRCA2 | c.3422C>G (p.Thr1141Arg) c.3053C>G (p.Thr1018Arg) n.3422C>G | dbSNP |
| 13 | g.32337777C>T | CA017995 | BRCA2 | c.3422C>T (p.Thr1141Ile) c.3053C>T (p.Thr1018Ile) n.3422C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32337778A= | CA2082817056 | BRCA2 | c.3423A= (p.Thr1141=) c.3054A= (p.Thr1018=) n.3423A= | |
| 13 | g.32337778A>C | CA483437439 | BRCA2 | c.3423A>C (p.Thr1141=) c.3054A>C (p.Thr1018=) n.3423A>C | ClinVar dbSNP |
| 13 | g.32337778A>G | CA16606782 | BRCA2 | c.3423A>G (p.Thr1141=) c.3054A>G (p.Thr1018=) n.3423A>G | ClinVar dbSNP |
| 13 | g.32337778A>T | CA483437440 | BRCA2 | c.3423A>T (p.Thr1141=) c.3054A>T (p.Thr1018=) n.3423A>T | |
| 13 | g.32337779T>A | CA387776535 | BRCA2 | c.3424T>A (p.Phe1142Ile) c.3055T>A (p.Phe1019Ile) n.3424T>A | dbSNP |
| 13 | g.32337779T>C | CA387776533 | BRCA2 | c.3424T>C (p.Phe1142Leu) c.3055T>C (p.Phe1019Leu) n.3424T>C | ClinVar dbSNP |
| 13 | g.32337779T>G | CA387776532 | BRCA2 | c.3424T>G (p.Phe1142Val) c.3055T>G (p.Phe1019Val) n.3424T>G | |
| 13 | g.32337779T= | CA2082817060 | BRCA2 | c.3424T= (p.Phe1142=) c.3055T= (p.Phe1019=) n.3424T= | |
| 13 | g.32337780T>A | CA387776537 | BRCA2 | c.3425T>A (p.Phe1142Tyr) c.3056T>A (p.Phe1019Tyr) n.3425T>A | dbSNP |
| 13 | g.32337780T>C | CA387776538 | BRCA2 | c.3425T>C (p.Phe1142Ser) c.3056T>C (p.Phe1019Ser) n.3425T>C | dbSNP |
| 13 | g.32337780T>G | CA387776541 | BRCA2 | c.3425T>G (p.Phe1142Cys) c.3056T>G (p.Phe1019Cys) n.3425T>G | |
| 13 | g.32337781T>A | CA387776543 | BRCA2 | c.3426T>A (p.Phe1142Leu) c.3057T>A (p.Phe1019Leu) n.3426T>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337781T>C | CA6940695 | BRCA2 | c.3426T>C (p.Phe1142=) c.3057T>C (p.Phe1019=) n.3426T>C | ClinVar dbSNP ExAC gnomAD v2 |
| 13 | g.32337781T>G | CA387776545 | BRCA2 | c.3426T>G (p.Phe1142Leu) c.3057T>G (p.Phe1019Leu) n.3426T>G | |
| 13 | g.32337781T= | CA2082817073 | BRCA2 | c.3426T= (p.Phe1142=) c.3057T= (p.Phe1019=) n.3426T= | |
| 13 | g.32337782G>A | CA387776546 | BRCA2 | c.3427G>A (p.Glu1143Lys) c.3058G>A (p.Glu1020Lys) n.3427G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32337782G>C | CA387776549 | BRCA2 | c.3427G>C (p.Glu1143Gln) c.3058G>C (p.Glu1020Gln) n.3427G>C | dbSNP |
| 13 | g.32337782G= | CA2082817098 | BRCA2 | c.3427G= (p.Glu1143=) c.3058G= (p.Glu1020=) n.3427G= | |
| 13 | g.32337782G>T | CA387776548 | BRCA2 | c.3427G>T (p.Glu1143Ter) c.3058G>T (p.Glu1020Ter) n.3427G>T | dbSNP |
| 13 | g.32337783A>C | CA387776550 | BRCA2 | c.3428A>C (p.Glu1143Ala) c.3059A>C (p.Glu1020Ala) n.3428A>C | |
| 13 | g.32337783A>G | CA387776553 | BRCA2 | c.3428A>G (p.Glu1143Gly) c.3059A>G (p.Glu1020Gly) n.3428A>G | dbSNP |
| 13 | g.32337783A>T | CA387776555 | BRCA2 | c.3428A>T (p.Glu1143Val) c.3059A>T (p.Glu1020Val) n.3428A>T | dbSNP |
| 13 | g.32337784A>C | CA387776561 | BRCA2 | c.3429A>C (p.Glu1143Asp) c.3060A>C (p.Glu1020Asp) n.3429A>C | |
| 13 | g.32337784A>G | CA483437449 | BRCA2 | c.3429A>G (p.Glu1143=) c.3060A>G (p.Glu1020=) n.3429A>G | dbSNP |
| 13 | g.32337784A>T | CA387776562 | BRCA2 | c.3429A>T (p.Glu1143Asp) c.3060A>T (p.Glu1020Asp) n.3429A>T | dbSNP COSMIC |
| 13 | g.32337784_32337785delinsAG | CA2082817105 | BRCA2 | c.3429_3430delinsAG (p.Glu1143=) c.3060_3061delinsAG (p.Glu1020=) n.3429_3430delinsAG | |
| 13 | g.32337785del | CA915948452 | BRCA2 | c.3430del (p.Val1144CysfsTer6) c.3061del (p.Val1021CysfsTer6) n.3430del | ClinVar dbSNP |
| 13 | g.32337785G>A | CA387776564 | BRCA2 | c.3430G>A (p.Val1144Met) c.3061G>A (p.Val1021Met) n.3430G>A | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32337785G>C | CA387776565 | BRCA2 | c.3430G>C (p.Val1144Leu) c.3061G>C (p.Val1021Leu) n.3430G>C | dbSNP |
| 13 | g.32337785G= | CA2082817116 | BRCA2 | c.3430G= (p.Val1144=) c.3061G= (p.Val1021=) n.3430G= | |
| 13 | g.32337785G>T | CA387776567 | BRCA2 | c.3430G>T (p.Val1144Leu) c.3061G>T (p.Val1021Leu) n.3430G>T | |
| 13 | g.32337786T>A | CA387776569 | BRCA2 | c.3431T>A (p.Val1144Glu) c.3062T>A (p.Val1021Glu) n.3431T>A | dbSNP |
| 13 | g.32337786T>C | CA387776571 | BRCA2 | c.3431T>C (p.Val1144Ala) c.3062T>C (p.Val1021Ala) n.3431T>C | ClinVar |
| 13 | g.32337786T>G | CA017998 | BRCA2 | c.3431T>G (p.Val1144Gly) c.3062T>G (p.Val1021Gly) n.3431T>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32337786T= | CA2082817122 | BRCA2 | c.3431T= (p.Val1144=) c.3062T= (p.Val1021=) n.3431T= | |
| 13 | g.32337786_32337788delinsTGC | CA2082817131 | BRCA2 | c.3431_3433delinsTGC (p.Val1144=) c.3062_3064delinsTGC (p.Val1021=) n.3431_3433delinsTGC | |
| 13 | g.32337787G>A | CA483437454 | BRCA2 | c.3432G>A (p.Val1144=) c.3063G>A (p.Val1021=) n.3432G>A | ClinVar dbSNP |
| 13 | g.32337787G>C | CA6940696 | BRCA2 | c.3432G>C (p.Val1144=) c.3063G>C (p.Val1021=) n.3432G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32337787G= | CA2082817144 | BRCA2 | c.3432G= (p.Val1144=) c.3063G= (p.Val1021=) n.3432G= | |
| 13 | g.32337787G>T | CA483437456 | BRCA2 | c.3432G>T (p.Val1144=) c.3063G>T (p.Val1021=) n.3432G>T | |
| 13 | g.32337787_32337788del | CA919242448 | BRCA2 | c.3432_3433del (p.Pro1145Ter) c.3063_3064del (p.Pro1022Ter) n.3432_3433del | dbSNP |
| 13 | g.32337788C>A | CA387776575 | BRCA2 | c.3433C>A (p.Pro1145Thr) c.3064C>A (p.Pro1022Thr) n.3433C>A | dbSNP |
| 13 | g.32337788C= | CA2082817154 | BRCA2 | c.3433C= (p.Pro1145=) c.3064C= (p.Pro1022=) n.3433C= | |
| 13 | g.32337788C>G | CA387776577 | BRCA2 | c.3433C>G (p.Pro1145Ala) c.3064C>G (p.Pro1022Ala) n.3433C>G | ClinVar dbSNP |
| 13 | g.32337788C>T | CA387776580 | BRCA2 | c.3433C>T (p.Pro1145Ser) c.3064C>T (p.Pro1022Ser) n.3433C>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337789C>A | CA387776583 | BRCA2 | c.3434C>A (p.Pro1145His) c.3065C>A (p.Pro1022His) n.3434C>A | dbSNP |
| 13 | g.32337789C= | CA2082817162 | BRCA2 | c.3434C= (p.Pro1145=) c.3065C= (p.Pro1022=) n.3434C= | |
| 13 | g.32337789C>G | CA387776591 | BRCA2 | c.3434C>G (p.Pro1145Arg) c.3065C>G (p.Pro1022Arg) n.3434C>G | ClinVar dbSNP |
| 13 | g.32337789C>T | CA018004 | BRCA2 | c.3434C>T (p.Pro1145Leu) c.3065C>T (p.Pro1022Leu) n.3434C>T | ClinVar dbSNP |
| 13 | g.32337790T>A | CA483437458 | BRCA2 | c.3435T>A (p.Pro1145=) c.3066T>A (p.Pro1022=) n.3435T>A | |
| 13 | g.32337790T>C | CA483437461 | BRCA2 | c.3435T>C (p.Pro1145=) c.3066T>C (p.Pro1022=) n.3435T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337790T>G | CA483437460 | BRCA2 | c.3435T>G (p.Pro1145=) c.3066T>G (p.Pro1022=) n.3435T>G | |
| 13 | g.32337790T= | CA2082817171 | BRCA2 | c.3435T= (p.Pro1145=) c.3066T= (p.Pro1022=) n.3435T= | |
