| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32328077_32337667del | CA2580087045 | BRCA2 | c.632-1366_3312del c.263-1366_2943del n.632-1366_3312del | ClinVar |
| 13 | g.32336269_32337451del | CA2581463478 | BRCA2 | c.1914_3096del (p.Leu639IlefsTer10) c.1545_2727del (p.Leu516IlefsTer10) n.1914_3096del | |
| 13 | g.32337003del | CA10586504 | BRCA2 | c.2648del (p.Phe883SerfsTer12) c.2279del (p.Phe760SerfsTer12) n.2648del | ClinVar dbSNP |
| 13 | g.32337001T>A | CA10587170 | BRCA2 | c.2646T>A (p.Leu882=) c.2277T>A (p.Leu759=) n.2646T>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337001T>C | CA483437021 | BRCA2 | c.2646T>C (p.Leu882=) c.2277T>C (p.Leu759=) n.2646T>C | dbSNP |
| 13 | g.32337001T>G | CA483437022 | BRCA2 | c.2646T>G (p.Leu882=) c.2277T>G (p.Leu759=) n.2646T>G | |
| 13 | g.32337001T= | CA2082810210 | BRCA2 | c.2646T= (p.Leu882=) c.2277T= (p.Leu759=) n.2646T= | |
| 13 | g.32337002T>A | CA387773286 | BRCA2 | c.2647T>A (p.Phe883Ile) c.2278T>A (p.Phe760Ile) n.2647T>A | |
| 13 | g.32337002T>C | CA387773284 | BRCA2 | c.2647T>C (p.Phe883Leu) c.2278T>C (p.Phe760Leu) n.2647T>C | ClinVar |
| 13 | g.32337002T>G | CA387773287 | BRCA2 | c.2647T>G (p.Phe883Val) c.2278T>G (p.Phe760Val) n.2647T>G | |
| 13 | g.32337003T>A | CA387773289 | BRCA2 | c.2648T>A (p.Phe883Tyr) c.2279T>A (p.Phe760Tyr) n.2648T>A | dbSNP |
| 13 | g.32337003T>C | CA387773290 | BRCA2 | c.2648T>C (p.Phe883Ser) c.2279T>C (p.Phe760Ser) n.2648T>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32337003T>G | CA387773292 | BRCA2 | c.2648T>G (p.Phe883Cys) c.2279T>G (p.Phe760Cys) n.2648T>G | |
| 13 | g.32337003T= | CA2082810216 | BRCA2 | c.2648T= (p.Phe883=) c.2279T= (p.Phe760=) n.2648T= | |
| 13 | g.32337003_32337005delinsG | CA2499222112 | BRCA2 | c.2648_2650delinsG (p.Phe883CysfsTer4) c.2279_2281delinsG (p.Phe760CysfsTer4) n.2648_2650delinsG | |
| 13 | g.32337003_32337005delinsCC | CA2582341839 | BRCA2 | c.2648_2650delinsCC (p.Phe883SerfsTer12) c.2279_2281delinsCC (p.Phe760SerfsTer12) n.2648_2650delinsCC | ClinVar |
| 13 | g.32337004C>A | CA387773294 | BRCA2 | c.2649C>A (p.Phe883Leu) c.2280C>A (p.Phe760Leu) n.2649C>A | dbSNP |
| 13 | g.32337004C>G | CA387773296 | BRCA2 | c.2649C>G (p.Phe883Leu) c.2280C>G (p.Phe760Leu) n.2649C>G | dbSNP |
| 13 | g.32337004C>T | CA483437027 | BRCA2 | c.2649C>T (p.Phe883=) c.2280C>T (p.Phe760=) n.2649C>T | dbSNP COSMIC COSMIC |
| 13 | g.32337004_32337005delinsCT | CA2082810224 | BRCA2 | c.2649_2650delinsCT (p.Phe883=) c.2280_2281delinsCT (p.Phe760=) n.2649_2650delinsCT | |
| 13 | g.32337005del | CA10589165 | BRCA2 | c.2650del (p.Ser884GlnfsTer11) c.2281del (p.Ser761GlnfsTer11) n.2650del | ClinVar dbSNP |
| 13 | g.32337005T>A | CA387773302 | BRCA2 | c.2650T>A (p.Ser884Thr) c.2281T>A (p.Ser761Thr) n.2650T>A | dbSNP |
| 13 | g.32337005T>C | CA387773298 | BRCA2 | c.2650T>C (p.Ser884Pro) c.2281T>C (p.Ser761Pro) n.2650T>C | ClinVar dbSNP |
| 13 | g.32337005T>G | CA387773301 | BRCA2 | c.2650T>G (p.Ser884Ala) c.2281T>G (p.Ser761Ala) n.2650T>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337005T= | CA2082810233 | BRCA2 | c.2650T= (p.Ser884=) c.2281T= (p.Ser761=) n.2650T= | |
| 13 | g.32337005_32337009delinsTCAGA | CA2082810232 | BRCA2 | c.2650_2654delinsTCAGA (p.Ser884=) c.2281_2285delinsTCAGA (p.Ser761=) n.2650_2654delinsTCAGA | |
| 13 | g.32337005_32337011delinsC | CA913188617 | BRCA2 | c.2650_2656delinsC (p.Ser884_Asn886delinsHis) c.2281_2287delinsC (p.Ser761_Asn763delinsHis) n.2650_2656delinsC | |
| 13 | g.32337005_32337015del | CA2622601022 | BRCA2 | c.2650_2660del (p.Ser884GlufsTer2) c.2281_2291del (p.Ser761GlufsTer2) n.2650_2660del | ClinVar gnomAD v4 |
| 13 | g.32337006C>A | CA10586505 | BRCA2 | c.2651C>A (p.Ser884Ter) c.2282C>A (p.Ser761Ter) n.2651C>A | ClinVar dbSNP |
| 13 | g.32337006C= | CA2082810257 | BRCA2 | c.2651C= (p.Ser884=) c.2282C= (p.Ser761=) n.2651C= | |
| 13 | g.32337006C>G | CA10579545 | BRCA2 | c.2651C>G (p.Ser884Ter) c.2282C>G (p.Ser761Ter) n.2651C>G | ClinVar dbSNP |
| 13 | g.32337006C>T | CA6940620 | BRCA2 | c.2651C>T (p.Ser884Leu) c.2282C>T (p.Ser761Leu) n.2651C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32337008_32337011del | CA015942 | BRCA2 | c.2653_2656del (p.Asp885MetfsTer9) c.2284_2287del (p.Asp762MetfsTer9) n.2653_2656del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
| 13 | g.32337007A>C | CA483437039 | BRCA2 | c.2652A>C (p.Ser884=) c.2283A>C (p.Ser761=) n.2652A>C | |
| 13 | g.32337007A>G | CA483437040 | BRCA2 | c.2652A>G (p.Ser884=) c.2283A>G (p.Ser761=) n.2652A>G | dbSNP |
| 13 | g.32337007A>T | CA483437042 | BRCA2 | c.2652A>T (p.Ser884=) c.2283A>T (p.Ser761=) n.2652A>T | dbSNP |
| 13 | g.32337008G>A | CA387773308 | BRCA2 | c.2653G>A (p.Asp885Asn) c.2284G>A (p.Asp762Asn) n.2653G>A | dbSNP |
| 13 | g.32337008G>C | CA387773311 | BRCA2 | c.2653G>C (p.Asp885His) c.2284G>C (p.Asp762His) n.2653G>C | dbSNP |
| 13 | g.32337008G>T | CA387773310 | BRCA2 | c.2653G>T (p.Asp885Tyr) c.2284G>T (p.Asp762Tyr) n.2653G>T | dbSNP |
| 13 | g.32337008_32337010delinsGAC | CA2082810273 | BRCA2 | c.2653_2655delinsGAC (p.Asp885=) c.2284_2286delinsGAC (p.Asp762=) n.2653_2655delinsGAC | |
| 13 | g.32337009del | CA483437048 | BRCA2 | c.2654del (p.Asp885AlafsTer10) c.2285del (p.Asp762AlafsTer10) n.2654del | ClinVar dbSNP COSMIC |
| 13 | g.32337009A= | CA2082810287 | BRCA2 | c.2654A= (p.Asp885=) c.2285A= (p.Asp762=) n.2654A= | |
| 13 | g.32337009A>C | CA387773314 | BRCA2 | c.2654A>C (p.Asp885Ala) c.2285A>C (p.Asp762Ala) n.2654A>C | |
| 13 | g.32337009A>G | CA015947 | BRCA2 | c.2654A>G (p.Asp885Gly) c.2285A>G (p.Asp762Gly) n.2654A>G | ClinVar dbSNP |
| 13 | g.32337009A>T | CA387773316 | BRCA2 | c.2654A>T (p.Asp885Val) c.2285A>T (p.Asp762Val) n.2654A>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337010_32337011del | CA6940621 | BRCA2 | c.2655_2656del (p.Asp885GlufsTer2) c.2286_2287del (p.Asp762GlufsTer2) n.2655_2656del | ClinVar dbSNP ExAC gnomAD v2 |
| 13 | g.32337010C>A | CA387773319 | BRCA2 | c.2655C>A (p.Asp885Glu) c.2286C>A (p.Asp762Glu) n.2655C>A | dbSNP |
| 13 | g.32337010C= | CA2082810294 | BRCA2 | c.2655C= (p.Asp885=) c.2286C= (p.Asp762=) n.2655C= | |
| 13 | g.32337010C>G | CA387773321 | BRCA2 | c.2655C>G (p.Asp885Glu) c.2286C>G (p.Asp762Glu) n.2655C>G | dbSNP |
| 13 | g.32337010C>T | CA483437056 | BRCA2 | c.2655C>T (p.Asp885=) c.2286C>T (p.Asp762=) n.2655C>T | ClinVar dbSNP |
| 13 | g.32337010_32337011delinsCA | CA2082810293 | BRCA2 | c.2655_2656delinsCA (p.Asp885=) c.2286_2287delinsCA (p.Asp762=) n.2655_2656delinsCA | |
| 13 | g.32337011A= | CA2082810305 | BRCA2 | c.2656A= (p.Asn886=) c.2287A= (p.Asn763=) n.2656A= | |
| 13 | g.32337011A>C | CA387773323 | BRCA2 | c.2656A>C (p.Asn886His) c.2287A>C (p.Asn763His) n.2656A>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32337011A>G | CA387773325 | BRCA2 | c.2656A>G (p.Asn886Asp) c.2287A>G (p.Asn763Asp) n.2656A>G | ClinVar |
| 13 | g.32337011A>T | CA387773326 | BRCA2 | c.2656A>T (p.Asn886Tyr) c.2287A>T (p.Asn763Tyr) n.2656A>T | dbSNP |
| 13 | g.32337011_32337012del | CA2581463423 | BRCA2 | c.2656_2657del (p.Asn886Ter) c.2287_2288del (p.Asn763Ter) n.2656_2657del | |
| 13 | g.32337012del | CA10589166 | BRCA2 | c.2657del (p.Asn886MetfsTer9) c.2288del (p.Asn763MetfsTer9) n.2657del | ClinVar dbSNP |
| 13 | g.32337012A= | CA2082810312 | BRCA2 | c.2657A= (p.Asn886=) c.2288A= (p.Asn763=) n.2657A= | |
| 13 | g.32337012A>C | CA387773328 | BRCA2 | c.2657A>C (p.Asn886Thr) c.2288A>C (p.Asn763Thr) n.2657A>C | |
| 13 | g.32337012A>G | CA015957 | BRCA2 | c.2657A>G (p.Asn886Ser) c.2288A>G (p.Asn763Ser) n.2657A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32337012A>T | CA015961 | BRCA2 | c.2657A>T (p.Asn886Ile) c.2288A>T (p.Asn763Ile) n.2657A>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337012_32337014delinsATG | CA2082810311 | BRCA2 | c.2657_2659delinsATG (p.Asn886=) c.2288_2290delinsATG (p.Asn763=) n.2657_2659delinsATG | |
| 13 | g.32337013T>A | CA387773332 | BRCA2 | c.2658T>A (p.Asn886Lys) c.2289T>A (p.Asn763Lys) n.2658T>A | dbSNP |
| 13 | g.32337013T>C | CA483437071 | BRCA2 | c.2658T>C (p.Asn886=) c.2289T>C (p.Asn763=) n.2658T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337013T>G | CA387773333 | BRCA2 | c.2658T>G (p.Asn886Lys) c.2289T>G (p.Asn763Lys) n.2658T>G | gnomAD v4 |
| 13 | g.32337013T= | CA2082810338 | BRCA2 | c.2658T= (p.Asn886=) c.2289T= (p.Asn763=) n.2658T= | |
| 13 | g.32337013_32337014del | CA015970 | BRCA2 | c.2658_2659del (p.Asn886LysfsTer3) c.2289_2290del (p.Asn763LysfsTer3) n.2658_2659del | ClinVar dbSNP |
| 13 | g.32337013_32337014dup | CA6940622 | BRCA2 | c.2658_2659dup (p.Glu887ValfsTer9) c.2289_2290dup (p.Glu764ValfsTer9) n.2658_2659dup | ClinVar dbSNP ExAC gnomAD v2 |
| 13 | g.32337014G>A | CA10579546 | BRCA2 | c.2659G>A (p.Glu887Lys) c.2290G>A (p.Glu764Lys) n.2659G>A | ClinVar dbSNP |
| 13 | g.32337014G>C | CA387773337 | BRCA2 | c.2659G>C (p.Glu887Gln) c.2290G>C (p.Glu764Gln) n.2659G>C | |
| 13 | g.32337014G= | CA2082810347 | BRCA2 | c.2659G= (p.Glu887=) c.2290G= (p.Glu764=) n.2659G= | |
| 13 | g.32337014G>T | CA387773336 | BRCA2 | c.2659G>T (p.Glu887Ter) c.2290G>T (p.Glu764Ter) n.2659G>T | |
| 13 | g.32337015A= | CA2082810356 | BRCA2 | c.2660A= (p.Glu887=) c.2291A= (p.Glu764=) n.2660A= | |
| 13 | g.32337015A>C | CA387773339 | BRCA2 | c.2660A>C (p.Glu887Ala) c.2291A>C (p.Glu764Ala) n.2660A>C | |
| 13 | g.32337015A>G | CA015980 | BRCA2 | c.2660A>G (p.Glu887Gly) c.2291A>G (p.Glu764Gly) n.2660A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337015A>T | CA387773342 | BRCA2 | c.2660A>T (p.Glu887Val) c.2291A>T (p.Glu764Val) n.2660A>T | dbSNP |
| 13 | g.32337016G>A | CA10579547 | BRCA2 | c.2661G>A (p.Glu887=) c.2292G>A (p.Glu764=) n.2661G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32337016G>C | CA16614255 | BRCA2 | c.2661G>C (p.Glu887Asp) c.2292G>C (p.Glu764Asp) n.2661G>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337016G= | CA2082810364 | BRCA2 | c.2661G= (p.Glu887=) c.2292G= (p.Glu764=) n.2661G= | |
| 13 | g.32337016G>T | CA387773345 | BRCA2 | c.2661G>T (p.Glu887Asp) c.2292G>T (p.Glu764Asp) n.2661G>T | dbSNP |
| 13 | g.32337017A>C | CA387773347 | BRCA2 | c.2662A>C (p.Asn888His) c.2293A>C (p.Asn765His) n.2662A>C | |
| 13 | g.32337017A>G | CA387773350 | BRCA2 | c.2662A>G (p.Asn888Asp) c.2293A>G (p.Asn765Asp) n.2662A>G | |
| 13 | g.32337017A>T | CA387773349 | BRCA2 | c.2662A>T (p.Asn888Tyr) c.2293A>T (p.Asn765Tyr) n.2662A>T | dbSNP |
| 13 | g.32337018A= | CA2082810379 | BRCA2 | c.2663A= (p.Asn888=) c.2294A= (p.Asn765=) n.2663A= | |
| 13 | g.32337018A>C | CA387773352 | BRCA2 | c.2663A>C (p.Asn888Thr) c.2294A>C (p.Asn765Thr) n.2663A>C | |
| 13 | g.32337018A>G | CA387773353 | BRCA2 | c.2663A>G (p.Asn888Ser) c.2294A>G (p.Asn765Ser) n.2663A>G | ClinVar dbSNP |
| 13 | g.32337018A>T | CA387773354 | BRCA2 | c.2663A>T (p.Asn888Ile) c.2294A>T (p.Asn765Ile) n.2663A>T | dbSNP |
| 13 | g.32337019T>A | CA387773356 | BRCA2 | c.2664T>A (p.Asn888Lys) c.2295T>A (p.Asn765Lys) n.2664T>A | |
| 13 | g.32337019T>C | CA483437087 | BRCA2 | c.2664T>C (p.Asn888=) c.2295T>C (p.Asn765=) n.2664T>C | ClinVar dbSNP |
| 13 | g.32337019T>G | CA387773358 | BRCA2 | c.2664T>G (p.Asn888Lys) c.2295T>G (p.Asn765Lys) n.2664T>G | |
| 13 | g.32337020A= | CA2082810384 | BRCA2 | c.2665A= (p.Asn889=) c.2296A= (p.Asn766=) n.2665A= | |
| 13 | g.32337020A>C | CA387773359 | BRCA2 | c.2665A>C (p.Asn889His) c.2296A>C (p.Asn766His) n.2665A>C | |
| 13 | g.32337020A>G | CA16619675 | BRCA2 | c.2665A>G (p.Asn889Asp) c.2296A>G (p.Asn766Asp) n.2665A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32337020A>T | CA387773361 | BRCA2 | c.2665A>T (p.Asn889Tyr) c.2296A>T (p.Asn766Tyr) n.2665A>T | dbSNP |
| 13 | g.32337021del | CA2695218013 | BRCA2 | c.2666del (p.Asn889IlefsTer6) c.2297del (p.Asn766IlefsTer6) n.2666del | ClinVar |
| 13 | g.32337021A= | CA2082810387 | BRCA2 | c.2666A= (p.Asn889=) c.2297A= (p.Asn766=) n.2666A= | |
| 13 | g.32337021A>C | CA387773362 | BRCA2 | c.2666A>C (p.Asn889Thr) c.2297A>C (p.Asn766Thr) n.2666A>C | |
| 13 | g.32337021A>G | CA387773363 | BRCA2 | c.2666A>G (p.Asn889Ser) c.2297A>G (p.Asn766Ser) n.2666A>G | ClinVar dbSNP |
| 13 | g.32337021A>T | CA387773365 | BRCA2 | c.2666A>T (p.Asn889Ile) c.2297A>T (p.Asn766Ile) n.2666A>T | |
| 13 | g.32337021_32337022delinsAT | CA2082810390 | BRCA2 | c.2666_2667delinsAT (p.Asn889=) c.2297_2298delinsAT (p.Asn766=) n.2666_2667delinsAT | |
| 13 | g.32337021_32337022insC | CA2739277503 | BRCA2 | c.2666_2667insC (p.Val891CysfsTer6) c.2297_2298insC (p.Val768CysfsTer6) n.2666_2667insC | ClinVar |
| 13 | g.32337022T>A | CA387773367 | BRCA2 | c.2667T>A (p.Asn889Lys) c.2298T>A (p.Asn766Lys) n.2667T>A | dbSNP |