| 13 | g.32337791G>A | CA387776594 | BRCA2 | c.3436G>A (p.Glu1146Lys) c.3067G>A (p.Glu1023Lys) n.3436G>A | ClinVar dbSNP |
| 13 | g.32337791G>C | CA387776597 | BRCA2 | c.3436G>C (p.Glu1146Gln) c.3067G>C (p.Glu1023Gln) n.3436G>C | |
| 13 | g.32337791G= | CA2082817176 | BRCA2 | c.3436G= (p.Glu1146=) c.3067G= (p.Glu1023=) n.3436G= | |
| 13 | g.32337791G>T | CA387776599 | BRCA2 | c.3436G>T (p.Glu1146Ter) c.3067G>T (p.Glu1023Ter) n.3436G>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32337792A= | CA2082817191 | BRCA2 | c.3437A= (p.Glu1146=) c.3068A= (p.Glu1023=) n.3437A= | |
| 13 | g.32337792A>C | CA387776602 | BRCA2 | c.3437A>C (p.Glu1146Ala) c.3068A>C (p.Glu1023Ala) n.3437A>C | |
| 13 | g.32337792A>G | CA018008 | BRCA2 | c.3437A>G (p.Glu1146Gly) c.3068A>G (p.Glu1023Gly) n.3437A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32337792A>T | CA10576065 | BRCA2 | c.3437A>T (p.Glu1146Val) c.3068A>T (p.Glu1023Val) n.3437A>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337795del | CA2580087075 | BRCA2 | c.3440del (p.Asn1147ThrfsTer3) c.3071del (p.Asn1024ThrfsTer3) n.3440del | ClinVar |
| 13 | g.32337793A>C | CA387776608 | BRCA2 | c.3438A>C (p.Glu1146Asp) c.3069A>C (p.Glu1023Asp) n.3438A>C | |
| 13 | g.32337793A>G | CA483437463 | BRCA2 | c.3438A>G (p.Glu1146=) c.3069A>G (p.Glu1023=) n.3438A>G | |
| 13 | g.32337793A>T | CA387776610 | BRCA2 | c.3438A>T (p.Glu1146Asp) c.3069A>T (p.Glu1023Asp) n.3438A>T | dbSNP |
| 13 | g.32337794A>C | CA387776611 | BRCA2 | c.3439A>C (p.Asn1147His) c.3070A>C (p.Asn1024His) n.3439A>C | |
| 13 | g.32337794A>G | CA387776612 | BRCA2 | c.3439A>G (p.Asn1147Asp) c.3070A>G (p.Asn1024Asp) n.3439A>G | dbSNP |
| 13 | g.32337794A>T | CA387776615 | BRCA2 | c.3439A>T (p.Asn1147Tyr) c.3070A>T (p.Asn1024Tyr) n.3439A>T | dbSNP |
| 13 | g.32337795A= | CA2018046951 | BRCA2 | c.3440A= (p.Asn1147=) c.3071A= (p.Asn1024=) n.3440A= | |
| 13 | g.32337795A>C | CA387776618 | BRCA2 | c.3440A>C (p.Asn1147Thr) c.3071A>C (p.Asn1024Thr) n.3440A>C | |
| 13 | g.32337795A>G | CA247505007 | BRCA2 | c.3440A>G (p.Asn1147Ser) c.3071A>G (p.Asn1024Ser) n.3440A>G | dbSNP |
| 13 | g.32337795A>T | CA387776620 | BRCA2 | c.3440A>T (p.Asn1147Ile) c.3071A>T (p.Asn1024Ile) n.3440A>T | ClinVar |
| 13 | g.32337796C>A | CA387776622 | BRCA2 | c.3441C>A (p.Asn1147Lys) c.3072C>A (p.Asn1024Lys) n.3441C>A | dbSNP COSMIC COSMIC |
| 13 | g.32337796C>G | CA387776625 | BRCA2 | c.3441C>G (p.Asn1147Lys) c.3072C>G (p.Asn1024Lys) n.3441C>G | dbSNP |
| 13 | g.32337796C>T | CA483437466 | BRCA2 | c.3441C>T (p.Asn1147=) c.3072C>T (p.Asn1024=) n.3441C>T | dbSNP |
| 13 | g.32337797C>A | CA387776628 | BRCA2 | c.3442C>A (p.Gln1148Lys) c.3073C>A (p.Gln1025Lys) n.3442C>A | dbSNP |
| 13 | g.32337797C= | CA2082817207 | BRCA2 | c.3442C= (p.Gln1148=) c.3073C= (p.Gln1025=) n.3442C= | |
| 13 | g.32337797C>G | CA387776630 | BRCA2 | c.3442C>G (p.Gln1148Glu) c.3073C>G (p.Gln1025Glu) n.3442C>G | dbSNP |
| 13 | g.32337797C>T | CA018022 | BRCA2 | c.3442C>T (p.Gln1148Ter) c.3073C>T (p.Gln1025Ter) n.3442C>T | ClinVar dbSNP |
| 13 | g.32337798A= | CA2082817218 | BRCA2 | c.3443A= (p.Gln1148=) c.3074A= (p.Gln1025=) n.3443A= | |
| 13 | g.32337798A>C | CA387776642 | BRCA2 | c.3443A>C (p.Gln1148Pro) c.3074A>C (p.Gln1025Pro) n.3443A>C | |
| 13 | g.32337798A>G | CA018029 | BRCA2 | c.3443A>G (p.Gln1148Arg) c.3074A>G (p.Gln1025Arg) n.3443A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337798A>T | CA387776645 | BRCA2 | c.3443A>T (p.Gln1148Leu) c.3074A>T (p.Gln1025Leu) n.3443A>T | ClinVar dbSNP |
| 13 | g.32337799G>A | CA483437472 | BRCA2 | c.3444G>A (p.Gln1148=) c.3075G>A (p.Gln1025=) n.3444G>A | dbSNP |
| 13 | g.32337799G>C | CA387776646 | BRCA2 | c.3444G>C (p.Gln1148His) c.3075G>C (p.Gln1025His) n.3444G>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337799G= | CA2082817228 | BRCA2 | c.3444G= (p.Gln1148=) c.3075G= (p.Gln1025=) n.3444G= | |
| 13 | g.32337799G>T | CA387776648 | BRCA2 | c.3444G>T (p.Gln1148His) c.3075G>T (p.Gln1025His) n.3444G>T | dbSNP |
| 13 | g.32337800A= | CA2082817242 | BRCA2 | c.3445A= (p.Met1149=) c.3076A= (p.Met1026=) n.3445A= | |
| 13 | g.32337800A>C | CA387776650 | BRCA2 | c.3445A>C (p.Met1149Leu) c.3076A>C (p.Met1026Leu) n.3445A>C | |
| 13 | g.32337800A>G | CA018035 | BRCA2 | c.3445A>G (p.Met1149Val) c.3076A>G (p.Met1026Val) n.3445A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337800A>T | CA387776653 | BRCA2 | c.3445A>T (p.Met1149Leu) c.3076A>T (p.Met1026Leu) n.3445A>T | ClinVar dbSNP |
| 13 | g.32337800_32337801dup | CA2499222132 | BRCA2 | c.3445_3446dup (p.Met1149IlefsTer2) c.3076_3077dup (p.Met1026IlefsTer2) n.3445_3446dup | |
| 13 | g.32337801T>A | CA387776656 | BRCA2 | c.3446T>A (p.Met1149Lys) c.3077T>A (p.Met1026Lys) n.3446T>A | dbSNP gnomAD v4 |
| 13 | g.32337801T>C | CA018041 | BRCA2 | c.3446T>C (p.Met1149Thr) c.3077T>C (p.Met1026Thr) n.3446T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337801T>G | CA387776660 | BRCA2 | c.3446T>G (p.Met1149Arg) c.3077T>G (p.Met1026Arg) n.3446T>G | dbSNP |
| 13 | g.32337801T= | CA2082817247 | BRCA2 | c.3446T= (p.Met1149=) c.3077T= (p.Met1026=) n.3446T= | |
| 13 | g.32337801dup | CA2697551772 | BRCA2 | c.3446dup (p.Met1149IlefsTer9) c.3077dup (p.Met1026IlefsTer9) n.3446dup | ClinVar |
| 13 | g.32337802del | CA2580087076 | BRCA2 | c.3447del (p.Met1149IlefsTer4) c.3078del (p.Met1026IlefsTer4) n.3447del | ClinVar |
| 13 | g.32337802G>A | CA10579578 | BRCA2 | c.3447G>A (p.Met1149Ile) c.3078G>A (p.Met1026Ile) n.3447G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32337802G>C | CA387776663 | BRCA2 | c.3447G>C (p.Met1149Ile) c.3078G>C (p.Met1026Ile) n.3447G>C | dbSNP |
| 13 | g.32337802G= | CA2082817268 | BRCA2 | c.3447G= (p.Met1149=) c.3078G= (p.Met1026=) n.3447G= | |
| 13 | g.32337802G>T | CA387776665 | BRCA2 | c.3447G>T (p.Met1149Ile) c.3078G>T (p.Met1026Ile) n.3447G>T | dbSNP gnomAD v4 |
| 13 | g.32337803A= | CA2082817278 | BRCA2 | c.3448A= (p.Thr1150=) c.3079A= (p.Thr1027=) n.3448A= | |
| 13 | g.32337803A>C | CA387776668 | BRCA2 | c.3448A>C (p.Thr1150Pro) c.3079A>C (p.Thr1027Pro) n.3448A>C | |
| 13 | g.32337803A>G | CA387776669 | BRCA2 | c.3448A>G (p.Thr1150Ala) c.3079A>G (p.Thr1027Ala) n.3448A>G | ClinVar dbSNP |
| 13 | g.32337803A>T | CA247505019 | BRCA2 | c.3448A>T (p.Thr1150Ser) c.3079A>T (p.Thr1027Ser) n.3448A>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337803_32337804insAG | CA658823667 | BRCA2 | c.3448_3449insAG (p.Thr1150LysfsTer4) c.3079_3080insAG (p.Thr1027LysfsTer4) n.3448_3449insAG | ClinVar dbSNP |