| 13 | g.32337022T>C | CA015988 | BRCA2 | c.2667T>C (p.Asn889=) c.2298T>C (p.Asn766=) n.2667T>C | ClinVar dbSNP |
| 13 | g.32337022T>G | CA387773369 | BRCA2 | c.2667T>G (p.Asn889Lys) c.2298T>G (p.Asn766Lys) n.2667T>G | dbSNP |
| 13 | g.32337022T= | CA2082810395 | BRCA2 | c.2667T= (p.Asn889=) c.2298T= (p.Asn766=) n.2667T= | |
| 13 | g.32337025dup | CA2727873213 | BRCA2 | c.2670dup (p.Val891CysfsTer6) c.2301dup (p.Val768CysfsTer6) n.2670dup | dbSNP |
| 13 | g.32337025del | CA658653669 | BRCA2 | c.2670del (p.Phe890LeufsTer5) c.2301del (p.Phe767LeufsTer5) n.2670del | ClinVar dbSNP |
| 13 | g.32337023T>A | CA387773371 | BRCA2 | c.2668T>A (p.Phe890Ile) c.2299T>A (p.Phe767Ile) n.2668T>A | dbSNP |
| 13 | g.32337023T>C | CA387773373 | BRCA2 | c.2668T>C (p.Phe890Leu) c.2299T>C (p.Phe767Leu) n.2668T>C | dbSNP |
| 13 | g.32337023T>G | CA387773374 | BRCA2 | c.2668T>G (p.Phe890Val) c.2299T>G (p.Phe767Val) n.2668T>G | |
| 13 | g.32337023T= | CA2082810404 | BRCA2 | c.2668T= (p.Phe890=) c.2299T= (p.Phe767=) n.2668T= | |
| 13 | g.32337024T>A | CA387773376 | BRCA2 | c.2669T>A (p.Phe890Tyr) c.2300T>A (p.Phe767Tyr) n.2669T>A | |
| 13 | g.32337024T>C | CA387773377 | BRCA2 | c.2669T>C (p.Phe890Ser) c.2300T>C (p.Phe767Ser) n.2669T>C | |
| 13 | g.32337024T>G | CA387773379 | BRCA2 | c.2669T>G (p.Phe890Cys) c.2300T>G (p.Phe767Cys) n.2669T>G | ClinVar |
| 13 | g.32337025T>A | CA387773380 | BRCA2 | c.2670T>A (p.Phe890Leu) c.2301T>A (p.Phe767Leu) n.2670T>A | dbSNP COSMIC COSMIC |
| 13 | g.32337025T>C | CA483437111 | BRCA2 | c.2670T>C (p.Phe890=) c.2301T>C (p.Phe767=) n.2670T>C | |
| 13 | g.32337025T>G | CA387773382 | BRCA2 | c.2670T>G (p.Phe890Leu) c.2301T>G (p.Phe767Leu) n.2670T>G | |
| 13 | g.32337026G>A | CA387773384 | BRCA2 | c.2671G>A (p.Val891Ile) c.2302G>A (p.Val768Ile) n.2671G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337026G>C | CA337799 | BRCA2 | c.2671G>C (p.Val891Leu) c.2302G>C (p.Val768Leu) n.2671G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32337026G= | CA2082810414 | BRCA2 | c.2671G= (p.Val891=) c.2302G= (p.Val768=) n.2671G= | |
| 13 | g.32337026G>T | CA387773386 | BRCA2 | c.2671G>T (p.Val891Phe) c.2302G>T (p.Val768Phe) n.2671G>T | dbSNP |
| 13 | g.32337027T>A | CA387773391 | BRCA2 | c.2672T>A (p.Val891Asp) c.2303T>A (p.Val768Asp) n.2672T>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337027T>C | CA387773390 | BRCA2 | c.2672T>C (p.Val891Ala) c.2303T>C (p.Val768Ala) n.2672T>C | ClinVar dbSNP |
| 13 | g.32337027T>G | CA387773388 | BRCA2 | c.2672T>G (p.Val891Gly) c.2303T>G (p.Val768Gly) n.2672T>G | |
| 13 | g.32337027T= | CA2082810426 | BRCA2 | c.2672T= (p.Val891=) c.2303T= (p.Val768=) n.2672T= | |
| 13 | g.32337027dup | CA1139663119 | BRCA2 | c.2672dup (p.Phe892LeufsTer5) c.2303dup (p.Phe769LeufsTer5) n.2672dup | ClinVar dbSNP |
| 13 | g.32337028C>A | CA483437116 | BRCA2 | c.2673C>A (p.Val891=) c.2304C>A (p.Val768=) n.2673C>A | dbSNP |
| 13 | g.32337028C>G | CA483437118 | BRCA2 | c.2673C>G (p.Val891=) c.2304C>G (p.Val768=) n.2673C>G | ClinVar dbSNP |
| 13 | g.32337028C>T | CA483437126 | BRCA2 | c.2673C>T (p.Val891=) c.2304C>T (p.Val768=) n.2673C>T | dbSNP |
| 13 | g.32337029T>A | CA387773393 | BRCA2 | c.2674T>A (p.Phe892Ile) c.2305T>A (p.Phe769Ile) n.2674T>A | dbSNP |
| 13 | g.32337029T>C | CA387773394 | BRCA2 | c.2674T>C (p.Phe892Leu) c.2305T>C (p.Phe769Leu) n.2674T>C | ClinVar dbSNP |
| 13 | g.32337029T>G | CA387773396 | BRCA2 | c.2674T>G (p.Phe892Val) c.2305T>G (p.Phe769Val) n.2674T>G | |
| 13 | g.32337029T= | CA2082810434 | BRCA2 | c.2674T= (p.Phe892=) c.2305T= (p.Phe769=) n.2674T= | |
| 13 | g.32337030T>A | CA387773397 | BRCA2 | c.2675T>A (p.Phe892Tyr) c.2306T>A (p.Phe769Tyr) n.2675T>A | dbSNP |
| 13 | g.32337030T>C | CA387773399 | BRCA2 | c.2675T>C (p.Phe892Ser) c.2306T>C (p.Phe769Ser) n.2675T>C | ClinVar |
| 13 | g.32337030T>G | CA387773401 | BRCA2 | c.2675T>G (p.Phe892Cys) c.2306T>G (p.Phe769Cys) n.2675T>G | |
| 13 | g.32337030_32337031delinsTC | CA2082810438 | BRCA2 | c.2675_2676delinsTC (p.Phe892=) c.2306_2307delinsTC (p.Phe769=) n.2675_2676delinsTC | |
| 13 | g.32337031C>A | CA016006 | BRCA2 | c.2676C>A (p.Phe892Leu) c.2307C>A (p.Phe769Leu) n.2676C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32337031C= | CA2082810448 | BRCA2 | c.2676C= (p.Phe892=) c.2307C= (p.Phe769=) n.2676C= | |
| 13 | g.32337031C>G | CA387773403 | BRCA2 | c.2676C>G (p.Phe892Leu) c.2307C>G (p.Phe769Leu) n.2676C>G | dbSNP |
| 13 | g.32337031C>T | CA483437134 | BRCA2 | c.2676C>T (p.Phe892=) c.2307C>T (p.Phe769=) n.2676C>T | dbSNP |
| 13 | g.32337031_32337032del | CA2499222113 | BRCA2 | c.2676_2677del (p.Phe892LeufsTer4) c.2307_2308del (p.Phe769LeufsTer4) n.2676_2677del | ClinVar dbSNP |
| 13 | g.32337032del | CA10584441 | BRCA2 | c.2677del (p.Gln893LysfsTer2) c.2308del (p.Gln770LysfsTer2) n.2677del | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32337032C>A | CA387773406 | BRCA2 | c.2677C>A (p.Gln893Lys) c.2308C>A (p.Gln770Lys) n.2677C>A | dbSNP |
| 13 | g.32337032C= | CA2082810452 | BRCA2 | c.2677C= (p.Gln893=) c.2308C= (p.Gln770=) n.2677C= | |
| 13 | g.32337032C>G | CA387773408 | BRCA2 | c.2677C>G (p.Gln893Glu) c.2308C>G (p.Gln770Glu) n.2677C>G | dbSNP |
| 13 | g.32337032C>T | CA387773409 | BRCA2 | c.2677C>T (p.Gln893Ter) c.2308C>T (p.Gln770Ter) n.2677C>T | ClinVar dbSNP |
| 13 | g.32337033A= | CA2082810460 | BRCA2 | c.2678A= (p.Gln893=) c.2309A= (p.Gln770=) n.2678A= | |
| 13 | g.32337033A>C | CA387773414 | BRCA2 | c.2678A>C (p.Gln893Pro) c.2309A>C (p.Gln770Pro) n.2678A>C | |
| 13 | g.32337033A>G | CA016015 | BRCA2 | c.2678A>G (p.Gln893Arg) c.2309A>G (p.Gln770Arg) n.2678A>G | ClinVar dbSNP |
| 13 | g.32337033A>T | CA387773412 | BRCA2 | c.2678A>T (p.Gln893Leu) c.2309A>T (p.Gln770Leu) n.2678A>T | dbSNP |
| 13 | g.32337034A= | CA2082810464 | BRCA2 | c.2679A= (p.Gln893=) c.2310A= (p.Gln770=) n.2679A= | |
| 13 | g.32337034A>C | CA387773415 | BRCA2 | c.2679A>C (p.Gln893His) c.2310A>C (p.Gln770His) n.2679A>C | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32337034A>G | CA016024 | BRCA2 | c.2679A>G (p.Gln893=) c.2310A>G (p.Gln770=) n.2679A>G | ClinVar dbSNP |
| 13 | g.32337034A>T | CA387773417 | BRCA2 | c.2679A>T (p.Gln893His) c.2310A>T (p.Gln770His) n.2679A>T | dbSNP |
| 13 | g.32337035del | CA2695218015 | BRCA2 | c.2680del (p.Val894Ter) c.2311del (p.Val771Ter) n.2680del | |
| 13 | g.32337035G>A | CA016044 | BRCA2 | c.2680G>A (p.Val894Ile) c.2311G>A (p.Val771Ile) n.2680G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337035G>C | CA387773420 | BRCA2 | c.2680G>C (p.Val894Leu) c.2311G>C (p.Val771Leu) n.2680G>C | ClinVar dbSNP |
| 13 | g.32337035G= | CA2082810466 | BRCA2 | c.2680G= (p.Val894=) c.2311G= (p.Val771=) n.2680G= | |
| 13 | g.32337035G>T | CA387773421 | BRCA2 | c.2680G>T (p.Val894Leu) c.2311G>T (p.Val771Leu) n.2680G>T | ClinVar gnomAD v4 |
| 13 | g.32337036T>A | CA387773424 | BRCA2 | c.2681T>A (p.Val894Glu) c.2312T>A (p.Val771Glu) n.2681T>A | dbSNP |
| 13 | g.32337036T>C | CA387773425 | BRCA2 | c.2681T>C (p.Val894Ala) c.2312T>C (p.Val771Ala) n.2681T>C | dbSNP |
| 13 | g.32337036T>G | CA387773427 | BRCA2 | c.2681T>G (p.Val894Gly) c.2312T>G (p.Val771Gly) n.2681T>G | dbSNP |
| 13 | g.32337036dup | CA2580087295 | BRCA2 | c.2681dup (p.Ala895SerfsTer2) c.2312dup (p.Ala772SerfsTer2) n.2681dup | ClinVar |
| 13 | g.32337036_32337037delinsAG | CA16619676 | BRCA2 | c.2681_2682delinsAG (p.Val894Glu) c.2312_2313delinsAG (p.Val771Glu) n.2681_2682delinsAG | ClinVar dbSNP |
| 13 | g.32337036_32337037delinsTA | CA2082810469 | BRCA2 | c.2681_2682delinsTA (p.Val894=) c.2312_2313delinsTA (p.Val771=) n.2681_2682delinsTA | |
| 13 | g.32337037A>C | CA483437146 | BRCA2 | c.2682A>C (p.Val894=) c.2313A>C (p.Val771=) n.2682A>C | ClinVar dbSNP |
| 13 | g.32337037A>G | CA483437147 | BRCA2 | c.2682A>G (p.Val894=) c.2313A>G (p.Val771=) n.2682A>G | dbSNP |
| 13 | g.32337037A>T | CA483437155 | BRCA2 | c.2682A>T (p.Val894=) c.2313A>T (p.Val771=) n.2682A>T | ClinVar dbSNP |
| 13 | g.32337038G>A | CA016049 | BRCA2 | c.2683G>A (p.Ala895Thr) c.2314G>A (p.Ala772Thr) n.2683G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337038G>C | CA387773429 | BRCA2 | c.2683G>C (p.Ala895Pro) c.2314G>C (p.Ala772Pro) n.2683G>C | dbSNP |
| 13 | g.32337038G= | CA2082810481 | BRCA2 | c.2683G= (p.Ala895=) c.2314G= (p.Ala772=) n.2683G= | |
| 13 | g.32337038G>T | CA016058 | BRCA2 | c.2683G>T (p.Ala895Ser) c.2314G>T (p.Ala772Ser) n.2683G>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337038_32337039delinsGC | CA2082810483 | BRCA2 | c.2683_2684delinsGC (p.Ala895=) c.2314_2315delinsGC (p.Ala772=) n.2683_2684delinsGC | |
| 13 | g.32337039del | CA016067 | BRCA2 | c.2684del (p.Ala895ValfsTer9) c.2315del (p.Ala772ValfsTer9) n.2684del | ClinVar dbSNP |
| 13 | g.32337039C>A | CA387773432 | BRCA2 | c.2684C>A (p.Ala895Asp) c.2315C>A (p.Ala772Asp) n.2684C>A | dbSNP |
| 13 | g.32337039C>G | CA387773434 | BRCA2 | c.2684C>G (p.Ala895Gly) c.2315C>G (p.Ala772Gly) n.2684C>G | dbSNP |
| 13 | g.32337039C>T | CA387773435 | BRCA2 | c.2684C>T (p.Ala895Val) c.2315C>T (p.Ala772Val) n.2684C>T | dbSNP |
| 13 | g.32337040T>A | CA483437159 | BRCA2 | c.2685T>A (p.Ala895=) c.2316T>A (p.Ala772=) n.2685T>A | |
| 13 | g.32337040T>C | CA483437162 | BRCA2 | c.2685T>C (p.Ala895=) c.2316T>C (p.Ala772=) n.2685T>C | gnomAD v4 |
| 13 | g.32337040T>G | CA483437161 | BRCA2 | c.2685T>G (p.Ala895=) c.2316T>G (p.Ala772=) n.2685T>G | ClinVar dbSNP |
| 13 | g.32337040T= | CA2082810498 | BRCA2 | c.2685T= (p.Ala895=) c.2316T= (p.Ala772=) n.2685T= | |
| 13 | g.32337041A= | CA2082810505 | BRCA2 | c.2686A= (p.Asn896=) c.2317A= (p.Asn773=) n.2686A= | |
| 13 | g.32337041A>C | CA387773440 | BRCA2 | c.2686A>C (p.Asn896His) c.2317A>C (p.Asn773His) n.2686A>C | |
| 13 | g.32337041A>G | CA387773438 | BRCA2 | c.2686A>G (p.Asn896Asp) c.2317A>G (p.Asn773Asp) n.2686A>G | dbSNP |
| 13 | g.32337041A>T | CA387773439 | BRCA2 | c.2686A>T (p.Asn896Tyr) c.2317A>T (p.Asn773Tyr) n.2686A>T | dbSNP |
| 13 | g.32337042A= | CA2082810520 | BRCA2 | c.2687A= (p.Asn896=) c.2318A= (p.Asn773=) n.2687A= | |
| 13 | g.32337042A>C | CA387773441 | BRCA2 | c.2687A>C (p.Asn896Thr) c.2318A>C (p.Asn773Thr) n.2687A>C | |
| 13 | g.32337042A>G | CA387773442 | BRCA2 | c.2687A>G (p.Asn896Ser) c.2318A>G (p.Asn773Ser) n.2687A>G | ClinVar |
| 13 | g.32337042A>T | CA387773444 | BRCA2 | c.2687A>T (p.Asn896Ile) c.2318A>T (p.Asn773Ile) n.2687A>T | ClinVar dbSNP |
| 13 | g.32337042_32337043insGA | CA658683842 | BRCA2 | c.2687_2688insGA (p.Asn896LysfsTer9) c.2318_2319insGA (p.Asn773LysfsTer9) n.2687_2688insGA | ClinVar dbSNP |
| 13 | g.32337043T>A | CA387773446 | BRCA2 | c.2688T>A (p.Asn896Lys) c.2319T>A (p.Asn773Lys) n.2688T>A | dbSNP |
| 13 | g.32337043T>C | CA6940623 | BRCA2 | c.2688T>C (p.Asn896=) c.2319T>C (p.Asn773=) n.2688T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32337043T>G | CA387773448 | BRCA2 | c.2688T>G (p.Asn896Lys) c.2319T>G (p.Asn773Lys) n.2688T>G | ClinVar dbSNP |
| 13 | g.32337043T= | CA2082810531 | BRCA2 | c.2688T= (p.Asn896=) c.2319T= (p.Asn773=) n.2688T= | |
| 13 | g.32337043_32337048delinsTGAAAG | CA2082810528 | BRCA2 | c.2688_2693delinsTGAAAG (p.Asn896=) c.2319_2324delinsTGAAAG (p.Asn773=) n.2688_2693delinsTGAAAG | |
| 13 | g.32337044G>A | CA247502815 | BRCA2 | c.2689G>A (p.Glu897Lys) c.2320G>A (p.Glu774Lys) n.2689G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337044G>C | CA387773452 | BRCA2 | c.2689G>C (p.Glu897Gln) c.2320G>C (p.Glu774Gln) n.2689G>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337044G= | CA2082810554 | BRCA2 | c.2689G= (p.Glu897=) c.2320G= (p.Glu774=) n.2689G= | |
| 13 | g.32337044G>T | CA387773453 | BRCA2 | c.2689G>T (p.Glu897Ter) c.2320G>T (p.Glu774Ter) n.2689G>T | ClinVar dbSNP COSMIC COSMIC |
| 13 | g.32337047_32337051del | CA016075 | BRCA2 | c.2692_2696del (p.Arg898Ter) c.2323_2327del (p.Arg775Ter) n.2692_2696del | ClinVar dbSNP |
| 13 | g.32337045A>C | CA387773455 | BRCA2 | c.2690A>C (p.Glu897Ala) c.2321A>C (p.Glu774Ala) n.2690A>C | |
| 13 | g.32337045A>G | CA387773456 | BRCA2 | c.2690A>G (p.Glu897Gly) c.2321A>G (p.Glu774Gly) n.2690A>G | ClinVar |
| 13 | g.32337045A>T | CA387773458 | BRCA2 | c.2690A>T (p.Glu897Val) c.2321A>T (p.Glu774Val) n.2690A>T | dbSNP |
| 13 | g.32337046A= | CA2082810564 | BRCA2 | c.2691A= (p.Glu897=) c.2322A= (p.Glu774=) n.2691A= | |
| 13 | g.32337046A>C | CA387773460 | BRCA2 | c.2691A>C (p.Glu897Asp) c.2322A>C (p.Glu774Asp) n.2691A>C | |
| 13 | g.32337046A>G | CA483437182 | BRCA2 | c.2691A>G (p.Glu897=) c.2322A>G (p.Glu774=) n.2691A>G | ClinVar dbSNP |
| 13 | g.32337046A>T | CA387773459 | BRCA2 | c.2691A>T (p.Glu897Asp) c.2322A>T (p.Glu774Asp) n.2691A>T | |
| 13 | g.32337047A= | CA2082810570 | BRCA2 | c.2692A= (p.Arg898=) c.2323A= (p.Arg775=) n.2692A= | |