| 13 | g.32337804del | CA2697551773 | BRCA2 | c.3449del (p.Thr1150IlefsTer3) c.3080del (p.Thr1027IlefsTer3) n.3449del | ClinVar |
| 13 | g.32337804C>A | CA387776671 | BRCA2 | c.3449C>A (p.Thr1150Asn) c.3080C>A (p.Thr1027Asn) n.3449C>A | dbSNP |
| 13 | g.32337804C= | CA2082817289 | BRCA2 | c.3449C= (p.Thr1150=) c.3080C= (p.Thr1027=) n.3449C= | |
| 13 | g.32337804C>G | CA018054 | BRCA2 | c.3449C>G (p.Thr1150Ser) c.3080C>G (p.Thr1027Ser) n.3449C>G | ClinVar dbSNP |
| 13 | g.32337804C>T | CA387776675 | BRCA2 | c.3449C>T (p.Thr1150Ile) c.3080C>T (p.Thr1027Ile) n.3449C>T | ClinVar dbSNP |
| 13 | g.32337804_32337806delinsCTA | CA2082817286 | BRCA2 | c.3449_3451delinsCTA (p.Thr1150=) c.3080_3082delinsCTA (p.Thr1027=) n.3449_3451delinsCTA | |
| 13 | g.32337806_32337809del | CA2499222133 | BRCA2 | c.3451_3454del (p.Ile1151Ter) c.3082_3085del (p.Ile1028Ter) n.3451_3454del | ClinVar dbSNP |
| 13 | g.32337804_32337805insAG | CA018047 | BRCA2 | c.3449_3450insAG (p.Ile1151ValfsTer3) c.3080_3081insAG (p.Ile1028ValfsTer3) n.3449_3450insAG | ClinVar dbSNP |
| 13 | g.32337805T>A | CA483437482 | BRCA2 | c.3450T>A (p.Thr1150=) c.3081T>A (p.Thr1027=) n.3450T>A | dbSNP gnomAD v4 |
| 13 | g.32337805T>C | CA483437483 | BRCA2 | c.3450T>C (p.Thr1150=) c.3081T>C (p.Thr1027=) n.3450T>C | ClinVar dbSNP |
| 13 | g.32337805T>G | CA483437484 | BRCA2 | c.3450T>G (p.Thr1150=) c.3081T>G (p.Thr1027=) n.3450T>G | |
| 13 | g.32337805T= | CA2082817328 | BRCA2 | c.3450T= (p.Thr1150=) c.3081T= (p.Thr1027=) n.3450T= | |
| 13 | g.32337805dup | CA16619697 | BRCA2 | c.3450dup (p.Ile1151TyrfsTer7) c.3081dup (p.Ile1028TyrfsTer7) n.3450dup | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32337806_32337807del | CA10589203 | BRCA2 | c.3451_3452del (p.Ile1151LeufsTer6) c.3082_3083del (p.Ile1028LeufsTer6) n.3451_3452del | ClinVar dbSNP |
| 13 | g.32337806A= | CA2082817348 | BRCA2 | c.3451A= (p.Ile1151=) c.3082A= (p.Ile1028=) n.3451A= | |
| 13 | g.32337806A>C | CA018059 | BRCA2 | c.3451A>C (p.Ile1151Leu) c.3082A>C (p.Ile1028Leu) n.3451A>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32337806A>G | CA018064 | BRCA2 | c.3451A>G (p.Ile1151Val) c.3082A>G (p.Ile1028Val) n.3451A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337806A>T | CA6940697 | BRCA2 | c.3451A>T (p.Ile1151Phe) c.3082A>T (p.Ile1028Phe) n.3451A>T | dbSNP ExAC gnomAD v2 |
| 13 | g.32337806_32337810delinsATCTT | CA2082817353 | BRCA2 | c.3451_3455delinsATCTT (p.Ile1151=) c.3082_3086delinsATCTT (p.Ile1028=) n.3451_3455delinsATCTT | |
| 13 | g.32337807T>A | CA387776687 | BRCA2 | c.3452T>A (p.Ile1151Asn) c.3083T>A (p.Ile1028Asn) n.3452T>A | dbSNP |
| 13 | g.32337807T>C | CA387776684 | BRCA2 | c.3452T>C (p.Ile1151Thr) c.3083T>C (p.Ile1028Thr) n.3452T>C | dbSNP |
| 13 | g.32337807T>G | CA387776688 | BRCA2 | c.3452T>G (p.Ile1151Ser) c.3083T>G (p.Ile1028Ser) n.3452T>G | dbSNP |
| 13 | g.32337807dup | CA018072 | BRCA2 | c.3452dup (p.Thr1154AspfsTer4) c.3083dup (p.Thr1031AspfsTer4) n.3452dup | ClinVar dbSNP |
| 13 | g.32337807_32337808delinsTC | CA2082817364 | BRCA2 | c.3452_3453delinsTC (p.Ile1151=) c.3083_3084delinsTC (p.Ile1028=) n.3452_3453delinsTC | |
| 13 | g.32337807_32337810del | CA658683864 | BRCA2 | c.3452_3455del (p.Ile1151LysfsTer16) c.3083_3086del (p.Ile1028LysfsTer16) n.3452_3455del | ClinVar dbSNP |
| 13 | g.32337808del | CA018090 | BRCA2 | c.3453del (p.Leu1152Ter) c.3084del (p.Leu1029Ter) n.3453del | ClinVar dbSNP |
| 13 | g.32337808C>A | CA483437487 | BRCA2 | c.3453C>A (p.Ile1151=) c.3084C>A (p.Ile1028=) n.3453C>A | |
| 13 | g.32337808C= | CA2082817374 | BRCA2 | c.3453C= (p.Ile1151=) c.3084C= (p.Ile1028=) n.3453C= | |
| 13 | g.32337808C>G | CA018084 | BRCA2 | c.3453C>G (p.Ile1151Met) c.3084C>G (p.Ile1028Met) n.3453C>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32337808C>T | CA483437490 | BRCA2 | c.3453C>T (p.Ile1151=) c.3084C>T (p.Ile1028=) n.3453C>T | |
| 13 | g.32337808_32337810delinsCTT | CA2082817381 | BRCA2 | c.3453_3455delinsCTT (p.Ile1151=) c.3084_3086delinsCTT (p.Ile1028=) n.3453_3455delinsCTT | |
| 13 | g.32337809T>A | CA387776692 | BRCA2 | c.3454T>A (p.Leu1152Ile) c.3085T>A (p.Leu1029Ile) n.3454T>A | dbSNP |
| 13 | g.32337809T>C | CA483437491 | BRCA2 | c.3454T>C (p.Leu1152=) c.3085T>C (p.Leu1029=) n.3454T>C | |
| 13 | g.32337809T>G | CA387776697 | BRCA2 | c.3454T>G (p.Leu1152Val) c.3085T>G (p.Leu1029Val) n.3454T>G | |
| 13 | g.32337809_32337810del | CA645372956 | BRCA2 | c.3454_3455del (p.Leu1152LysfsTer5) c.3085_3086del (p.Leu1029LysfsTer5) n.3454_3455del | ClinVar dbSNP |
| 13 | g.32337810dup | CA018080 | BRCA2 | c.3455dup (p.Leu1152PhefsTer6) c.3086dup (p.Leu1029PhefsTer6) n.3455dup | ClinVar dbSNP |
| 13 | g.32337809_32337810dup | CA658656410 | BRCA2 | c.3454_3455dup (p.Leu1152PhefsTer2) c.3085_3086dup (p.Leu1029PhefsTer2) n.3454_3455dup | ClinVar dbSNP |
| 13 | g.32337810T>A | CA10579579 | BRCA2 | c.3455T>A (p.Leu1152Ter) c.3086T>A (p.Leu1029Ter) n.3455T>A | ClinVar dbSNP |
| 13 | g.32337810T>C | CA387776701 | BRCA2 | c.3455T>C (p.Leu1152Ser) c.3086T>C (p.Leu1029Ser) n.3455T>C | ClinVar dbSNP |
| 13 | g.32337810T>G | CA018097 | BRCA2 | c.3455T>G (p.Leu1152Ter) c.3086T>G (p.Leu1029Ter) n.3455T>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32337810T= | CA2082817412 | BRCA2 | c.3455T= (p.Leu1152=) c.3086T= (p.Leu1029=) n.3455T= | |
| 13 | g.32337810_32337811delinsTA | CA2082817408 | BRCA2 | c.3455_3456delinsTA (p.Leu1152=) c.3086_3087delinsTA (p.Leu1029=) n.3455_3456delinsTA | |
| 13 | g.32337811A= | CA2082817429 | BRCA2 | c.3456A= (p.Leu1152=) c.3087A= (p.Leu1029=) n.3456A= | |
| 13 | g.32337811A>C | CA387776702 | BRCA2 | c.3456A>C (p.Leu1152Phe) c.3087A>C (p.Leu1029Phe) n.3456A>C | |
| 13 | g.32337811A>G | CA483437496 | BRCA2 | c.3456A>G (p.Leu1152=) c.3087A>G (p.Leu1029=) n.3456A>G | ClinVar dbSNP |
| 13 | g.32337811A>T | CA387776703 | BRCA2 | c.3456A>T (p.Leu1152Phe) c.3087A>T (p.Leu1029Phe) n.3456A>T | dbSNP |
| 13 | g.32337813dup | CA916080526 | BRCA2 | c.3458dup (p.Thr1154AspfsTer4) c.3089dup (p.Thr1031AspfsTer4) n.3458dup | ClinVar dbSNP |
| 13 | g.32337813del | CA018110 | BRCA2 | c.3458del (p.Lys1153ArgfsTer15) c.3089del (p.Lys1030ArgfsTer15) n.3458del | ClinVar dbSNP |
| 13 | g.32337812A= | CA2082817441 | BRCA2 | c.3457A= (p.Lys1153=) c.3088A= (p.Lys1030=) n.3457A= | |
| 13 | g.32337812A>C | CA387776704 | BRCA2 | c.3457A>C (p.Lys1153Gln) c.3088A>C (p.Lys1030Gln) n.3457A>C | |
| 13 | g.32337812A>G | CA387776707 | BRCA2 | c.3457A>G (p.Lys1153Glu) c.3088A>G (p.Lys1030Glu) n.3457A>G | |
| 13 | g.32337812A>T | CA387776723 | BRCA2 | c.3457A>T (p.Lys1153Ter) c.3088A>T (p.Lys1030Ter) n.3457A>T | dbSNP |
| 13 | g.32337812_32337813insG | CA919242453 | BRCA2 | c.3457_3458insG (p.Lys1153ArgfsTer5) c.3088_3089insG (p.Lys1030ArgfsTer5) n.3457_3458insG | dbSNP |
| 13 | g.32337813A= | CA2082817452 | BRCA2 | c.3458A= (p.Lys1153=) c.3089A= (p.Lys1030=) n.3458A= | |
| 13 | g.32337813A>C | CA387776726 | BRCA2 | c.3458A>C (p.Lys1153Thr) c.3089A>C (p.Lys1030Thr) n.3458A>C | |
| 13 | g.32337813A>G | CA018105 | BRCA2 | c.3458A>G (p.Lys1153Arg) c.3089A>G (p.Lys1030Arg) n.3458A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337813A>T | CA387776731 | BRCA2 | c.3458A>T (p.Lys1153Met) c.3089A>T (p.Lys1030Met) n.3458A>T | dbSNP |
| 13 | g.32337814G>A | CA483437498 | BRCA2 | c.3459G>A (p.Lys1153=) c.3090G>A (p.Lys1030=) n.3459G>A | ClinVar dbSNP |
| 13 | g.32337814G>C | CA387776734 | BRCA2 | c.3459G>C (p.Lys1153Asn) c.3090G>C (p.Lys1030Asn) n.3459G>C | dbSNP |
| 13 | g.32337814G>T | CA387776737 | BRCA2 | c.3459G>T (p.Lys1153Asn) c.3090G>T (p.Lys1030Asn) n.3459G>T | dbSNP gnomAD v4 |
| 13 | g.32337815del | CA2580614698 | BRCA2 | c.3460del (p.Thr1154ProfsTer14) c.3091del (p.Thr1031ProfsTer14) n.3460del | ClinVar |
| 13 | g.32337815A= | CA2082817459 | BRCA2 | c.3460A= (p.Thr1154=) c.3091A= (p.Thr1031=) n.3460A= | |
| 13 | g.32337815A>C | CA387776738 | BRCA2 | c.3460A>C (p.Thr1154Pro) c.3091A>C (p.Thr1031Pro) n.3460A>C | |
| 13 | g.32337815A>G | CA387776739 | BRCA2 | c.3460A>G (p.Thr1154Ala) c.3091A>G (p.Thr1031Ala) n.3460A>G | ClinVar dbSNP |
| 13 | g.32337815A>T | CA387776742 | BRCA2 | c.3460A>T (p.Thr1154Ser) c.3091A>T (p.Thr1031Ser) n.3460A>T | ClinVar dbSNP |
| 13 | g.32337815_32337816delinsAC | CA2082817458 | BRCA2 | c.3460_3461delinsAC (p.Thr1154=) c.3091_3092delinsAC (p.Thr1031=) n.3460_3461delinsAC | |
| 13 | g.32337815_32337816insG | CA2695199689 | BRCA2 | c.3460_3461insG (p.Thr1154SerfsTer4) c.3091_3092insG (p.Thr1031SerfsTer4) n.3460_3461insG | ClinVar |
| 13 | g.32337816C>A | CA387776743 | BRCA2 | c.3461C>A (p.Thr1154Asn) c.3092C>A (p.Thr1031Asn) n.3461C>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337816C= | CA2082817473 | BRCA2 | c.3461C= (p.Thr1154=) c.3092C= (p.Thr1031=) n.3461C= | |
| 13 | g.32337816C>G | CA387776744 | BRCA2 | c.3461C>G (p.Thr1154Ser) c.3092C>G (p.Thr1031Ser) n.3461C>G | dbSNP gnomAD v4 |
| 13 | g.32337816C>T | CA018115 | BRCA2 | c.3461C>T (p.Thr1154Ile) c.3092C>T (p.Thr1031Ile) n.3461C>T | ClinVar dbSNP |
| 13 | g.32337817del | CA658656411 | BRCA2 | c.3462del (p.Thr1155LeufsTer13) c.3093del (p.Thr1032LeufsTer13) n.3462del | ClinVar dbSNP |
| 13 | g.32337817C>A | CA483437502 | BRCA2 | c.3462C>A (p.Thr1154=) c.3093C>A (p.Thr1031=) n.3462C>A | dbSNP |
| 13 | g.32337817C= | CA2082817478 | BRCA2 | c.3462C= (p.Thr1154=) c.3093C= (p.Thr1031=) n.3462C= | |
| 13 | g.32337817C>G | CA018119 | BRCA2 | c.3462C>G (p.Thr1154=) c.3093C>G (p.Thr1031=) n.3462C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337817C>T | CA018124 | BRCA2 | c.3462C>T (p.Thr1154=) c.3093C>T (p.Thr1031=) n.3462C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337818A= | CA2082817485 | BRCA2 | c.3463A= (p.Thr1155=) c.3094A= (p.Thr1032=) n.3463A= | |
| 13 | g.32337818A>C | CA387776750 | BRCA2 | c.3463A>C (p.Thr1155Pro) c.3094A>C (p.Thr1032Pro) n.3463A>C | ClinVar dbSNP |
| 13 | g.32337818A>G | CA387776752 | BRCA2 | c.3463A>G (p.Thr1155Ala) c.3094A>G (p.Thr1032Ala) n.3463A>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32337818A>T | CA387776753 | BRCA2 | c.3463A>T (p.Thr1155Ser) c.3094A>T (p.Thr1032Ser) n.3463A>T | dbSNP |
| 13 | g.32337819C>A | CA387776760 | BRCA2 | c.3464C>A (p.Thr1155Asn) c.3095C>A (p.Thr1032Asn) n.3464C>A | dbSNP |
| 13 | g.32337819C= | CA2082817496 | BRCA2 | c.3464C= (p.Thr1155=) c.3095C= (p.Thr1032=) n.3464C= | |
| 13 | g.32337819C>G | CA387776761 | BRCA2 | c.3464C>G (p.Thr1155Ser) c.3095C>G (p.Thr1032Ser) n.3464C>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32337819C>T | CA387776758 | BRCA2 | c.3464C>T (p.Thr1155Ile) c.3095C>T (p.Thr1032Ile) n.3464C>T | dbSNP |
| 13 | g.32337819_32337821delinsCTT | CA2082817498 | BRCA2 | c.3464_3466delinsCTT (p.Thr1155=) c.3095_3097delinsCTT (p.Thr1032=) n.3464_3466delinsCTT | |
| 13 | g.32337820T>A | CA483437507 | BRCA2 | c.3465T>A (p.Thr1155=) c.3096T>A (p.Thr1032=) n.3465T>A | dbSNP |
| 13 | g.32337820T>C | CA483437505 | BRCA2 | c.3465T>C (p.Thr1155=) c.3096T>C (p.Thr1032=) n.3465T>C | ClinVar dbSNP |
| 13 | g.32337820T>G | CA483437509 | BRCA2 | c.3465T>G (p.Thr1155=) c.3096T>G (p.Thr1032=) n.3465T>G | ClinVar |
| 13 | g.32337820T= | CA2082817517 | BRCA2 | c.3465T= (p.Thr1155=) c.3096T= (p.Thr1032=) n.3465T= | |
| 13 | g.32337820_32337821del | CA018127 | BRCA2 | c.3465_3466del (p.Ser1156Ter) c.3096_3097del (p.Ser1033Ter) n.3465_3466del | ClinVar dbSNP |
| 13 | g.32337821del | CA2581463421 | BRCA2 | c.3466del (p.Ser1156LeufsTer12) c.3097del (p.Ser1033LeufsTer12) n.3466del | |
| 13 | g.32337821T>A | CA387776773 | BRCA2 | c.3466T>A (p.Ser1156Thr) c.3097T>A (p.Ser1033Thr) n.3466T>A | dbSNP |
| 13 | g.32337821T>C | CA387776775 | BRCA2 | c.3466T>C (p.Ser1156Pro) c.3097T>C (p.Ser1033Pro) n.3466T>C | |
| 13 | g.32337821T>G | CA387776780 | BRCA2 | c.3466T>G (p.Ser1156Ala) c.3097T>G (p.Ser1033Ala) n.3466T>G | ClinVar dbSNP |
| 13 | g.32337821_32337822delinsTC | CA2082817520 | BRCA2 | c.3466_3467delinsTC (p.Ser1156=) c.3097_3098delinsTC (p.Ser1033=) n.3466_3467delinsTC | |
| 13 | g.32337822del | CA919242455 | BRCA2 | c.3467del (p.Ser1156LeufsTer12) c.3098del (p.Ser1033LeufsTer12) n.3467del | ClinVar dbSNP |
| 13 | g.32337822C>A | CA387776782 | BRCA2 | c.3467C>A (p.Ser1156Tyr) c.3098C>A (p.Ser1033Tyr) n.3467C>A | |
| 13 | g.32337822C= | CA2082817525 | BRCA2 | c.3467C= (p.Ser1156=) c.3098C= (p.Ser1033=) n.3467C= | |
| 13 | g.32337822C>G | CA387776784 | BRCA2 | c.3467C>G (p.Ser1156Cys) c.3098C>G (p.Ser1033Cys) n.3467C>G | dbSNP |
| 13 | g.32337822C>T | CA6940698 | BRCA2 | c.3467C>T (p.Ser1156Phe) c.3098C>T (p.Ser1033Phe) n.3467C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32337823T>A | CA483437514 | BRCA2 | c.3468T>A (p.Ser1156=) c.3099T>A (p.Ser1033=) n.3468T>A | |
| 13 | g.32337823T>C | CA483437516 | BRCA2 | c.3468T>C (p.Ser1156=) c.3099T>C (p.Ser1033=) n.3468T>C | ClinVar |
| 13 | g.32337823T>G | CA483437517 | BRCA2 | c.3468T>G (p.Ser1156=) c.3099T>G (p.Ser1033=) n.3468T>G | |
| 13 | g.32337823dup | CA2573053807 | BRCA2 | c.3468dup (p.Glu1157Ter) c.3099dup (p.Glu1034Ter) n.3468dup | ClinVar dbSNP |