| 13 | g.32337047A>C | CA483437183 | BRCA2 | c.2692A>C (p.Arg898=) c.2323A>C (p.Arg775=) n.2692A>C | |
| 13 | g.32337047A>G | CA387773464 | BRCA2 | c.2692A>G (p.Arg898Gly) c.2323A>G (p.Arg775Gly) n.2692A>G | ClinVar dbSNP |
| 13 | g.32337047A>T | CA387773463 | BRCA2 | c.2692A>T (p.Arg898Trp) c.2323A>T (p.Arg775Trp) n.2692A>T | dbSNP |
| 13 | g.32337048G>A | CA387773466 | BRCA2 | c.2693G>A (p.Arg898Lys) c.2324G>A (p.Arg775Lys) n.2693G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337048G>C | CA016082 | BRCA2 | c.2693G>C (p.Arg898Thr) c.2324G>C (p.Arg775Thr) n.2693G>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32337048G= | CA2082810580 | BRCA2 | c.2693G= (p.Arg898=) c.2324G= (p.Arg775=) n.2693G= | |
| 13 | g.32337048G>T | CA387773468 | BRCA2 | c.2693G>T (p.Arg898Met) c.2324G>T (p.Arg775Met) n.2693G>T | dbSNP |
| 13 | g.32337049G>A | CA483437190 | BRCA2 | c.2694G>A (p.Arg898=) c.2325G>A (p.Arg775=) n.2694G>A | dbSNP |
| 13 | g.32337049G>C | CA387773470 | BRCA2 | c.2694G>C (p.Arg898Ser) c.2325G>C (p.Arg775Ser) n.2694G>C | dbSNP |
| 13 | g.32337049G= | CA2082810587 | BRCA2 | c.2694G= (p.Arg898=) c.2325G= (p.Arg775=) n.2694G= | |
| 13 | g.32337049G>T | CA387773472 | BRCA2 | c.2694G>T (p.Arg898Ser) c.2325G>T (p.Arg775Ser) n.2694G>T | ClinVar dbSNP |
| 13 | g.32337050A= | CA2082810596 | BRCA2 | c.2695A= (p.Asn899=) c.2326A= (p.Asn776=) n.2695A= | |
| 13 | g.32337050A>C | CA387773474 | BRCA2 | c.2695A>C (p.Asn899His) c.2326A>C (p.Asn776His) n.2695A>C | |
| 13 | g.32337050A>G | CA6940624 | BRCA2 | c.2695A>G (p.Asn899Asp) c.2326A>G (p.Asn776Asp) n.2695A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337050A>T | CA387773476 | BRCA2 | c.2695A>T (p.Asn899Tyr) c.2326A>T (p.Asn776Tyr) n.2695A>T | |
| 13 | g.32337051A= | CA2082810603 | BRCA2 | c.2696A= (p.Asn899=) c.2327A= (p.Asn776=) n.2696A= | |
| 13 | g.32337051A>C | CA387773477 | BRCA2 | c.2696A>C (p.Asn899Thr) c.2327A>C (p.Asn776Thr) n.2696A>C | |
| 13 | g.32337051A>G | CA387773479 | BRCA2 | c.2696A>G (p.Asn899Ser) c.2327A>G (p.Asn776Ser) n.2696A>G | ClinVar dbSNP |
| 13 | g.32337051A>T | CA387773480 | BRCA2 | c.2696A>T (p.Asn899Ile) c.2327A>T (p.Asn776Ile) n.2696A>T | |
| 13 | g.32337052T>A | CA387773484 | BRCA2 | c.2697T>A (p.Asn899Lys) c.2328T>A (p.Asn776Lys) n.2697T>A | dbSNP |
| 13 | g.32337052T>C | CA483437195 | BRCA2 | c.2697T>C (p.Asn899=) c.2328T>C (p.Asn776=) n.2697T>C | dbSNP |
| 13 | g.32337052T>G | CA387773482 | BRCA2 | c.2697T>G (p.Asn899Lys) c.2328T>G (p.Asn776Lys) n.2697T>G | dbSNP |
| 13 | g.32337053A= | CA2082810610 | BRCA2 | c.2698A= (p.Asn900=) c.2329A= (p.Asn777=) n.2698A= | |
| 13 | g.32337053A>C | CA387773485 | BRCA2 | c.2698A>C (p.Asn900His) c.2329A>C (p.Asn777His) n.2698A>C | ClinVar dbSNP |
| 13 | g.32337053A>G | CA016090 | BRCA2 | c.2698A>G (p.Asn900Asp) c.2329A>G (p.Asn777Asp) n.2698A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337053A>T | CA387773487 | BRCA2 | c.2698A>T (p.Asn900Tyr) c.2329A>T (p.Asn777Tyr) n.2698A>T | dbSNP |
| 13 | g.32337054del | CA2695218016 | BRCA2 | c.2699del (p.Asn900IlefsTer4) c.2330del (p.Asn777IlefsTer4) n.2699del | |
| 13 | g.32337054A= | CA2082810619 | BRCA2 | c.2699A= (p.Asn900=) c.2330A= (p.Asn777=) n.2699A= | |
| 13 | g.32337054A>C | CA387773489 | BRCA2 | c.2699A>C (p.Asn900Thr) c.2330A>C (p.Asn777Thr) n.2699A>C | ClinVar dbSNP |
| 13 | g.32337054A>G | CA387773491 | BRCA2 | c.2699A>G (p.Asn900Ser) c.2330A>G (p.Asn777Ser) n.2699A>G | dbSNP |
| 13 | g.32337054A>T | CA387773493 | BRCA2 | c.2699A>T (p.Asn900Ile) c.2330A>T (p.Asn777Ile) n.2699A>T | dbSNP COSMIC |
| 13 | g.32337055T>A | CA387773494 | BRCA2 | c.2700T>A (p.Asn900Lys) c.2331T>A (p.Asn777Lys) n.2700T>A | dbSNP |
| 13 | g.32337055T>C | CA483437198 | BRCA2 | c.2700T>C (p.Asn900=) c.2331T>C (p.Asn777=) n.2700T>C | ClinVar dbSNP |
| 13 | g.32337055T>G | CA387773496 | BRCA2 | c.2700T>G (p.Asn900Lys) c.2331T>G (p.Asn777Lys) n.2700T>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337055T= | CA2082810632 | BRCA2 | c.2700T= (p.Asn900=) c.2331T= (p.Asn777=) n.2700T= | |
| 13 | g.32337055_32337056delinsTC | CA2082810629 | BRCA2 | c.2700_2701delinsTC (p.Asn900=) c.2331_2332delinsTC (p.Asn777=) n.2700_2701delinsTC | |
| 13 | g.32337056del | CA016132 | BRCA2 | c.2701del (p.Ala902LeufsTer2) c.2332del (p.Ala779LeufsTer2) n.2701del | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337056C>A | CA387773498 | BRCA2 | c.2701C>A (p.Leu901Ile) c.2332C>A (p.Leu778Ile) n.2701C>A | ClinVar dbSNP COSMIC COSMIC |
| 13 | g.32337056C= | CA2082810651 | BRCA2 | c.2701C= (p.Leu901=) c.2332C= (p.Leu778=) n.2701C= | |
| 13 | g.32337056C>G | CA387773499 | BRCA2 | c.2701C>G (p.Leu901Val) c.2332C>G (p.Leu778Val) n.2701C>G | ClinVar dbSNP |
| 13 | g.32337056C>T | CA387773501 | BRCA2 | c.2701C>T (p.Leu901Phe) c.2332C>T (p.Leu778Phe) n.2701C>T | dbSNP |
| 13 | g.32337056_32337057delinsCT | CA2082810643 | BRCA2 | c.2701_2702delinsCT (p.Leu901=) c.2332_2333delinsCT (p.Leu778=) n.2701_2702delinsCT | |
| 13 | g.32337057T>A | CA387773508 | BRCA2 | c.2702T>A (p.Leu901His) c.2333T>A (p.Leu778His) n.2702T>A | dbSNP |
| 13 | g.32337057T>C | CA387773506 | BRCA2 | c.2702T>C (p.Leu901Pro) c.2333T>C (p.Leu778Pro) n.2702T>C | ClinVar gnomAD v4 |
| 13 | g.32337057T>G | CA387773505 | BRCA2 | c.2702T>G (p.Leu901Arg) c.2333T>G (p.Leu778Arg) n.2702T>G | |
| 13 | g.32337058del | CA10589167 | BRCA2 | c.2703del (p.Ala902LeufsTer2) c.2334del (p.Ala779LeufsTer2) n.2703del | ClinVar dbSNP |
| 13 | g.32337058T>A | CA016141 | BRCA2 | c.2703T>A (p.Leu901=) c.2334T>A (p.Leu778=) n.2703T>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337058T>C | CA483437200 | BRCA2 | c.2703T>C (p.Leu901=) c.2334T>C (p.Leu778=) n.2703T>C | ClinVar dbSNP |
| 13 | g.32337058T>G | CA483437201 | BRCA2 | c.2703T>G (p.Leu901=) c.2334T>G (p.Leu778=) n.2703T>G | |
| 13 | g.32337058T= | CA2082810675 | BRCA2 | c.2703T= (p.Leu901=) c.2334T= (p.Leu778=) n.2703T= | |
| 13 | g.32337059G>A | CA387773512 | BRCA2 | c.2704G>A (p.Ala902Thr) c.2335G>A (p.Ala779Thr) n.2704G>A | |
| 13 | g.32337059G>C | CA016149 | BRCA2 | c.2704G>C (p.Ala902Pro) c.2335G>C (p.Ala779Pro) n.2704G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32337059G= | CA2082810695 | BRCA2 | c.2704G= (p.Ala902=) c.2335G= (p.Ala779=) n.2704G= | |