| 13 | g.32337824G>A | CA387776787 | BRCA2 | c.3469G>A (p.Glu1157Lys) c.3100G>A (p.Glu1034Lys) n.3469G>A | |
| 13 | g.32337824G>C | CA387776788 | BRCA2 | c.3469G>C (p.Glu1157Gln) c.3100G>C (p.Glu1034Gln) n.3469G>C | |
| 13 | g.32337824G= | CA2082817545 | BRCA2 | c.3469G= (p.Glu1157=) c.3100G= (p.Glu1034=) n.3469G= | |
| 13 | g.32337824G>T | CA018132 | BRCA2 | c.3469G>T (p.Glu1157Ter) c.3100G>T (p.Glu1034Ter) n.3469G>T | ClinVar dbSNP |
| 13 | g.32337825A= | CA2082817557 | BRCA2 | c.3470A= (p.Glu1157=) c.3101A= (p.Glu1034=) n.3470A= | |
| 13 | g.32337825A>C | CA387776791 | BRCA2 | c.3470A>C (p.Glu1157Ala) c.3101A>C (p.Glu1034Ala) n.3470A>C | |
| 13 | g.32337825A>G | CA387776795 | BRCA2 | c.3470A>G (p.Glu1157Gly) c.3101A>G (p.Glu1034Gly) n.3470A>G | dbSNP |
| 13 | g.32337825A>T | CA387776796 | BRCA2 | c.3470A>T (p.Glu1157Val) c.3101A>T (p.Glu1034Val) n.3470A>T | ClinVar dbSNP |
| 13 | g.32337826G>A | CA483437523 | BRCA2 | c.3471G>A (p.Glu1157=) c.3102G>A (p.Glu1034=) n.3471G>A | dbSNP |
| 13 | g.32337826G>C | CA6940699 | BRCA2 | c.3471G>C (p.Glu1157Asp) c.3102G>C (p.Glu1034Asp) n.3471G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32337826G= | CA2082817563 | BRCA2 | c.3471G= (p.Glu1157=) c.3102G= (p.Glu1034=) n.3471G= | |
| 13 | g.32337826G>T | CA387776798 | BRCA2 | c.3471G>T (p.Glu1157Asp) c.3102G>T (p.Glu1034Asp) n.3471G>T | dbSNP |
| 13 | g.32337827G>A | CA387776802 | BRCA2 | c.3472G>A (p.Glu1158Lys) c.3103G>A (p.Glu1035Lys) n.3472G>A | ClinVar dbSNP |
| 13 | g.32337827G>C | CA387776805 | BRCA2 | c.3472G>C (p.Glu1158Gln) c.3103G>C (p.Glu1035Gln) n.3472G>C | dbSNP COSMIC COSMIC |
| 13 | g.32337827G= | CA2082817576 | BRCA2 | c.3472G= (p.Glu1158=) c.3103G= (p.Glu1035=) n.3472G= | |
| 13 | g.32337827G>T | CA387776807 | BRCA2 | c.3472G>T (p.Glu1158Ter) c.3103G>T (p.Glu1035Ter) n.3472G>T | ClinVar dbSNP |
| 13 | g.32337828A= | CA2082817589 | BRCA2 | c.3473A= (p.Glu1158=) c.3104A= (p.Glu1035=) n.3473A= | |
| 13 | g.32337828A>C | CA387776810 | BRCA2 | c.3473A>C (p.Glu1158Ala) c.3104A>C (p.Glu1035Ala) n.3473A>C | |
| 13 | g.32337828A>G | CA10575915 | BRCA2 | c.3473A>G (p.Glu1158Gly) c.3104A>G (p.Glu1035Gly) n.3473A>G | ClinVar dbSNP |
| 13 | g.32337828A>T | CA387776816 | BRCA2 | c.3473A>T (p.Glu1158Val) c.3104A>T (p.Glu1035Val) n.3473A>T | dbSNP |
| 13 | g.32337829A= | CA2082817604 | BRCA2 | c.3474A= (p.Glu1158=) c.3105A= (p.Glu1035=) n.3474A= | |
| 13 | g.32337829A>C | CA387776818 | BRCA2 | c.3474A>C (p.Glu1158Asp) c.3105A>C (p.Glu1035Asp) n.3474A>C | |
| 13 | g.32337829A>G | CA483437529 | BRCA2 | c.3474A>G (p.Glu1158=) c.3105A>G (p.Glu1035=) n.3474A>G | ClinVar dbSNP |
| 13 | g.32337829A>T | CA387776819 | BRCA2 | c.3474A>T (p.Glu1158Asp) c.3105A>T (p.Glu1035Asp) n.3474A>T | dbSNP |
| 13 | g.32337830T>A | CA387776821 | BRCA2 | c.3475T>A (p.Cys1159Ser) c.3106T>A (p.Cys1036Ser) n.3475T>A | dbSNP COSMIC COSMIC |
| 13 | g.32337830T>C | CA387776824 | BRCA2 | c.3475T>C (p.Cys1159Arg) c.3106T>C (p.Cys1036Arg) n.3475T>C | ClinVar dbSNP |
| 13 | g.32337830T>G | CA10575916 | BRCA2 | c.3475T>G (p.Cys1159Gly) c.3106T>G (p.Cys1036Gly) n.3475T>G | ClinVar dbSNP |
| 13 | g.32337830T= | CA2082817620 | BRCA2 | c.3475T= (p.Cys1159=) c.3106T= (p.Cys1036=) n.3475T= | |
| 13 | g.32337831del | CA2580087083 | BRCA2 | c.3476del (p.Cys1159SerfsTer9) c.3107del (p.Cys1036SerfsTer9) n.3476del | ClinVar |
| 13 | g.32337831G>A | CA387776828 | BRCA2 | c.3476G>A (p.Cys1159Tyr) c.3107G>A (p.Cys1036Tyr) n.3476G>A | ClinVar dbSNP COSMIC COSMIC |
| 13 | g.32337831G>C | CA387776829 | BRCA2 | c.3476G>C (p.Cys1159Ser) c.3107G>C (p.Cys1036Ser) n.3476G>C | |
| 13 | g.32337831G>T | CA387776831 | BRCA2 | c.3476G>T (p.Cys1159Phe) c.3107G>T (p.Cys1036Phe) n.3476G>T | ClinVar |
| 13 | g.32337832C>A | CA018138 | BRCA2 | c.3477C>A (p.Cys1159Ter) c.3108C>A (p.Cys1036Ter) n.3477C>A | ClinVar dbSNP |
| 13 | g.32337832C= | CA2082817638 | BRCA2 | c.3477C= (p.Cys1159=) c.3108C= (p.Cys1036=) n.3477C= | |
| 13 | g.32337832C>G | CA387776834 | BRCA2 | c.3477C>G (p.Cys1159Trp) c.3108C>G (p.Cys1036Trp) n.3477C>G | dbSNP |
| 13 | g.32337832C>T | CA483437535 | BRCA2 | c.3477C>T (p.Cys1159=) c.3108C>T (p.Cys1036=) n.3477C>T | ClinVar dbSNP |
| 13 | g.32337832_32337836delinsCAGAG | CA2082817640 | BRCA2 | c.3477_3481delinsCAGAG (p.Cys1159=) c.3108_3112delinsCAGAG (p.Cys1036=) n.3477_3481delinsCAGAG | |
| 13 | g.32337833A= | CA2082817659 | BRCA2 | c.3478A= (p.Arg1160=) c.3109A= (p.Arg1037=) n.3478A= | |
| 13 | g.32337833A>C | CA483437536 | BRCA2 | c.3478A>C (p.Arg1160=) c.3109A>C (p.Arg1037=) n.3478A>C | gnomAD v4 |
| 13 | g.32337833A>G | CA387776837 | BRCA2 | c.3478A>G (p.Arg1160Gly) c.3109A>G (p.Arg1037Gly) n.3478A>G | ClinVar dbSNP |
| 13 | g.32337833A>T | CA387776840 | BRCA2 | c.3478A>T (p.Arg1160Ter) c.3109A>T (p.Arg1037Ter) n.3478A>T | dbSNP |
| 13 | g.32337833_32337836delinsTGAGGA | CA16614286 | BRCA2 | c.3478_3481delinsTGAGGA (p.Arg1160Ter) c.3109_3112delinsTGAGGA (p.Arg1037Ter) n.3478_3481delinsTGAGGA | ClinVar dbSNP |
| 13 | g.32337836_32337837dup | CA10583089 | BRCA2 | c.3481_3482dup (p.Asp1161GlufsTer8) c.3112_3113dup (p.Asp1038GlufsTer8) n.3481_3482dup | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32337836_32337837del | CA2580614699 | BRCA2 | c.3481_3482del (p.Asp1161CysfsTer2) c.3112_3113del (p.Asp1038CysfsTer2) n.3481_3482del | ClinVar |
| 13 | g.32337834_32337837del | CA2580618297 | BRCA2 | c.3479_3482del (p.Arg1160MetfsTer7) c.3110_3113del (p.Arg1037MetfsTer7) n.3479_3482del | |
| 13 | g.32337834G>A | CA018145 | BRCA2 | c.3479G>A (p.Arg1160Lys) c.3110G>A (p.Arg1037Lys) n.3479G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337834G>C | CA387776843 | BRCA2 | c.3479G>C (p.Arg1160Thr) c.3110G>C (p.Arg1037Thr) n.3479G>C | dbSNP |
| 13 | g.32337834G= | CA2082817669 | BRCA2 | c.3479G= (p.Arg1160=) c.3110G= (p.Arg1037=) n.3479G= | |
| 13 | g.32337834G>T | CA387776846 | BRCA2 | c.3479G>T (p.Arg1160Ile) c.3110G>T (p.Arg1037Ile) n.3479G>T | dbSNP |
| 13 | g.32337835A= | CA2082817679 | BRCA2 | c.3480A= (p.Arg1160=) c.3111A= (p.Arg1037=) n.3480A= | |
| 13 | g.32337835A>C | CA387776850 | BRCA2 | c.3480A>C (p.Arg1160Ser) c.3111A>C (p.Arg1037Ser) n.3480A>C | |
| 13 | g.32337835A>G | CA483437541 | BRCA2 | c.3480A>G (p.Arg1160=) c.3111A>G (p.Arg1037=) n.3480A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337835A>T | CA387776851 | BRCA2 | c.3480A>T (p.Arg1160Ser) c.3111A>T (p.Arg1037Ser) n.3480A>T | dbSNP |
| 13 | g.32337835_32337846delinsAGATGCTGATCT | CA2082817684 | BRCA2 | c.3480_3491delinsAGATGCTGATCT (p.Arg1160=) c.3111_3122delinsAGATGCTGATCT (p.Arg1037=) n.3480_3491delinsAGATGCTGATCT | |
| 13 | g.32337836G>A | CA387776859 | BRCA2 | c.3481G>A (p.Asp1161Asn) c.3112G>A (p.Asp1038Asn) n.3481G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337836G>C | CA387776861 | BRCA2 | c.3481G>C (p.Asp1161His) c.3112G>C (p.Asp1038His) n.3481G>C | dbSNP gnomAD v4 |
| 13 | g.32337836G= | CA2082817698 | BRCA2 | c.3481G= (p.Asp1161=) c.3112G= (p.Asp1038=) n.3481G= | |
| 13 | g.32337836G>T | CA387776865 | BRCA2 | c.3481G>T (p.Asp1161Tyr) c.3112G>T (p.Asp1038Tyr) n.3481G>T | |
| 13 | g.32337836_32337846del | CA645372957 | BRCA2 | c.3481_3491del (p.Asp1161SerfsTer19) c.3112_3122del (p.Asp1038SerfsTer19) n.3481_3491del | ClinVar dbSNP |
| 13 | g.32337837A= | CA2082817703 | BRCA2 | c.3482A= (p.Asp1161=) c.3113A= (p.Asp1038=) n.3482A= | |
| 13 | g.32337837A>C | CA387776867 | BRCA2 | c.3482A>C (p.Asp1161Ala) c.3113A>C (p.Asp1038Ala) n.3482A>C | |
| 13 | g.32337837A>G | CA16614289 | BRCA2 | c.3482A>G (p.Asp1161Gly) c.3113A>G (p.Asp1038Gly) n.3482A>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32337837A>T | CA387776870 | BRCA2 | c.3482A>T (p.Asp1161Val) c.3113A>T (p.Asp1038Val) n.3482A>T | ClinVar dbSNP |
| 13 | g.32337838T>A | CA387776872 | BRCA2 | c.3483T>A (p.Asp1161Glu) c.3114T>A (p.Asp1038Glu) n.3483T>A | dbSNP |
| 13 | g.32337838T>C | CA483437545 | BRCA2 | c.3483T>C (p.Asp1161=) c.3114T>C (p.Asp1038=) n.3483T>C | ClinVar dbSNP |
| 13 | g.32337838T>G | CA387776875 | BRCA2 | c.3483T>G (p.Asp1161Glu) c.3114T>G (p.Asp1038Glu) n.3483T>G | dbSNP gnomAD v4 |
| 13 | g.32337839G>A | CA10583090 | BRCA2 | c.3484G>A (p.Ala1162Thr) c.3115G>A (p.Ala1039Thr) n.3484G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337839G>C | CA387776880 | BRCA2 | c.3484G>C (p.Ala1162Pro) c.3115G>C (p.Ala1039Pro) n.3484G>C | dbSNP |
| 13 | g.32337839G= | CA2082817708 | BRCA2 | c.3484G= (p.Ala1162=) c.3115G= (p.Ala1039=) n.3484G= | |
| 13 | g.32337839G>T | CA387776879 | BRCA2 | c.3484G>T (p.Ala1162Ser) c.3115G>T (p.Ala1039Ser) n.3484G>T | |
| 13 | g.32337840C>A | CA387776883 | BRCA2 | c.3485C>A (p.Ala1162Asp) c.3116C>A (p.Ala1039Asp) n.3485C>A | dbSNP |
| 13 | g.32337840C= | CA2082817717 | BRCA2 | c.3485C= (p.Ala1162=) c.3116C= (p.Ala1039=) n.3485C= | |
| 13 | g.32337840C>G | CA387776885 | BRCA2 | c.3485C>G (p.Ala1162Gly) c.3116C>G (p.Ala1039Gly) n.3485C>G | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32337840C>T | CA018151 | BRCA2 | c.3485C>T (p.Ala1162Val) c.3116C>T (p.Ala1039Val) n.3485C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32337841T>A | CA483437547 | BRCA2 | c.3486T>A (p.Ala1162=) c.3117T>A (p.Ala1039=) n.3486T>A | dbSNP |
| 13 | g.32337841T>C | CA483437549 | BRCA2 | c.3486T>C (p.Ala1162=) c.3117T>C (p.Ala1039=) n.3486T>C | ClinVar dbSNP |
| 13 | g.32337841T>G | CA483437548 | BRCA2 | c.3486T>G (p.Ala1162=) c.3117T>G (p.Ala1039=) n.3486T>G | |
| 13 | g.32337841_32337842delinsTG | CA2082817730 | BRCA2 | c.3486_3487delinsTG (p.Ala1162=) c.3117_3118delinsTG (p.Ala1039=) n.3486_3487delinsTG | |
| 13 | g.32337842del | CA018156 | BRCA2 | c.3487del (p.Asp1163IlefsTer5) c.3118del (p.Asp1040IlefsTer5) n.3487del | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337842G>A | CA387776888 | BRCA2 | c.3487G>A (p.Asp1163Asn) c.3118G>A (p.Asp1040Asn) n.3487G>A | ClinVar dbSNP |
| 13 | g.32337842G>C | CA387776890 | BRCA2 | c.3487G>C (p.Asp1163His) c.3118G>C (p.Asp1040His) n.3487G>C | dbSNP |
| 13 | g.32337842G>T | CA387776893 | BRCA2 | c.3487G>T (p.Asp1163Tyr) c.3118G>T (p.Asp1040Tyr) n.3487G>T | dbSNP |
| 13 | g.32337843A>C | CA387776897 | BRCA2 | c.3488A>C (p.Asp1163Ala) c.3119A>C (p.Asp1040Ala) n.3488A>C | dbSNP |
| 13 | g.32337843A>G | CA387776899 | BRCA2 | c.3488A>G (p.Asp1163Gly) c.3119A>G (p.Asp1040Gly) n.3488A>G | dbSNP |
| 13 | g.32337843A>T | CA387776902 | BRCA2 | c.3488A>T (p.Asp1163Val) c.3119A>T (p.Asp1040Val) n.3488A>T | dbSNP |
| 13 | g.32337843_32337844delinsAT | CA2082817752 | BRCA2 | c.3488_3489delinsAT (p.Asp1163=) c.3119_3120delinsAT (p.Asp1040=) n.3488_3489delinsAT | |
| 13 | g.32337843_32337846delinsATCT | CA2082817743 | BRCA2 | c.3488_3491delinsATCT (p.Asp1163=) c.3119_3122delinsATCT (p.Asp1040=) n.3488_3491delinsATCT | |
| 13 | g.32337844del | CA10589204 | BRCA2 | c.3489del (p.Leu1164PhefsTer4) c.3120del (p.Leu1041PhefsTer4) n.3489del | ClinVar dbSNP |
| 13 | g.32337844T>A | CA387776904 | BRCA2 | c.3489T>A (p.Asp1163Glu) c.3120T>A (p.Asp1040Glu) n.3489T>A | ClinVar dbSNP |
| 13 | g.32337844T>C | CA483437551 | BRCA2 | c.3489T>C (p.Asp1163=) c.3120T>C (p.Asp1040=) n.3489T>C | ClinVar |
| 13 | g.32337844T>G | CA387776903 | BRCA2 | c.3489T>G (p.Asp1163Glu) c.3120T>G (p.Asp1040Glu) n.3489T>G | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32337844T= | CA2082817766 | BRCA2 | c.3489T= (p.Asp1163=) c.3120T= (p.Asp1040=) n.3489T= | |
| 13 | g.32337846_32337848del | CA658683865 | BRCA2 | c.3491_3493del (p.Leu1164del) c.3122_3124del (p.Leu1041del) n.3491_3493del | ClinVar dbSNP |
| 13 | g.32337845C>A | CA387776907 | BRCA2 | c.3490C>A (p.Leu1164Ile) c.3121C>A (p.Leu1041Ile) n.3490C>A | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32337845C= | CA2082817782 | BRCA2 | c.3490C= (p.Leu1164=) c.3121C= (p.Leu1041=) n.3490C= | |
| 13 | g.32337845C>G | CA387776905 | BRCA2 | c.3490C>G (p.Leu1164Val) c.3121C>G (p.Leu1041Val) n.3490C>G | dbSNP |
| 13 | g.32337845C>T | CA387776906 | BRCA2 | c.3490C>T (p.Leu1164Phe) c.3121C>T (p.Leu1041Phe) n.3490C>T | dbSNP |
| 13 | g.32337846T>A | CA6940700 | BRCA2 | c.3491T>A (p.Leu1164His) c.3122T>A (p.Leu1041His) n.3491T>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32337846T>C | CA387776909 | BRCA2 | c.3491T>C (p.Leu1164Pro) c.3122T>C (p.Leu1041Pro) n.3491T>C | ClinVar dbSNP |
| 13 | g.32337846T>G | CA387776910 | BRCA2 | c.3491T>G (p.Leu1164Arg) c.3122T>G (p.Leu1041Arg) n.3491T>G | |
| 13 | g.32337846T= | CA2082817800 | BRCA2 | c.3491T= (p.Leu1164=) c.3122T= (p.Leu1041=) n.3491T= | |
| 13 | g.32337847dup | CA10589205 | BRCA2 | c.3492dup (p.His1165SerfsTer19) c.3123dup (p.His1042SerfsTer19) n.3492dup | ClinVar dbSNP |
| 13 | g.32337847T>A | CA483437554 | BRCA2 | c.3492T>A (p.Leu1164=) c.3123T>A (p.Leu1041=) n.3492T>A | dbSNP |
| 13 | g.32337847T>C | CA483437555 | BRCA2 | c.3492T>C (p.Leu1164=) c.3123T>C (p.Leu1041=) n.3492T>C | dbSNP |
| 13 | g.32337847T>G | CA483437556 | BRCA2 | c.3492T>G (p.Leu1164=) c.3123T>G (p.Leu1041=) n.3492T>G | |
| 13 | g.32337848del | CA2580087085 | BRCA2 | c.3493del (p.His1165MetfsTer3) c.3124del (p.His1042MetfsTer3) n.3493del | ClinVar |