| 13 | g.32337059G>T | CA387773510 | BRCA2 | c.2704G>T (p.Ala902Ser) c.2335G>T (p.Ala779Ser) n.2704G>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337059dup | CA1139663123 | BRCA2 | c.2704dup (p.Ala902GlyfsTer6) c.2335dup (p.Ala779GlyfsTer6) n.2704dup | ClinVar dbSNP |
| 13 | g.32337060C>A | CA387773514 | BRCA2 | c.2705C>A (p.Ala902Asp) c.2336C>A (p.Ala779Asp) n.2705C>A | ClinVar |
| 13 | g.32337060C= | CA2082810702 | BRCA2 | c.2705C= (p.Ala902=) c.2336C= (p.Ala779=) n.2705C= | |
| 13 | g.32337060C>G | CA387773516 | BRCA2 | c.2705C>G (p.Ala902Gly) c.2336C>G (p.Ala779Gly) n.2705C>G | ClinVar |
| 13 | g.32337060C>T | CA247502841 | BRCA2 | c.2705C>T (p.Ala902Val) c.2336C>T (p.Ala779Val) n.2705C>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337060_32337067del | CA2499222114 | BRCA2 | c.2705_2712del (p.Ala902GlufsTer3) c.2336_2343del (p.Ala779GlufsTer3) n.2705_2712del | dbSNP |
| 13 | g.32337061T>A | CA483437204 | BRCA2 | c.2706T>A (p.Ala902=) c.2337T>A (p.Ala779=) n.2706T>A | dbSNP |
| 13 | g.32337061T>C | CA483437205 | BRCA2 | c.2706T>C (p.Ala902=) c.2337T>C (p.Ala779=) n.2706T>C | ClinVar dbSNP |
| 13 | g.32337061T>G | CA483437206 | BRCA2 | c.2706T>G (p.Ala902=) c.2337T>G (p.Ala779=) n.2706T>G | |
| 13 | g.32337062T>A | CA387773518 | BRCA2 | c.2707T>A (p.Leu903Ile) c.2338T>A (p.Leu780Ile) n.2707T>A | dbSNP |
| 13 | g.32337062T>C | CA483437207 | BRCA2 | c.2707T>C (p.Leu903=) c.2338T>C (p.Leu780=) n.2707T>C | |
| 13 | g.32337062T>G | CA387773520 | BRCA2 | c.2707T>G (p.Leu903Val) c.2338T>G (p.Leu780Val) n.2707T>G | |
| 13 | g.32337063T>A | CA387773522 | BRCA2 | c.2708T>A (p.Leu903Ter) c.2339T>A (p.Leu780Ter) n.2708T>A | dbSNP |
| 13 | g.32337063T>C | CA387773523 | BRCA2 | c.2708T>C (p.Leu903Ser) c.2339T>C (p.Leu780Ser) n.2708T>C | dbSNP |
| 13 | g.32337063T>G | CA387773524 | BRCA2 | c.2708T>G (p.Leu903Ter) c.2339T>G (p.Leu780Ter) n.2708T>G | |
| 13 | g.32337064A= | CA2082810713 | BRCA2 | c.2709A= (p.Leu903=) c.2340A= (p.Leu780=) n.2709A= | |
| 13 | g.32337064A>C | CA387773526 | BRCA2 | c.2709A>C (p.Leu903Phe) c.2340A>C (p.Leu780Phe) n.2709A>C | |
| 13 | g.32337064A>G | CA483437209 | BRCA2 | c.2709A>G (p.Leu903=) c.2340A>G (p.Leu780=) n.2709A>G | dbSNP |
| 13 | g.32337064A>T | CA387773528 | BRCA2 | c.2709A>T (p.Leu903Phe) c.2340A>T (p.Leu780Phe) n.2709A>T | dbSNP |
| 13 | g.32337069_32337079del | CA2727924196 | BRCA2 | c.2714_2724del (p.Asn905ThrfsTer3) c.2345_2355del (p.Asn782ThrfsTer3) n.2714_2724del | dbSNP |
| 13 | g.32337065G>A | CA387773532 | BRCA2 | c.2710G>A (p.Gly904Arg) c.2341G>A (p.Gly781Arg) n.2710G>A | ClinVar dbSNP |
| 13 | g.32337065G>C | CA387773529 | BRCA2 | c.2710G>C (p.Gly904Arg) c.2341G>C (p.Gly781Arg) n.2710G>C | dbSNP |
| 13 | g.32337065G>T | CA387773530 | BRCA2 | c.2710G>T (p.Gly904Ter) c.2341G>T (p.Gly781Ter) n.2710G>T | dbSNP |
| 13 | g.32337066dup | CA2082810719 | BRCA2 | c.2711dup (p.Asn905LysfsTer3) c.2342dup (p.Asn782LysfsTer3) n.2711dup | dbSNP |
| 13 | g.32337066G>A | CA387773533 | BRCA2 | c.2711G>A (p.Gly904Glu) c.2342G>A (p.Gly781Glu) n.2711G>A | ClinVar dbSNP |
| 13 | g.32337066G>C | CA387773534 | BRCA2 | c.2711G>C (p.Gly904Ala) c.2342G>C (p.Gly781Ala) n.2711G>C | |
| 13 | g.32337066G= | CA2082810725 | BRCA2 | c.2711G= (p.Gly904=) c.2342G= (p.Gly781=) n.2711G= | |
| 13 | g.32337066G>T | CA387773536 | BRCA2 | c.2711G>T (p.Gly904Val) c.2342G>T (p.Gly781Val) n.2711G>T | dbSNP gnomAD v4 |
| 13 | g.32337066_32337069dup | CA2573053804 | BRCA2 | c.2711_2714dup (p.Asn905LysfsTer4) c.2342_2345dup (p.Asn782LysfsTer4) n.2711_2714dup | ClinVar dbSNP |
| 13 | g.32337067A>C | CA483437210 | BRCA2 | c.2712A>C (p.Gly904=) c.2343A>C (p.Gly781=) n.2712A>C | |
| 13 | g.32337067A>G | CA483437211 | BRCA2 | c.2712A>G (p.Gly904=) c.2343A>G (p.Gly781=) n.2712A>G | |
| 13 | g.32337067A>T | CA483437212 | BRCA2 | c.2712A>T (p.Gly904=) c.2343A>T (p.Gly781=) n.2712A>T | dbSNP |
| 13 | g.32337068A>C | CA387773537 | BRCA2 | c.2713A>C (p.Asn905His) c.2344A>C (p.Asn782His) n.2713A>C | |
| 13 | g.32337068A>G | CA387773539 | BRCA2 | c.2713A>G (p.Asn905Asp) c.2344A>G (p.Asn782Asp) n.2713A>G | |
| 13 | g.32337068A>T | CA387773541 | BRCA2 | c.2713A>T (p.Asn905Tyr) c.2344A>T (p.Asn782Tyr) n.2713A>T | |
| 13 | g.32337069A= | CA2082810729 | BRCA2 | c.2714A= (p.Asn905=) c.2345A= (p.Asn782=) n.2714A= | |
| 13 | g.32337069A>C | CA387773543 | BRCA2 | c.2714A>C (p.Asn905Thr) c.2345A>C (p.Asn782Thr) n.2714A>C | |
| 13 | g.32337069A>G | CA016153 | BRCA2 | c.2714A>G (p.Asn905Ser) c.2345A>G (p.Asn782Ser) n.2714A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32337069A>T | CA387773545 | BRCA2 | c.2714A>T (p.Asn905Ile) c.2345A>T (p.Asn782Ile) n.2714A>T | dbSNP |
| 13 | g.32337070T>A | CA387773547 | BRCA2 | c.2715T>A (p.Asn905Lys) c.2346T>A (p.Asn782Lys) n.2715T>A | dbSNP |
| 13 | g.32337070T>C | CA483437215 | BRCA2 | c.2715T>C (p.Asn905=) c.2346T>C (p.Asn782=) n.2715T>C | dbSNP |
| 13 | g.32337070T>G | CA387773548 | BRCA2 | c.2715T>G (p.Asn905Lys) c.2346T>G (p.Asn782Lys) n.2715T>G | dbSNP |
| 13 | g.32337070T= | CA2082810734 | BRCA2 | c.2715T= (p.Asn905=) c.2346T= (p.Asn782=) n.2715T= | |
| 13 | g.32337070_32337071insTA | CA2695199253 | BRCA2 | c.2715_2716insTA (p.Thr906Ter) c.2346_2347insTA (p.Thr783Ter) n.2715_2716insTA | ClinVar |
| 13 | g.32337071A= | CA2082810744 | BRCA2 | c.2716A= (p.Thr906=) c.2347A= (p.Thr783=) n.2716A= | |
| 13 | g.32337071A>C | CA387773552 | BRCA2 | c.2716A>C (p.Thr906Pro) c.2347A>C (p.Thr783Pro) n.2716A>C | |
| 13 | g.32337071A>G | CA016160 | BRCA2 | c.2716A>G (p.Thr906Ala) c.2347A>G (p.Thr783Ala) n.2716A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32337071A>T | CA387773550 | BRCA2 | c.2716A>T (p.Thr906Ser) c.2347A>T (p.Thr783Ser) n.2716A>T | dbSNP |
| 13 | g.32337071dup | CA10579548 | BRCA2 | c.2716dup (p.Thr906AsnfsTer2) c.2347dup (p.Thr783AsnfsTer2) n.2716dup | ClinVar dbSNP |
| 13 | g.32337072C>A | CA387773556 | BRCA2 | c.2717C>A (p.Thr906Asn) c.2348C>A (p.Thr783Asn) n.2717C>A | dbSNP |
| 13 | g.32337072C= | CA2082810754 | BRCA2 | c.2717C= (p.Thr906=) c.2348C= (p.Thr783=) n.2717C= | |
| 13 | g.32337072C>G | CA387773558 | BRCA2 | c.2717C>G (p.Thr906Ser) c.2348C>G (p.Thr783Ser) n.2717C>G | dbSNP |
| 13 | g.32337072C>T | CA387773560 | BRCA2 | c.2717C>T (p.Thr906Ile) c.2348C>T (p.Thr783Ile) n.2717C>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337073T>A | CA483437220 | BRCA2 | c.2718T>A (p.Thr906=) c.2349T>A (p.Thr783=) n.2718T>A | |