| 13 | g.32337848C>A | CA387776914 | BRCA2 | c.3493C>A (p.His1165Asn) c.3124C>A (p.His1042Asn) n.3493C>A | dbSNP gnomAD v4 |
| 13 | g.32337848C>G | CA387776913 | BRCA2 | c.3493C>G (p.His1165Asp) c.3124C>G (p.His1042Asp) n.3493C>G | dbSNP |
| 13 | g.32337848C>T | CA387776912 | BRCA2 | c.3493C>T (p.His1165Tyr) c.3124C>T (p.His1042Tyr) n.3493C>T | ClinVar dbSNP COSMIC COSMIC |
| 13 | g.32337849A= | CA2082817809 | BRCA2 | c.3494A= (p.His1165=) c.3125A= (p.His1042=) n.3494A= | |
| 13 | g.32337849A>C | CA387776915 | BRCA2 | c.3494A>C (p.His1165Pro) c.3125A>C (p.His1042Pro) n.3494A>C | gnomAD v4 |
| 13 | g.32337849A>G | CA018167 | BRCA2 | c.3494A>G (p.His1165Arg) c.3125A>G (p.His1042Arg) n.3494A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337849A>T | CA387776918 | BRCA2 | c.3494A>T (p.His1165Leu) c.3125A>T (p.His1042Leu) n.3494A>T | ClinVar dbSNP |
| 13 | g.32337850T>A | CA387776921 | BRCA2 | c.3495T>A (p.His1165Gln) c.3126T>A (p.His1042Gln) n.3495T>A | dbSNP |
| 13 | g.32337850T>C | CA018171 | BRCA2 | c.3495T>C (p.His1165=) c.3126T>C (p.His1042=) n.3495T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337850T>G | CA387776924 | BRCA2 | c.3495T>G (p.His1165Gln) c.3126T>G (p.His1042Gln) n.3495T>G | ClinVar dbSNP |
| 13 | g.32337850T= | CA2082817816 | BRCA2 | c.3495T= (p.His1165=) c.3126T= (p.His1042=) n.3495T= | |
| 13 | g.32337851G>A | CA018177 | BRCA2 | c.3496G>A (p.Val1166Ile) c.3127G>A (p.Val1043Ile) n.3496G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337851G>C | CA387776926 | BRCA2 | c.3496G>C (p.Val1166Leu) c.3127G>C (p.Val1043Leu) n.3496G>C | dbSNP |
| 13 | g.32337851G= | CA2082817830 | BRCA2 | c.3496G= (p.Val1166=) c.3127G= (p.Val1043=) n.3496G= | |
| 13 | g.32337851G>T | CA387776925 | BRCA2 | c.3496G>T (p.Val1166Phe) c.3127G>T (p.Val1043Phe) n.3496G>T | dbSNP |
| 13 | g.32337851_32337852delinsGT | CA2082817832 | BRCA2 | c.3496_3497delinsGT (p.Val1166=) c.3127_3128delinsGT (p.Val1043=) n.3496_3497delinsGT | |
| 13 | g.32337851_32337854del | CA2573149319 | BRCA2 | c.3496_3499del (p.Val1166Ter) c.3127_3130del (p.Val1043Ter) n.3496_3499del | ClinVar dbSNP |
| 13 | g.32337852del | CA10589206 | BRCA2 | c.3497del (p.Val1166AlafsTer2) c.3128del (p.Val1043AlafsTer2) n.3497del | ClinVar dbSNP |
| 13 | g.32337852T>A | CA018181 | BRCA2 | c.3497T>A (p.Val1166Asp) c.3128T>A (p.Val1043Asp) n.3497T>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32337852T>C | CA6940701 | BRCA2 | c.3497T>C (p.Val1166Ala) c.3128T>C (p.Val1043Ala) n.3497T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32337852T>G | CA387776929 | BRCA2 | c.3497T>G (p.Val1166Gly) c.3128T>G (p.Val1043Gly) n.3497T>G | dbSNP |
| 13 | g.32337852T= | CA2082817856 | BRCA2 | c.3497T= (p.Val1166=) c.3128T= (p.Val1043=) n.3497T= | |
| 13 | g.32337853C>A | CA483437562 | BRCA2 | c.3498C>A (p.Val1166=) c.3129C>A (p.Val1043=) n.3498C>A | gnomAD v4 |
| 13 | g.32337853C= | CA2082817861 | BRCA2 | c.3498C= (p.Val1166=) c.3129C= (p.Val1043=) n.3498C= | |
| 13 | g.32337853C>G | CA483437563 | BRCA2 | c.3498C>G (p.Val1166=) c.3129C>G (p.Val1043=) n.3498C>G | dbSNP |
| 13 | g.32337853C>T | CA483437564 | BRCA2 | c.3498C>T (p.Val1166=) c.3129C>T (p.Val1043=) n.3498C>T | dbSNP gnomAD v4 |
| 13 | g.32337853_32337855delinsCAT | CA2082817860 | BRCA2 | c.3498_3500delinsCAT (p.Val1166=) c.3129_3131delinsCAT (p.Val1043=) n.3498_3500delinsCAT | |
| 13 | g.32337854del | CA2695202246 | BRCA2 | c.3499del (p.Ile1167Ter) c.3130del (p.Ile1044Ter) n.3499del | |
| 13 | g.32337854A= | CA2082817872 | BRCA2 | c.3499A= (p.Ile1167=) c.3130A= (p.Ile1044=) n.3499A= | |
| 13 | g.32337854A>C | CA387776932 | BRCA2 | c.3499A>C (p.Ile1167Leu) c.3130A>C (p.Ile1044Leu) n.3499A>C | dbSNP |
| 13 | g.32337854A>G | CA018187 | BRCA2 | c.3499A>G (p.Ile1167Val) c.3130A>G (p.Ile1044Val) n.3499A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32337854A>T | CA387776935 | BRCA2 | c.3499A>T (p.Ile1167Leu) c.3130A>T (p.Ile1044Leu) n.3499A>T | dbSNP |
| 13 | g.32337855_32337856del | CA018202 | BRCA2 | c.3500_3501del (p.Ile1167AsnfsTer16) c.3131_3132del (p.Ile1044AsnfsTer16) n.3500_3501del | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32337855T>A | CA387776938 | BRCA2 | c.3500T>A (p.Ile1167Lys) c.3131T>A (p.Ile1044Lys) n.3500T>A | |
| 13 | g.32337855T>C | CA387776940 | BRCA2 | c.3500T>C (p.Ile1167Thr) c.3131T>C (p.Ile1044Thr) n.3500T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337855T>G | CA387776943 | BRCA2 | c.3500T>G (p.Ile1167Arg) c.3131T>G (p.Ile1044Arg) n.3500T>G | |
| 13 | g.32337855T= | CA2082817887 | BRCA2 | c.3500T= (p.Ile1167=) c.3131T= (p.Ile1044=) n.3500T= | |
| 13 | g.32337856A= | CA2082817901 | BRCA2 | c.3501A= (p.Ile1167=) c.3132A= (p.Ile1044=) n.3501A= | |
| 13 | g.32337856A>C | CA483437571 | BRCA2 | c.3501A>C (p.Ile1167=) c.3132A>C (p.Ile1044=) n.3501A>C | |
| 13 | g.32337856A>G | CA387776945 | BRCA2 | c.3501A>G (p.Ile1167Met) c.3132A>G (p.Ile1044Met) n.3501A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337856A>T | CA483437569 | BRCA2 | c.3501A>T (p.Ile1167=) c.3132A>T (p.Ile1044=) n.3501A>T | dbSNP |
| 13 | g.32337857dup | CA10589207 | BRCA2 | c.3502dup (p.Met1168AsnfsTer16) c.3133dup (p.Met1045AsnfsTer16) n.3502dup | ClinVar dbSNP |
| 13 | g.32337857A>C | CA387776949 | BRCA2 | c.3502A>C (p.Met1168Leu) c.3133A>C (p.Met1045Leu) n.3502A>C | |
| 13 | g.32337857A>G | CA387776952 | BRCA2 | c.3502A>G (p.Met1168Val) c.3133A>G (p.Met1045Val) n.3502A>G | ClinVar dbSNP |
| 13 | g.32337857A>T | CA387776946 | BRCA2 | c.3502A>T (p.Met1168Leu) c.3133A>T (p.Met1045Leu) n.3502A>T | dbSNP |
| 13 | g.32337858T>A | CA018209 | BRCA2 | c.3503T>A (p.Met1168Lys) c.3134T>A (p.Met1045Lys) n.3503T>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32337858T>C | CA387776957 | BRCA2 | c.3503T>C (p.Met1168Thr) c.3134T>C (p.Met1045Thr) n.3503T>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32337858T>G | CA387776956 | BRCA2 | c.3503T>G (p.Met1168Arg) c.3134T>G (p.Met1045Arg) n.3503T>G | |
| 13 | g.32337858T= | CA2082817912 | BRCA2 | c.3503T= (p.Met1168=) c.3134T= (p.Met1045=) n.3503T= | |
| 13 | g.32337859G>A | CA387776960 | BRCA2 | c.3504G>A (p.Met1168Ile) c.3135G>A (p.Met1045Ile) n.3504G>A | |
| 13 | g.32337859G>C | CA387776962 | BRCA2 | c.3504G>C (p.Met1168Ile) c.3135G>C (p.Met1045Ile) n.3504G>C | |
| 13 | g.32337859G= | CA2082817926 | BRCA2 | c.3504G= (p.Met1168=) c.3135G= (p.Met1045=) n.3504G= | |