| 13 | g.32337073T>C | CA483437221 | BRCA2 | c.2718T>C (p.Thr906=) c.2349T>C (p.Thr783=) n.2718T>C | ClinVar |
| 13 | g.32337073T>G | CA483437222 | BRCA2 | c.2718T>G (p.Thr906=) c.2349T>G (p.Thr783=) n.2718T>G | |
| 13 | g.32337074_32337082del | CA2622601025 | BRCA2 | c.2719_2727del (p.Lys907_Leu909del) c.2350_2358del (p.Lys784_Leu786del) n.2719_2727del | gnomAD v4 |
| 13 | g.32337074A= | CA2082810769 | BRCA2 | c.2719A= (p.Lys907=) c.2350A= (p.Lys784=) n.2719A= | |
| 13 | g.32337074A>C | CA387773561 | BRCA2 | c.2719A>C (p.Lys907Gln) c.2350A>C (p.Lys784Gln) n.2719A>C | |
| 13 | g.32337074A>G | CA10579549 | BRCA2 | c.2719A>G (p.Lys907Glu) c.2350A>G (p.Lys784Glu) n.2719A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337074A>T | CA387773563 | BRCA2 | c.2719A>T (p.Lys907Ter) c.2350A>T (p.Lys784Ter) n.2719A>T | dbSNP |
| 13 | g.32337075A>C | CA387773566 | BRCA2 | c.2720A>C (p.Lys907Thr) c.2351A>C (p.Lys784Thr) n.2720A>C | dbSNP |
| 13 | g.32337075A>G | CA387773567 | BRCA2 | c.2720A>G (p.Lys907Arg) c.2351A>G (p.Lys784Arg) n.2720A>G | dbSNP |
| 13 | g.32337075A>T | CA387773569 | BRCA2 | c.2720A>T (p.Lys907Met) c.2351A>T (p.Lys784Met) n.2720A>T | dbSNP |
| 13 | g.32337076G>A | CA483437225 | BRCA2 | c.2721G>A (p.Lys907=) c.2352G>A (p.Lys784=) n.2721G>A | ClinVar dbSNP |
| 13 | g.32337076G>C | CA387773571 | BRCA2 | c.2721G>C (p.Lys907Asn) c.2352G>C (p.Lys784Asn) n.2721G>C | ClinVar dbSNP |
| 13 | g.32337076G>T | CA387773573 | BRCA2 | c.2721G>T (p.Lys907Asn) c.2352G>T (p.Lys784Asn) n.2721G>T | dbSNP |
| 13 | g.32337077G>A | CA387773575 | BRCA2 | c.2722G>A (p.Glu908Lys) c.2353G>A (p.Glu785Lys) n.2722G>A | dbSNP |
| 13 | g.32337077G>C | CA387773576 | BRCA2 | c.2722G>C (p.Glu908Gln) c.2353G>C (p.Glu785Gln) n.2722G>C | dbSNP |
| 13 | g.32337077G>T | CA387773578 | BRCA2 | c.2722G>T (p.Glu908Ter) c.2353G>T (p.Glu785Ter) n.2722G>T | ClinVar dbSNP |
| 13 | g.32337078A= | CA2082810796 | BRCA2 | c.2723A= (p.Glu908=) c.2354A= (p.Glu785=) n.2723A= | |
| 13 | g.32337078A>C | CA016168 | BRCA2 | c.2723A>C (p.Glu908Ala) c.2354A>C (p.Glu785Ala) n.2723A>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337078A>G | CA387773581 | BRCA2 | c.2723A>G (p.Glu908Gly) c.2354A>G (p.Glu785Gly) n.2723A>G | dbSNP |
| 13 | g.32337078A>T | CA387773580 | BRCA2 | c.2723A>T (p.Glu908Val) c.2354A>T (p.Glu785Val) n.2723A>T | dbSNP |
| 13 | g.32337079A= | CA2082810805 | BRCA2 | c.2724A= (p.Glu908=) c.2355A= (p.Glu785=) n.2724A= | |
| 13 | g.32337079A>C | CA387773584 | BRCA2 | c.2724A>C (p.Glu908Asp) c.2355A>C (p.Glu785Asp) n.2724A>C | dbSNP COSMIC COSMIC |
| 13 | g.32337079A>G | CA247502858 | BRCA2 | c.2724A>G (p.Glu908=) c.2355A>G (p.Glu785=) n.2724A>G | ClinVar dbSNP |
| 13 | g.32337079A>T | CA387773585 | BRCA2 | c.2724A>T (p.Glu908Asp) c.2355A>T (p.Glu785Asp) n.2724A>T | dbSNP |
| 13 | g.32337079_32337080delinsCA | CA2825002132 | BRCA2 | c.2724_2725delinsCA (p.Glu908_Leu909delinsAspIle) c.2355_2356delinsCA (p.Glu785_Leu786delinsAspIle) n.2724_2725delinsCA | ClinVar |
| 13 | g.32337080C>A | CA10579550 | BRCA2 | c.2725C>A (p.Leu909Ile) c.2356C>A (p.Leu786Ile) n.2725C>A | ClinVar dbSNP |
| 13 | g.32337080C= | CA2082810812 | BRCA2 | c.2725C= (p.Leu909=) c.2356C= (p.Leu786=) n.2725C= | |
| 13 | g.32337080C>G | CA387773586 | BRCA2 | c.2725C>G (p.Leu909Val) c.2356C>G (p.Leu786Val) n.2725C>G | dbSNP |
| 13 | g.32337080C>T | CA387773587 | BRCA2 | c.2725C>T (p.Leu909Phe) c.2356C>T (p.Leu786Phe) n.2725C>T | ClinVar dbSNP |
| 13 | g.32337081T>A | CA387773588 | BRCA2 | c.2726T>A (p.Leu909His) c.2357T>A (p.Leu786His) n.2726T>A | dbSNP |
| 13 | g.32337081T>C | CA387773589 | BRCA2 | c.2726T>C (p.Leu909Pro) c.2357T>C (p.Leu786Pro) n.2726T>C | |
| 13 | g.32337081T>G | CA387773590 | BRCA2 | c.2726T>G (p.Leu909Arg) c.2357T>G (p.Leu786Arg) n.2726T>G | |
| 13 | g.32337082T>A | CA483437233 | BRCA2 | c.2727T>A (p.Leu909=) c.2358T>A (p.Leu786=) n.2727T>A | dbSNP |
| 13 | g.32337082T>C | CA483437234 | BRCA2 | c.2727T>C (p.Leu909=) c.2358T>C (p.Leu786=) n.2727T>C | dbSNP |
| 13 | g.32337082T>G | CA483437237 | BRCA2 | c.2727T>G (p.Leu909=) c.2358T>G (p.Leu786=) n.2727T>G | |
| 13 | g.32337083C>A | CA387773591 | BRCA2 | c.2728C>A (p.His910Asn) c.2359C>A (p.His787Asn) n.2728C>A | dbSNP |
| 13 | g.32337083C= | CA2082810825 | BRCA2 | c.2728C= (p.His910=) c.2359C= (p.His787=) n.2728C= | |
| 13 | g.32337083C>G | CA387773592 | BRCA2 | c.2728C>G (p.His910Asp) c.2359C>G (p.His787Asp) n.2728C>G | dbSNP |
| 13 | g.32337083C>T | CA387773593 | BRCA2 | c.2728C>T (p.His910Tyr) c.2359C>T (p.His787Tyr) n.2728C>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32337084A= | CA2082810834 | BRCA2 | c.2729A= (p.His910=) c.2360A= (p.His787=) n.2729A= | |
| 13 | g.32337084A>C | CA387773594 | BRCA2 | c.2729A>C (p.His910Pro) c.2360A>C (p.His787Pro) n.2729A>C | |
| 13 | g.32337084A>G | CA6940625 | BRCA2 | c.2729A>G (p.His910Arg) c.2360A>G (p.His787Arg) n.2729A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337084A>T | CA387773595 | BRCA2 | c.2729A>T (p.His910Leu) c.2360A>T (p.His787Leu) n.2729A>T | dbSNP |
| 13 | g.32337085T>A | CA387773597 | BRCA2 | c.2730T>A (p.His910Gln) c.2361T>A (p.His787Gln) n.2730T>A | dbSNP |
| 13 | g.32337085T>C | CA483437242 | BRCA2 | c.2730T>C (p.His910=) c.2361T>C (p.His787=) n.2730T>C | ClinVar |
| 13 | g.32337085T>G | CA387773596 | BRCA2 | c.2730T>G (p.His910Gln) c.2361T>G (p.His787Gln) n.2730T>G | dbSNP |
| 13 | g.32337085_32337086delinsTG | CA2082810837 | BRCA2 | c.2730_2731delinsTG (p.His910=) c.2361_2362delinsTG (p.His787=) n.2730_2731delinsTG | |
| 13 | g.32337086del | CA016174 | BRCA2 | c.2731del (p.Glu911LysfsTer4) c.2362del (p.Glu788LysfsTer4) n.2731del | ClinVar dbSNP |
| 13 | g.32337086G>A | CA387773598 | BRCA2 | c.2731G>A (p.Glu911Lys) c.2362G>A (p.Glu788Lys) n.2731G>A | dbSNP |
| 13 | g.32337086G>C | CA387773599 | BRCA2 | c.2731G>C (p.Glu911Gln) c.2362G>C (p.Glu788Gln) n.2731G>C | ClinVar dbSNP |
| 13 | g.32337086G= | CA2082810850 | BRCA2 | c.2731G= (p.Glu911=) c.2362G= (p.Glu788=) n.2731G= | |
| 13 | g.32337086G>T | CA387773600 | BRCA2 | c.2731G>T (p.Glu911Ter) c.2362G>T (p.Glu788Ter) n.2731G>T | dbSNP |
| 13 | g.32337087A>C | CA387773601 | BRCA2 | c.2732A>C (p.Glu911Ala) c.2363A>C (p.Glu788Ala) n.2732A>C | |
| 13 | g.32337087A>G | CA387773602 | BRCA2 | c.2732A>G (p.Glu911Gly) c.2363A>G (p.Glu788Gly) n.2732A>G | ClinVar |
| 13 | g.32337087A>T | CA387773603 | BRCA2 | c.2732A>T (p.Glu911Val) c.2363A>T (p.Glu788Val) n.2732A>T | dbSNP |
| 13 | g.32337089dup | CA2580087297 | BRCA2 | c.2734dup (p.Thr912AsnfsTer24) c.2365dup (p.Thr789AsnfsTer24) n.2734dup | ClinVar |
| 13 | g.32337088A>C | CA387773605 | BRCA2 | c.2733A>C (p.Glu911Asp) c.2364A>C (p.Glu788Asp) n.2733A>C | |
| 13 | g.32337088A>G | CA483437247 | BRCA2 | c.2733A>G (p.Glu911=) c.2364A>G (p.Glu788=) n.2733A>G | dbSNP |
| 13 | g.32337088A>T | CA387773604 | BRCA2 | c.2733A>T (p.Glu911Asp) c.2364A>T (p.Glu788Asp) n.2733A>T | dbSNP |
| 13 | g.32337089A= | CA2082810859 | BRCA2 | c.2734A= (p.Thr912=) c.2365A= (p.Thr789=) n.2734A= | |
| 13 | g.32337089A>C | CA387773606 | BRCA2 | c.2734A>C (p.Thr912Pro) c.2365A>C (p.Thr789Pro) n.2734A>C | |
| 13 | g.32337089A>G | CA387773607 | BRCA2 | c.2734A>G (p.Thr912Ala) c.2365A>G (p.Thr789Ala) n.2734A>G | ClinVar dbSNP |
| 13 | g.32337089A>T | CA387773608 | BRCA2 | c.2734A>T (p.Thr912Ser) c.2365A>T (p.Thr789Ser) n.2734A>T | |
| 13 | g.32337090C>A | CA387773609 | BRCA2 | c.2735C>A (p.Thr912Lys) c.2366C>A (p.Thr789Lys) n.2735C>A | dbSNP |
| 13 | g.32337090C= | CA2082810870 | BRCA2 | c.2735C= (p.Thr912=) c.2366C= (p.Thr789=) n.2735C= | |
| 13 | g.32337090C>G | CA6940626 | BRCA2 | c.2735C>G (p.Thr912Arg) c.2366C>G (p.Thr789Arg) n.2735C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32337090C>T | CA016183 | BRCA2 | c.2735C>T (p.Thr912Ile) c.2366C>T (p.Thr789Ile) n.2735C>T | ClinVar dbSNP |
| 13 | g.32337091A>C | CA483437324 | BRCA2 | c.2736A>C (p.Thr912=) c.2367A>C (p.Thr789=) n.2736A>C | |
| 13 | g.32337091A>G | CA483437325 | BRCA2 | c.2736A>G (p.Thr912=) c.2367A>G (p.Thr789=) n.2736A>G | ClinVar |
| 13 | g.32337091A>T | CA483437323 | BRCA2 | c.2736A>T (p.Thr912=) c.2367A>T (p.Thr789=) n.2736A>T | |
| 13 | g.32337091_32337096delinsAGACTT | CA2082810879 | BRCA2 | c.2736_2741delinsAGACTT (p.Thr912=) c.2367_2372delinsAGACTT (p.Thr789=) n.2736_2741delinsAGACTT | |
| 13 | g.32337092G>A | CA387773612 | BRCA2 | c.2737G>A (p.Asp913Asn) c.2368G>A (p.Asp790Asn) n.2737G>A | dbSNP |
| 13 | g.32337092G>C | CA387773610 | BRCA2 | c.2737G>C (p.Asp913His) c.2368G>C (p.Asp790His) n.2737G>C | dbSNP |
| 13 | g.32337092G>T | CA387773611 | BRCA2 | c.2737G>T (p.Asp913Tyr) c.2368G>T (p.Asp790Tyr) n.2737G>T | gnomAD v4 |
| 13 | g.32337098_32337102del | CA016222 | BRCA2 | c.2743_2747del (p.Thr915CysfsTer19) c.2374_2378del (p.Thr792CysfsTer19) n.2743_2747del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337093A>C | CA387773613 | BRCA2 | c.2738A>C (p.Asp913Ala) c.2369A>C (p.Asp790Ala) n.2738A>C | |
| 13 | g.32337093A>G | CA387773614 | BRCA2 | c.2738A>G (p.Asp913Gly) c.2369A>G (p.Asp790Gly) n.2738A>G | ClinVar |
| 13 | g.32337093A>T | CA387773615 | BRCA2 | c.2738A>T (p.Asp913Val) c.2369A>T (p.Asp790Val) n.2738A>T | |
| 13 | g.32337094C>A | CA387773616 | BRCA2 | c.2739C>A (p.Asp913Glu) c.2370C>A (p.Asp790Glu) n.2739C>A | dbSNP |
| 13 | g.32337094C= | CA2082810896 | BRCA2 | c.2739C= (p.Asp913=) c.2370C= (p.Asp790=) n.2739C= | |
| 13 | g.32337094C>G | CA387773617 | BRCA2 | c.2739C>G (p.Asp913Glu) c.2370C>G (p.Asp790Glu) n.2739C>G | dbSNP |
| 13 | g.32337094C>T | CA016192 | BRCA2 | c.2739C>T (p.Asp913=) c.2370C>T (p.Asp790=) n.2739C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337095T>A | CA387773618 | BRCA2 | c.2740T>A (p.Leu914Met) c.2371T>A (p.Leu791Met) n.2740T>A | dbSNP |
| 13 | g.32337095T>C | CA483437326 | BRCA2 | c.2740T>C (p.Leu914=) c.2371T>C (p.Leu791=) n.2740T>C | ClinVar |
| 13 | g.32337095T>G | CA387773619 | BRCA2 | c.2740T>G (p.Leu914Val) c.2371T>G (p.Leu791Val) n.2740T>G | |
| 13 | g.32337096T>A | CA387773620 | BRCA2 | c.2741T>A (p.Leu914Ter) c.2372T>A (p.Leu791Ter) n.2741T>A | dbSNP |
| 13 | g.32337096T>C | CA387773621 | BRCA2 | c.2741T>C (p.Leu914Ser) c.2372T>C (p.Leu791Ser) n.2741T>C | |
| 13 | g.32337096T>G | CA387773622 | BRCA2 | c.2741T>G (p.Leu914Trp) c.2372T>G (p.Leu791Trp) n.2741T>G | |
| 13 | g.32337097G>A | CA483437327 | BRCA2 | c.2742G>A (p.Leu914=) c.2373G>A (p.Leu791=) n.2742G>A | ClinVar dbSNP |
| 13 | g.32337097G>C | CA6940627 | BRCA2 | c.2742G>C (p.Leu914Phe) c.2373G>C (p.Leu791Phe) n.2742G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32337097G= | CA2082810903 | BRCA2 | c.2742G= (p.Leu914=) c.2373G= (p.Leu791=) n.2742G= | |
| 13 | g.32337097G>T | CA387773623 | BRCA2 | c.2742G>T (p.Leu914Phe) c.2373G>T (p.Leu791Phe) n.2742G>T | ClinVar dbSNP |
| 13 | g.32337098A>C | CA387773624 | BRCA2 | c.2743A>C (p.Thr915Pro) c.2374A>C (p.Thr792Pro) n.2743A>C | dbSNP |
| 13 | g.32337098A>G | CA387773625 | BRCA2 | c.2743A>G (p.Thr915Ala) c.2374A>G (p.Thr792Ala) n.2743A>G | dbSNP |
| 13 | g.32337098A>T | CA387773626 | BRCA2 | c.2743A>T (p.Thr915Ser) c.2374A>T (p.Thr792Ser) n.2743A>T | ClinVar |
| 13 | g.32337099C>A | CA387773627 | BRCA2 | c.2744C>A (p.Thr915Asn) c.2375C>A (p.Thr792Asn) n.2744C>A | ClinVar |
| 13 | g.32337099C= | CA2082810913 | BRCA2 | c.2744C= (p.Thr915=) c.2375C= (p.Thr792=) n.2744C= | |
| 13 | g.32337099C>G | CA016236 | BRCA2 | c.2744C>G (p.Thr915Ser) c.2375C>G (p.Thr792Ser) n.2744C>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337099C>T | CA387773628 | BRCA2 | c.2744C>T (p.Thr915Ile) c.2375C>T (p.Thr792Ile) n.2744C>T | ClinVar dbSNP |
| 13 | g.32337099_32337101delinsCTT | CA2082810915 | BRCA2 | c.2744_2746delinsCTT (p.Thr915=) c.2375_2377delinsCTT (p.Thr792=) n.2744_2746delinsCTT | |
| 13 | g.32337100T>A | CA483437330 | BRCA2 | c.2745T>A (p.Thr915=) c.2376T>A (p.Thr792=) n.2745T>A | dbSNP |
| 13 | g.32337100T>C | CA483437329 | BRCA2 | c.2745T>C (p.Thr915=) c.2376T>C (p.Thr792=) n.2745T>C | |
| 13 | g.32337100T>G | CA483437328 | BRCA2 | c.2745T>G (p.Thr915=) c.2376T>G (p.Thr792=) n.2745T>G | |
| 13 | g.32337100_32337101del | CA10589168 | BRCA2 | c.2745_2746del (p.Val917LysfsTer18) c.2376_2377del (p.Val794LysfsTer18) n.2745_2746del | ClinVar dbSNP |
| 13 | g.32337101_32337105dup | CA2573149398 | BRCA2 | c.2746_2750dup (p.Asn918ValfsTer2) c.2377_2381dup (p.Asn795ValfsTer2) n.2746_2750dup | ClinVar dbSNP |
| 13 | g.32337101T>A | CA387773631 | BRCA2 | c.2746T>A (p.Cys916Ser) c.2377T>A (p.Cys793Ser) n.2746T>A | dbSNP |
| 13 | g.32337101T>C | CA387773630 | BRCA2 | c.2746T>C (p.Cys916Arg) c.2377T>C (p.Cys793Arg) n.2746T>C | |
| 13 | g.32337101T>G | CA387773629 | BRCA2 | c.2746T>G (p.Cys916Gly) c.2377T>G (p.Cys793Gly) n.2746T>G |