| 13 | g.32337859G>T | CA387776965 | BRCA2 | c.3504G>T (p.Met1168Ile) c.3135G>T (p.Met1045Ile) n.3504G>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337860A>C | CA387776968 | BRCA2 | c.3505A>C (p.Asn1169His) c.3136A>C (p.Asn1046His) n.3505A>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337860A>G | CA387776969 | BRCA2 | c.3505A>G (p.Asn1169Asp) c.3136A>G (p.Asn1046Asp) n.3505A>G | dbSNP |
| 13 | g.32337860A>T | CA387776973 | BRCA2 | c.3505A>T (p.Asn1169Tyr) c.3136A>T (p.Asn1046Tyr) n.3505A>T | dbSNP |
| 13 | g.32337861del | CA658761205 | BRCA2 | c.3506del (p.Asn1169MetfsTer8) c.3137del (p.Asn1046MetfsTer8) n.3506del | |
| 13 | g.32337861A= | CA2082817955 | BRCA2 | c.3506A= (p.Asn1169=) c.3137A= (p.Asn1046=) n.3506A= | |
| 13 | g.32337861A>C | CA387776976 | BRCA2 | c.3506A>C (p.Asn1169Thr) c.3137A>C (p.Asn1046Thr) n.3506A>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32337861A>G | CA387776978 | BRCA2 | c.3506A>G (p.Asn1169Ser) c.3137A>G (p.Asn1046Ser) n.3506A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337861A>T | CA387776981 | BRCA2 | c.3506A>T (p.Asn1169Ile) c.3137A>T (p.Asn1046Ile) n.3506A>T | dbSNP |
| 13 | g.32337862T>A | CA387776984 | BRCA2 | c.3507T>A (p.Asn1169Lys) c.3138T>A (p.Asn1046Lys) n.3507T>A | dbSNP |
| 13 | g.32337862T>C | CA483437587 | BRCA2 | c.3507T>C (p.Asn1169=) c.3138T>C (p.Asn1046=) n.3507T>C | gnomAD v4 |
| 13 | g.32337862T>G | CA387776986 | BRCA2 | c.3507T>G (p.Asn1169Lys) c.3138T>G (p.Asn1046Lys) n.3507T>G | |
| 13 | g.32337863G>A | CA387776992 | BRCA2 | c.3508G>A (p.Ala1170Thr) c.3139G>A (p.Ala1047Thr) n.3508G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337863G>C | CA387776989 | BRCA2 | c.3508G>C (p.Ala1170Pro) c.3139G>C (p.Ala1047Pro) n.3508G>C | |
| 13 | g.32337863G= | CA2082817962 | BRCA2 | c.3508G= (p.Ala1170=) c.3139G= (p.Ala1047=) n.3508G= | |
| 13 | g.32337863G>T | CA387776987 | BRCA2 | c.3508G>T (p.Ala1170Ser) c.3139G>T (p.Ala1047Ser) n.3508G>T | |
| 13 | g.32337863_32337864delinsGC | CA2082817967 | BRCA2 | c.3508_3509delinsGC (p.Ala1170=) c.3139_3140delinsGC (p.Ala1047=) n.3508_3509delinsGC | |
| 13 | g.32337864C>A | CA387776996 | BRCA2 | c.3509C>A (p.Ala1170Asp) c.3140C>A (p.Ala1047Asp) n.3509C>A | dbSNP |
| 13 | g.32337864C= | CA2082817973 | BRCA2 | c.3509C= (p.Ala1170=) c.3140C= (p.Ala1047=) n.3509C= | |
| 13 | g.32337864C>G | CA387776997 | BRCA2 | c.3509C>G (p.Ala1170Gly) c.3140C>G (p.Ala1047Gly) n.3509C>G | dbSNP |
| 13 | g.32337864C>T | CA018216 | BRCA2 | c.3509C>T (p.Ala1170Val) c.3140C>T (p.Ala1047Val) n.3509C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337867dup | CA2695218185 | BRCA2 | c.3512dup (p.Ser1172IlefsTer12) c.3143dup (p.Ser1049IlefsTer12) n.3512dup | ClinVar |
| 13 | g.32337867del | CA919242463 | BRCA2 | c.3512del (p.Pro1171HisfsTer6) c.3143del (p.Pro1048HisfsTer6) n.3512del | dbSNP |
| 13 | g.32337865C>A | CA483437588 | BRCA2 | c.3510C>A (p.Ala1170=) c.3141C>A (p.Ala1047=) n.3510C>A | dbSNP |
| 13 | g.32337865C= | CA2082817977 | BRCA2 | c.3510C= (p.Ala1170=) c.3141C= (p.Ala1047=) n.3510C= | |
| 13 | g.32337865C>G | CA483437589 | BRCA2 | c.3510C>G (p.Ala1170=) c.3141C>G (p.Ala1047=) n.3510C>G | dbSNP |
| 13 | g.32337865C>T | CA483437590 | BRCA2 | c.3510C>T (p.Ala1170=) c.3141C>T (p.Ala1047=) n.3510C>T | dbSNP |
| 13 | g.32337866C>A | CA387777001 | BRCA2 | c.3511C>A (p.Pro1171Thr) c.3142C>A (p.Pro1048Thr) n.3511C>A | ClinVar dbSNP |
| 13 | g.32337866C>G | CA387777003 | BRCA2 | c.3511C>G (p.Pro1171Ala) c.3142C>G (p.Pro1048Ala) n.3511C>G | dbSNP gnomAD v4 |
| 13 | g.32337866C>T | CA387777005 | BRCA2 | c.3511C>T (p.Pro1171Ser) c.3142C>T (p.Pro1048Ser) n.3511C>T | ClinVar dbSNP |
| 13 | g.32337867C>A | CA387777008 | BRCA2 | c.3512C>A (p.Pro1171Gln) c.3143C>A (p.Pro1048Gln) n.3512C>A | |
| 13 | g.32337867C= | CA2082817983 | BRCA2 | c.3512C= (p.Pro1171=) c.3143C= (p.Pro1048=) n.3512C= | |
| 13 | g.32337867C>G | CA387777009 | BRCA2 | c.3512C>G (p.Pro1171Arg) c.3143C>G (p.Pro1048Arg) n.3512C>G | |
| 13 | g.32337867C>T | CA387777012 | BRCA2 | c.3512C>T (p.Pro1171Leu) c.3143C>T (p.Pro1048Leu) n.3512C>T | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
| 13 | g.32337868A= | CA2082817989 | BRCA2 | c.3513A= (p.Pro1171=) c.3144A= (p.Pro1048=) n.3513A= | |
| 13 | g.32337868A>C | CA483437591 | BRCA2 | c.3513A>C (p.Pro1171=) c.3144A>C (p.Pro1048=) n.3513A>C | dbSNP |
| 13 | g.32337868A>G | CA16606673 | BRCA2 | c.3513A>G (p.Pro1171=) c.3144A>G (p.Pro1048=) n.3513A>G | ClinVar dbSNP |
| 13 | g.32337868A>T | CA483437592 | BRCA2 | c.3513A>T (p.Pro1171=) c.3144A>T (p.Pro1048=) n.3513A>T | dbSNP |
| 13 | g.32337869del | CA2825002128 | BRCA2 | c.3514del (p.Ser1172ArgfsTer5) c.3145del (p.Ser1049ArgfsTer5) n.3514del | ClinVar |
| 13 | g.32337869T>A | CA387777014 | BRCA2 | c.3514T>A (p.Ser1172Thr) c.3145T>A (p.Ser1049Thr) n.3514T>A | ClinVar dbSNP |
| 13 | g.32337869T>C | CA387777016 | BRCA2 | c.3514T>C (p.Ser1172Pro) c.3145T>C (p.Ser1049Pro) n.3514T>C | dbSNP |
| 13 | g.32337869T>G | CA387777019 | BRCA2 | c.3514T>G (p.Ser1172Ala) c.3145T>G (p.Ser1049Ala) n.3514T>G | ClinVar dbSNP |
| 13 | g.32337869T= | CA2082818012 | BRCA2 | c.3514T= (p.Ser1172=) c.3145T= (p.Ser1049=) n.3514T= | |
| 13 | g.32337870C>A | CA16614291 | BRCA2 | c.3515C>A (p.Ser1172Ter) c.3146C>A (p.Ser1049Ter) n.3515C>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337870C= | CA2082818036 | BRCA2 | c.3515C= (p.Ser1172=) c.3146C= (p.Ser1049=) n.3515C= | |
| 13 | g.32337870C>G | CA018223 | BRCA2 | c.3515C>G (p.Ser1172Trp) c.3146C>G (p.Ser1049Trp) n.3515C>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337870C>T | CA018231 | BRCA2 | c.3515C>T (p.Ser1172Leu) c.3146C>T (p.Ser1049Leu) n.3515C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337871G>A | CA018238 | BRCA2 | c.3516G>A (p.Ser1172=) c.3147G>A (p.Ser1049=) n.3516G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337871G>C | CA483437593 | BRCA2 | c.3516G>C (p.Ser1172=) c.3147G>C (p.Ser1049=) n.3516G>C | dbSNP |
| 13 | g.32337871G= | CA2018046949 | BRCA2 | c.3516G= (p.Ser1172=) c.3147G= (p.Ser1049=) n.3516G= | |
| 13 | g.32337871G>T | CA10579580 | BRCA2 | c.3516G>T (p.Ser1172=) c.3147G>T (p.Ser1049=) n.3516G>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32337872A= | CA2082818055 | BRCA2 | c.3517A= (p.Ile1173=) c.3148A= (p.Ile1050=) n.3517A= | |
| 13 | g.32337872A>C | CA387777030 | BRCA2 | c.3517A>C (p.Ile1173Leu) c.3148A>C (p.Ile1050Leu) n.3517A>C | dbSNP |
| 13 | g.32337872A>G | CA387777031 | BRCA2 | c.3517A>G (p.Ile1173Val) c.3148A>G (p.Ile1050Val) n.3517A>G | ClinVar dbSNP |
| 13 | g.32337872A>T | CA018244 | BRCA2 | c.3517A>T (p.Ile1173Phe) c.3148A>T (p.Ile1050Phe) n.3517A>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |