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New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32359467_32364093del | CA2580087377 | BRCA2 | c.7805+1538_8331+560del c.7436+1538_7962+560del c.272+1538_798+560del c.7805+1538_8339+560del c.370+1538_896+560del c.7709+1538_8235+560del | ClinVar |
| 13 | g.32362656_32362674del | CA2580087419 | BRCA2 | c.7939_7957del (p.Leu2647PhefsTer4) c.7570_7588del (p.Leu2524PhefsTer4) c.406_424del (p.Leu136PhefsTer4) c.7947_7965del (n.[c.7947_7965del;Ter2650SerextTer8]) c.504_522del c.7843_7861del (p.Leu2615PhefsTer4) | ClinVar |
| 13 | g.32362672T>A | CA387747264 | BRCA2 | c.7955T>A (p.Val2652Glu) c.7586T>A (p.Val2529Glu) c.422T>A (p.Val141Glu) c.7963T>A (n.7963T>A) c.520T>A c.7859T>A (p.Val2620Glu) | ClinVar dbSNP |
| 13 | g.32362672T>C | CA387747266 | BRCA2 | c.7955T>C (p.Val2652Ala) c.7586T>C (p.Val2529Ala) c.422T>C (p.Val141Ala) c.7963T>C (n.7963T>C) c.520T>C c.7859T>C (p.Val2620Ala) | |
| 13 | g.32362672T>G | CA387747262 | BRCA2 | c.7955T>G (p.Val2652Gly) c.7586T>G (p.Val2529Gly) c.422T>G (p.Val141Gly) c.7963T>G (n.7963T>G) c.520T>G c.7859T>G (p.Val2620Gly) | ClinVar dbSNP gnomAD v4 |
| 13 | g.32362672T= | CA2082832112 | BRCA2 | c.7955T= (p.Val2652=) c.7586T= (p.Val2529=) c.422T= (p.Val141=) c.7963T= (n.7963T=) c.520T= c.7859T= (p.Val2620=) | |
| 13 | g.32362673_32362676dup | CA2499222315 | BRCA2 | c.7956_7959dup (p.Leu2654AlafsTer9) c.7587_7590dup (p.Leu2531AlafsTer9) c.423_426dup (p.Leu143AlafsTer9) c.7964_7967dup (n.7964_7967dup) c.521_524dup c.7860_7863dup (p.Leu2622AlafsTer9) | ClinVar dbSNP |
| 13 | g.32362673G>A | CA483261027 | BRCA2 | c.7956G>A (p.Val2652=) c.7587G>A (p.Val2529=) c.423G>A (p.Val141=) c.7964G>A (n.7964G>A) c.521G>A c.7860G>A (p.Val2620=) | ClinVar dbSNP |
| 13 | g.32362673G>C | CA483261028 | BRCA2 | c.7956G>C (p.Val2652=) c.7587G>C (p.Val2529=) c.423G>C (p.Val141=) c.7964G>C (n.7964G>C) c.521G>C c.7860G>C (p.Val2620=) | dbSNP |
| 13 | g.32362673G>T | CA483261029 | BRCA2 | c.7956G>T (p.Val2652=) c.7587G>T (p.Val2529=) c.423G>T (p.Val141=) c.7964G>T (n.7964G>T) c.521G>T c.7860G>T (p.Val2620=) | |
| 13 | g.32362673_32362674del | CA2825002146 | BRCA2 | c.7956_7957del (p.Leu2653SerfsTer8) c.7587_7588del (p.Leu2530SerfsTer8) c.423_424del (p.Leu142SerfsTer8) c.7964_7965del (n.7964_7965del) c.521_522del c.7860_7861del (p.Leu2621SerfsTer8) | ClinVar |
| 13 | g.32362673_32362676delinsGCTT | CA2082832117 | BRCA2 | c.7956_7959delinsGCTT (p.Val2652=) c.7587_7590delinsGCTT (p.Val2529=) c.423_426delinsGCTT (p.Val141=) c.7964_7967delinsGCTT (n.7964_7967delinsGCTT) c.521_524delinsGCTT c.7860_7863delinsGCTT (p.Val2620=) | |
| 13 | g.32362674C>A | CA387747269 | BRCA2 | c.7957C>A (p.Leu2653Ile) c.7588C>A (p.Leu2530Ile) c.424C>A (p.Leu142Ile) c.7965C>A (n.7965C>A) c.522C>A c.7861C>A (p.Leu2621Ile) | dbSNP |
| 13 | g.32362674C= | CA2082832124 | BRCA2 | c.7957C= (p.Leu2653=) c.7588C= (p.Leu2530=) c.424C= (p.Leu142=) c.7965C= (n.7965C=) c.522C= c.7861C= (p.Leu2621=) | |
| 13 | g.32362674C>G | CA387747272 | BRCA2 | c.7957C>G (p.Leu2653Val) c.7588C>G (p.Leu2530Val) c.424C>G (p.Leu142Val) c.7965C>G (n.7965C>G) c.522C>G c.7861C>G (p.Leu2621Val) | ClinVar dbSNP |
| 13 | g.32362674C>T | CA6941163 | BRCA2 | c.7957C>T (p.Leu2653Phe) c.7588C>T (p.Leu2530Phe) c.424C>T (p.Leu142Phe) c.7965C>T (n.7965C>T) c.522C>T c.7861C>T (p.Leu2621Phe) | dbSNP ExAC gnomAD v2 |
| 13 | g.32362674_32362675delinsCT | CA2082832119 | BRCA2 | c.7957_7958delinsCT (p.Leu2653=) c.7588_7589delinsCT (p.Leu2530=) c.424_425delinsCT (p.Leu142=) c.7965_7966delinsCT (n.7965_7966delinsCT) c.522_523delinsCT c.7861_7862delinsCT (p.Leu2621=) | |
| 13 | g.32362678_32362680del | CA915946883 | BRCA2 | c.7961_7963del (p.Leu2654del) c.7592_7594del (p.Leu2531del) c.428_430del (p.Leu143del) c.7969_7971del (n.7969_7971del) c.526_528del c.7865_7867del (p.Leu2622del) | ClinVar dbSNP |
| 13 | g.32362675T>A | CA387747275 | BRCA2 | c.7958T>A (p.Leu2653His) c.7589T>A (p.Leu2530His) c.425T>A (p.Leu142His) c.7966T>A (n.7966T>A) c.523T>A c.7862T>A (p.Leu2621His) | dbSNP |
| 13 | g.32362675T>C | CA025354 | BRCA2 | c.7958T>C (p.Leu2653Pro) c.7589T>C (p.Leu2530Pro) c.425T>C (p.Leu142Pro) c.7966T>C (n.7966T>C) c.523T>C c.7862T>C (p.Leu2621Pro) | ClinVar dbSNP gnomAD v4 |
| 13 | g.32362675T>G | CA16614368 | BRCA2 | c.7958T>G (p.Leu2653Arg) c.7589T>G (p.Leu2530Arg) c.425T>G (p.Leu142Arg) c.7966T>G (n.7966T>G) c.523T>G c.7862T>G (p.Leu2621Arg) | ClinVar dbSNP |
| 13 | g.32362675T= | CA2082832137 | BRCA2 | c.7958T= (p.Leu2653=) c.7589T= (p.Leu2530=) c.425T= (p.Leu142=) c.7966T= (n.7966T=) c.523T= c.7862T= (p.Leu2621=) | |
| 13 | g.32362675_32362676dup | CA891843893 | BRCA2 | c.7958_7959dup (p.Leu2654PhefsTer4) c.7589_7590dup (p.Leu2531PhefsTer4) c.425_426dup (p.Leu143PhefsTer4) c.7966_7967dup (n.7966_7967dup) c.523_524dup c.7862_7863dup (p.Leu2622PhefsTer4) | ClinVar dbSNP |
| 13 | g.32362676del | CA1139663136 | BRCA2 | c.7959del (p.Leu2654PhefsTer3) c.7590del (p.Leu2531PhefsTer3) c.426del (p.Leu143PhefsTer3) c.7967del (n.7967del) c.524del c.7863del (p.Leu2622PhefsTer3) | ClinVar dbSNP |
| 13 | g.32362676T>A | CA483261031 | BRCA2 | c.7959T>A (p.Leu2653=) c.7590T>A (p.Leu2530=) c.426T>A (p.Leu142=) c.7967T>A (n.7967T>A) c.524T>A c.7863T>A (p.Leu2621=) | dbSNP |
| 13 | g.32362676T>C | CA483261034 | BRCA2 | c.7959T>C (p.Leu2653=) c.7590T>C (p.Leu2530=) c.426T>C (p.Leu142=) c.7967T>C (n.7967T>C) c.524T>C c.7863T>C (p.Leu2621=) | ClinVar |
| 13 | g.32362676T>G | CA483261032 | BRCA2 | c.7959T>G (p.Leu2653=) c.7590T>G (p.Leu2530=) c.426T>G (p.Leu142=) c.7967T>G (n.7967T>G) c.524T>G c.7863T>G (p.Leu2621=) | ClinVar dbSNP |
| 13 | g.32362676T= | CA2082832157 | BRCA2 | c.7959T= (p.Leu2653=) c.7590T= (p.Leu2530=) c.426T= (p.Leu142=) c.7967T= (n.7967T=) c.524T= c.7863T= (p.Leu2621=) | |
| 13 | g.32362677C>A | CA387747280 | BRCA2 | c.7960C>A (p.Leu2654Ile) c.7591C>A (p.Leu2531Ile) c.427C>A (p.Leu143Ile) c.7968C>A (n.7968C>A) c.525C>A c.7864C>A (p.Leu2622Ile) | |
| 13 | g.32362677C>G | CA387747282 | BRCA2 | c.7960C>G (p.Leu2654Val) c.7591C>G (p.Leu2531Val) c.427C>G (p.Leu143Val) c.7968C>G (n.7968C>G) c.525C>G c.7864C>G (p.Leu2622Val) | dbSNP |
| 13 | g.32362677C>T | CA387747284 | BRCA2 | c.7960C>T (p.Leu2654Phe) c.7591C>T (p.Leu2531Phe) c.427C>T (p.Leu143Phe) c.7968C>T (n.7968C>T) c.525C>T c.7864C>T (p.Leu2622Phe) | dbSNP COSMIC COSMIC |
| 13 | g.32362678T>A | CA387747286 | BRCA2 | c.7961T>A (p.Leu2654His) c.7592T>A (p.Leu2531His) c.428T>A (p.Leu143His) c.7969T>A (n.7969T>A) c.526T>A c.7865T>A (p.Leu2622His) | |
| 13 | g.32362678T>C | CA025355 | BRCA2 | c.7961T>C (p.Leu2654Pro) c.7592T>C (p.Leu2531Pro) c.428T>C (p.Leu143Pro) c.7969T>C (n.7969T>C) c.526T>C c.7865T>C (p.Leu2622Pro) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32362678T>G | CA387747289 | BRCA2 | c.7961T>G (p.Leu2654Arg) c.7592T>G (p.Leu2531Arg) c.428T>G (p.Leu143Arg) c.7969T>G (n.7969T>G) c.526T>G c.7865T>G (p.Leu2622Arg) | |
| 13 | g.32362678T= | CA2082832164 | BRCA2 | c.7961T= (p.Leu2654=) c.7592T= (p.Leu2531=) c.428T= (p.Leu143=) c.7969T= (n.7969T=) c.526T= c.7865T= (p.Leu2622=) | |
| 13 | g.32362679T>A | CA483261039 | BRCA2 | c.7962T>A (p.Leu2654=) c.7593T>A (p.Leu2531=) c.429T>A (p.Leu143=) c.7970T>A (n.7970T>A) c.527T>A c.7866T>A (p.Leu2622=) | dbSNP |
| 13 | g.32362679T>C | CA483261041 | BRCA2 | c.7962T>C (p.Leu2654=) c.7593T>C (p.Leu2531=) c.429T>C (p.Leu143=) c.7970T>C (n.7970T>C) c.527T>C c.7866T>C (p.Leu2622=) | |
| 13 | g.32362679T>G | CA483261043 | BRCA2 | c.7962T>G (p.Leu2654=) c.7593T>G (p.Leu2531=) c.429T>G (p.Leu143=) c.7970T>G (n.7970T>G) c.527T>G c.7866T>G (p.Leu2622=) | |
| 13 | g.32362679_32362680delinsTC | CA2082832166 | BRCA2 | c.7962_7963delinsTC (p.Leu2654=) c.7593_7594delinsTC (p.Leu2531=) c.429_430delinsTC (p.Leu143=) c.7970_7971delinsTC (n.7970_7971delinsTC) c.527_528delinsTC c.7866_7867delinsTC (p.Leu2622=) | |
| 13 | g.32362680del | CA025357 | BRCA2 | c.7963del (p.Gln2655AsnfsTer2) c.7594del (p.Gln2532AsnfsTer2) c.430del (p.Gln144AsnfsTer2) c.7971del (n.7971del) c.528del c.7867del (p.Gln2623AsnfsTer2) | ClinVar dbSNP |
| 13 | g.32362680C>A | CA387747299 | BRCA2 | c.7963C>A (p.Gln2655Lys) c.7594C>A (p.Gln2532Lys) c.430C>A (p.Gln144Lys) c.7971C>A (n.7971C>A) c.528C>A c.7867C>A (p.Gln2623Lys) | |
| 13 | g.32362680C= | CA2082832173 | BRCA2 | c.7963C= (p.Gln2655=) c.7594C= (p.Gln2532=) c.430C= (p.Gln144=) c.7971C= (n.7971C=) c.528C= c.7867C= (p.Gln2623=) | |
| 13 | g.32362680C>G | CA387747297 | BRCA2 | c.7963C>G (p.Gln2655Glu) c.7594C>G (p.Gln2532Glu) c.430C>G (p.Gln144Glu) c.7971C>G (n.7971C>G) c.528C>G c.7867C>G (p.Gln2623Glu) | |
| 13 | g.32362680C>T | CA025356 | BRCA2 | c.7963C>T (p.Gln2655Ter) c.7594C>T (p.Gln2532Ter) c.430C>T (p.Gln144Ter) c.7971C>T (n.7971C>T) c.528C>T c.7867C>T (p.Gln2623Ter) | ClinVar dbSNP COSMIC COSMIC |
| 13 | g.32362680_32362681delinsCA | CA2082832178 | BRCA2 | c.7963_7964delinsCA (p.Gln2655=) c.7594_7595delinsCA (p.Gln2532=) c.430_431delinsCA (p.Gln144=) c.7971_7972delinsCA (n.7971_7972delinsCA) c.528_529delinsCA c.7867_7868delinsCA (p.Gln2623=) | |
| 13 | g.32362680_32362691del | CA1139771309 | BRCA2 | c.7963_7974del (p.Gln2655_Tyr2658del) c.7594_7605del (p.Gln2532_Tyr2535del) c.430_441del (p.Gln144_Tyr147del) c.7971_7982del (n.7971_7982del) c.528_539del c.7867_7878del (p.Gln2623_Tyr2626del) | |
| 13 | g.32362681A= | CA2082832187 | BRCA2 | c.7964A= (p.Gln2655=) c.7595A= (p.Gln2532=) c.431A= (p.Gln144=) c.7972A= (n.7972A=) c.529A= c.7868A= (p.Gln2623=) | |
| 13 | g.32362681A>C | CA387747301 | BRCA2 | c.7964A>C (p.Gln2655Pro) c.7595A>C (p.Gln2532Pro) c.431A>C (p.Gln144Pro) c.7972A>C (n.7972A>C) c.529A>C c.7868A>C (p.Gln2623Pro) | |
| 13 | g.32362681A>G | CA025358 | BRCA2 | c.7964A>G (p.Gln2655Arg) c.7595A>G (p.Gln2532Arg) c.431A>G (p.Gln144Arg) c.7972A>G (n.7972A>G) c.529A>G c.7868A>G (p.Gln2623Arg) | ClinVar dbSNP gnomAD v4 |
| 13 | g.32362681A>T | CA387747306 | BRCA2 | c.7964A>T (p.Gln2655Leu) c.7595A>T (p.Gln2532Leu) c.431A>T (p.Gln144Leu) c.7972A>T (n.7972A>T) c.529A>T c.7868A>T (p.Gln2623Leu) | ClinVar dbSNP |
| 13 | g.32362681_32362682del | CA2582341813 | BRCA2 | c.7964_7965del (p.Gln2655ProfsTer6) c.7595_7596del (p.Gln2532ProfsTer6) c.431_432del (p.Gln144ProfsTer6) c.7972_7973del (n.7972_7973del) c.529_530del c.7868_7869del (p.Gln2623ProfsTer6) | ClinVar |
| 13 | g.32362682del | CA913190910 | BRCA2 | c.7965del (p.Gln2655HisfsTer2) c.7596del (p.Gln2532HisfsTer2) c.432del (p.Gln144HisfsTer2) c.7973del (n.7973del) c.530del c.7869del (p.Gln2623HisfsTer2) | ClinVar dbSNP |
| 13 | g.32362682A= | CA2082832192 | BRCA2 | c.7965A= (p.Gln2655=) c.7596A= (p.Gln2532=) c.432A= (p.Gln144=) c.7973A= (n.7973A=) c.530A= c.7869A= (p.Gln2623=) | |
| 13 | g.32362682A>C | CA387747309 | BRCA2 | c.7965A>C (p.Gln2655His) c.7596A>C (p.Gln2532His) c.432A>C (p.Gln144His) c.7973A>C (n.7973A>C) c.530A>C c.7869A>C (p.Gln2623His) | |
| 13 | g.32362682A>G | CA247475304 | BRCA2 | c.7965A>G (p.Gln2655=) c.7596A>G (p.Gln2532=) c.432A>G (p.Gln144=) c.7973A>G (n.7973A>G) c.530A>G c.7869A>G (p.Gln2623=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32362682A>T | CA387747311 | BRCA2 | c.7965A>T (p.Gln2655His) c.7596A>T (p.Gln2532His) c.432A>T (p.Gln144His) c.7973A>T (n.7973A>T) c.530A>T c.7869A>T (p.Gln2623His) | ClinVar dbSNP |
| 13 | g.32362683C>A | CA387747314 | BRCA2 | c.7966C>A (p.Leu2656Ile) c.7597C>A (p.Leu2533Ile) c.433C>A (p.Leu145Ile) c.7974C>A (n.7974C>A) c.531C>A c.7870C>A (p.Leu2624Ile) | dbSNP COSMIC COSMIC |
| 13 | g.32362683C= | CA2082832202 | BRCA2 | c.7966C= (p.Leu2656=) c.7597C= (p.Leu2533=) c.433C= (p.Leu145=) c.7974C= (n.7974C=) c.531C= c.7870C= (p.Leu2624=) | |
| 13 | g.32362683C>G | CA387747316 | BRCA2 | c.7966C>G (p.Leu2656Val) c.7597C>G (p.Leu2533Val) c.433C>G (p.Leu145Val) c.7974C>G (n.7974C>G) c.531C>G c.7870C>G (p.Leu2624Val) | ClinVar dbSNP |
| 13 | g.32362683C>T | CA483261053 | BRCA2 | c.7966C>T (p.Leu2656=) c.7597C>T (p.Leu2533=) c.433C>T (p.Leu145=) c.7974C>T (n.7974C>T) c.531C>T c.7870C>T (p.Leu2624=) | ClinVar dbSNP gnomAD v4 |
| 13 | g.32362684T>A | CA16613950 | BRCA2 | c.7967T>A (p.Leu2656Gln) c.7598T>A (p.Leu2533Gln) c.434T>A (p.Leu145Gln) c.7975T>A (n.7975T>A) c.532T>A c.7871T>A (p.Leu2624Gln) | ClinVar dbSNP |
| 13 | g.32362684T>C | CA10575929 | BRCA2 | c.7967T>C (p.Leu2656Pro) c.7598T>C (p.Leu2533Pro) c.434T>C (p.Leu145Pro) c.7975T>C (n.7975T>C) c.532T>C c.7871T>C (p.Leu2624Pro) | ClinVar dbSNP |
| 13 | g.32362684T>G | CA387747320 | BRCA2 | c.7967T>G (p.Leu2656Arg) c.7598T>G (p.Leu2533Arg) c.434T>G (p.Leu145Arg) c.7975T>G (n.7975T>G) c.532T>G c.7871T>G (p.Leu2624Arg) | |
| 13 | g.32362684T= | CA2082832208 | BRCA2 | c.7967T= (p.Leu2656=) c.7598T= (p.Leu2533=) c.434T= (p.Leu145=) c.7975T= (n.7975T=) c.532T= c.7871T= (p.Leu2624=) | |
| 13 | g.32362688_32362704del | CA2580612214 | BRCA2 | c.7971_7976+11del c.7602_7607+11del c.438_443+11del c.7979_7984+11del c.536_541+11del c.7875_7880+11del | |
| 13 | g.32362685A= | CA2082832235 | BRCA2 | c.7968A= (p.Leu2656=) c.7599A= (p.Leu2533=) c.435A= (p.Leu145=) c.7976A= (n.7976A=) c.533A= c.7872A= (p.Leu2624=) | |
| 13 | g.32362685A>C | CA483261054 | BRCA2 | c.7968A>C (p.Leu2656=) c.7599A>C (p.Leu2533=) c.435A>C (p.Leu145=) c.7976A>C (n.7976A>C) c.533A>C c.7872A>C (p.Leu2624=) | |
| 13 | g.32362685A>G | CA483261055 | BRCA2 | c.7968A>G (p.Leu2656=) c.7599A>G (p.Leu2533=) c.435A>G (p.Leu145=) c.7976A>G (n.7976A>G) c.533A>G c.7872A>G (p.Leu2624=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32362685A>T | CA483261056 | BRCA2 | c.7968A>T (p.Leu2656=) c.7599A>T (p.Leu2533=) c.435A>T (p.Leu145=) c.7976A>T (n.7976A>T) c.533A>T c.7872A>T (p.Leu2624=) | |
| 13 | g.32362688dup | CA2727917416 | BRCA2 | c.7971dup (p.Tyr2658IlefsTer4) c.7602dup (p.Tyr2535IlefsTer4) c.438dup (p.Tyr147IlefsTer4) c.7979dup (n.7979dup) c.536dup c.7875dup (p.Tyr2626IlefsTer4) | dbSNP |
| 13 | g.32362686A>C | CA387747323 | BRCA2 | c.7969A>C (p.Lys2657Gln) c.7600A>C (p.Lys2534Gln) c.436A>C (p.Lys146Gln) c.7977A>C (n.7977A>C) c.534A>C c.7873A>C (p.Lys2625Gln) | |
| 13 | g.32362686A>G | CA387747324 | BRCA2 | c.7969A>G (p.Lys2657Glu) c.7600A>G (p.Lys2534Glu) c.436A>G (p.Lys146Glu) c.7977A>G (n.7977A>G) c.534A>G c.7873A>G (p.Lys2625Glu) | ClinVar dbSNP |
| 13 | g.32362686A>T | CA387747327 | BRCA2 | c.7969A>T (p.Lys2657Ter) c.7600A>T (p.Lys2534Ter) c.436A>T (p.Lys146Ter) c.7977A>T (n.7977A>T) c.534A>T c.7873A>T (p.Lys2625Ter) | ClinVar gnomAD v4 |
| 13 | g.32362688_32362697del | CA2580087432 | BRCA2 | c.7971_7976+4del c.7602_7607+4del c.438_443+4del c.7979_7984+4del c.536_541+4del c.7875_7880+4del | ClinVar |
| 13 | g.32362687A= | CA2082832254 | BRCA2 | c.7970A= (p.Lys2657=) c.7601A= (p.Lys2534=) c.437A= (p.Lys146=) c.7978A= (n.7978A=) c.535A= c.7874A= (p.Lys2625=) | |
| 13 | g.32362687A>C | CA387747333 | BRCA2 | c.7970A>C (p.Lys2657Thr) c.7601A>C (p.Lys2534Thr) c.437A>C (p.Lys146Thr) c.7978A>C (n.7978A>C) c.535A>C c.7874A>C (p.Lys2625Thr) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32362687A>G | CA387747335 | BRCA2 | c.7970A>G (p.Lys2657Arg) c.7601A>G (p.Lys2534Arg) c.437A>G (p.Lys146Arg) c.7978A>G (n.7978A>G) c.535A>G c.7874A>G (p.Lys2625Arg) | |
| 13 | g.32362687A>T | CA387747331 | BRCA2 | c.7970A>T (p.Lys2657Ile) c.7601A>T (p.Lys2534Ile) c.437A>T (p.Lys146Ile) c.7978A>T (n.7978A>T) c.535A>T c.7874A>T (p.Lys2625Ile) | |
| 13 | g.32362688A= | CA2082832265 | BRCA2 | c.7971A= (p.Lys2657=) c.7602A= (p.Lys2534=) c.438A= (p.Lys146=) c.7979A= (n.7979A=) c.536A= c.7875A= (p.Lys2625=) | |
| 13 | g.32362688A>C | CA387747340 | BRCA2 | c.7971A>C (p.Lys2657Asn) c.7602A>C (p.Lys2534Asn) c.438A>C (p.Lys146Asn) c.7979A>C (n.7979A>C) c.536A>C c.7875A>C (p.Lys2625Asn) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32362688A>G | CA338244 | BRCA2 | c.7971A>G (p.Lys2657=) c.7602A>G (p.Lys2534=) c.438A>G (p.Lys146=) c.7979A>G (n.7979A>G) c.536A>G c.7875A>G (p.Lys2625=) | ClinVar dbSNP |
| 13 | g.32362688A>T | CA387747341 | BRCA2 | c.7971A>T (p.Lys2657Asn) c.7602A>T (p.Lys2534Asn) c.438A>T (p.Lys146Asn) c.7979A>T (n.7979A>T) c.536A>T c.7875A>T (p.Lys2625Asn) | dbSNP |
| 13 | g.32362689T>A | CA387747344 | BRCA2 | c.7972T>A (p.Tyr2658Asn) c.7603T>A (p.Tyr2535Asn) c.439T>A (p.Tyr147Asn) c.7980T>A (n.7980T>A) c.537T>A c.7876T>A (p.Tyr2626Asn) | dbSNP |
| 13 | g.32362689T>C | CA025360 | BRCA2 | c.7972T>C (p.Tyr2658His) c.7603T>C (p.Tyr2535His) c.439T>C (p.Tyr147His) c.7980T>C (n.7980T>C) c.537T>C c.7876T>C (p.Tyr2626His) | ClinVar dbSNP |
| 13 | g.32362689T>G | CA387747347 | BRCA2 | c.7972T>G (p.Tyr2658Asp) c.7603T>G (p.Tyr2535Asp) c.439T>G (p.Tyr147Asp) c.7980T>G (n.7980T>G) c.537T>G c.7876T>G (p.Tyr2626Asp) | |
| 13 | g.32362689T= | CA2082832272 | BRCA2 | c.7972T= (p.Tyr2658=) c.7603T= (p.Tyr2535=) c.439T= (p.Tyr147=) c.7980T= (n.7980T=) c.537T= c.7876T= (p.Tyr2626=) | |
| 13 | g.32362690A= | CA2082832288 | BRCA2 | c.7973A= (p.Tyr2658=) c.7604A= (p.Tyr2535=) c.440A= (p.Tyr147=) c.7981A= (n.7981A=) c.538A= c.7877A= (p.Tyr2626=) | |
| 13 | g.32362690A>C | CA387747351 | BRCA2 | c.7973A>C (p.Tyr2658Ser) c.7604A>C (p.Tyr2535Ser) c.440A>C (p.Tyr147Ser) c.7981A>C (n.7981A>C) c.538A>C c.7877A>C (p.Tyr2626Ser) | dbSNP |
| 13 | g.32362690A>G | CA387747356 | BRCA2 | c.7973A>G (p.Tyr2658Cys) c.7604A>G (p.Tyr2535Cys) c.440A>G (p.Tyr147Cys) c.7981A>G (n.7981A>G) c.538A>G c.7877A>G (p.Tyr2626Cys) | ClinVar dbSNP |
| 13 | g.32362690A>T | CA387747353 | BRCA2 | c.7973A>T (p.Tyr2658Phe) c.7604A>T (p.Tyr2535Phe) c.440A>T (p.Tyr147Phe) c.7981A>T (n.7981A>T) c.538A>T c.7877A>T (p.Tyr2626Phe) | dbSNP |
| 13 | g.32362691C>A | CA10589460 | BRCA2 | c.7974C>A (p.Tyr2658Ter) c.7605C>A (p.Tyr2535Ter) c.441C>A (p.Tyr147Ter) c.7982C>A (n.7982C>A) c.539C>A c.7878C>A (p.Tyr2626Ter) | ClinVar dbSNP |
| 13 | g.32362691C= | CA2082832305 | BRCA2 | c.7974C= (p.Tyr2658=) c.7605C= (p.Tyr2535=) c.441C= (p.Tyr147=) c.7982C= (n.7982C=) c.539C= c.7878C= (p.Tyr2626=) | |
| 13 | g.32362691C>G | CA025361 | BRCA2 | c.7974C>G (p.Tyr2658Ter) c.7605C>G (p.Tyr2535Ter) c.441C>G (p.Tyr147Ter) c.7982C>G (n.7982C>G) c.539C>G c.7878C>G (p.Tyr2626Ter) | ClinVar dbSNP |
| 13 | g.32362691C>T | CA483261063 | BRCA2 | c.7974C>T (p.Tyr2658=) c.7605C>T (p.Tyr2535=) c.441C>T (p.Tyr147=) c.7982C>T (n.7982C>T) c.539C>T c.7878C>T (p.Tyr2626=) | ClinVar dbSNP |
| 13 | g.32362692A= | CA2082832327 | BRCA2 | c.7975A= (p.Arg2659=) c.7606A= (p.Arg2536=) c.442A= (p.Arg148=) c.7983A= (n.7983A=) c.540A= c.7879A= (p.Arg2627=) | |
| 13 | g.32362692A>C | CA483261064 | BRCA2 | c.7975A>C (p.Arg2659=) c.7606A>C (p.Arg2536=) c.442A>C (p.Arg148=) c.7983A>C (n.7983A>C) c.540A>C c.7879A>C (p.Arg2627=) | dbSNP |
| 13 | g.32362692A>G | CA025362 | BRCA2 | c.7975A>G (p.Arg2659Gly) c.7606A>G (p.Arg2536Gly) c.442A>G (p.Arg148Gly) c.7983A>G (n.7983A>G) c.540A>G c.7879A>G (p.Arg2627Gly) | ClinVar dbSNP gnomAD v4 |
| 13 | g.32362692A>T | CA387747363 | BRCA2 | c.7975A>T (p.Arg2659Ter) c.7606A>T (p.Arg2536Ter) c.442A>T (p.Arg148Ter) c.7983A>T (n.7983A>T) c.540A>T c.7879A>T (p.Arg2627Ter) | |
| 13 | g.32362693G>A | CA025368 | BRCA2 | c.7976G>A (p.Arg2659Lys) c.7607G>A (p.Arg2536Lys) c.443G>A (p.Arg148Lys) c.7984G>A (n.7984G>A) c.541G>A c.7880G>A (p.Arg2627Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32362693G>C | CA025369 | BRCA2 | c.7976G>C (p.Arg2659Thr) c.7607G>C (p.Arg2536Thr) c.443G>C (p.Arg148Thr) c.7984G>C (n.7984G>C) c.541G>C c.7880G>C (p.Arg2627Thr) | ClinVar dbSNP |
| 13 | g.32362693G= | CA2082832336 | BRCA2 | c.7976G= (p.Arg2659=) c.7607G= (p.Arg2536=) c.443G= (p.Arg148=) c.7984G= (n.7984G=) c.541G= c.7880G= (p.Arg2627=) | |
| 13 | g.32362693G>T | CA387747368 | BRCA2 | c.7976G>T (p.Arg2659Ile) c.7607G>T (p.Arg2536Ile) c.443G>T (p.Arg148Ile) c.7984G>T (n.7984G>T) c.541G>T c.7880G>T (p.Arg2627Ile) | ClinVar dbSNP |
| 13 | g.32362694G>A | CA025364 | BRCA2 | c.7976+1G>A (n.7976+1G>A) c.7607+1G>A (n.7607+1G>A) c.443+1G>A (n.443+1G>A) c.7984+1G>A (n.7984+1G>A) c.541+1G>A c.7880+1G>A (n.7880+1G>A) | ClinVar dbSNP |
| 13 | g.32362694G>C | CA387747372 | BRCA2 | c.7976+1G>C (n.7976+1G>C) c.7607+1G>C (n.7607+1G>C) c.443+1G>C (n.443+1G>C) c.7984+1G>C (n.7984+1G>C) c.541+1G>C c.7880+1G>C (n.7880+1G>C) | dbSNP |
| 13 | g.32362694G= | CA2082832350 | BRCA2 | c.7976+1G= (n.7976+1G=) c.7607+1G= (n.7607+1G=) c.443+1G= (n.443+1G=) c.7984+1G= (n.7984+1G=) c.541+1G= c.7880+1G= (n.7880+1G=) | |
| 13 | g.32362694G>T | CA387747374 | BRCA2 | c.7976+1G>T (n.7976+1G>T) c.7607+1G>T (n.7607+1G>T) c.443+1G>T (n.443+1G>T) c.7984+1G>T (n.7984+1G>T) c.541+1G>T c.7880+1G>T (n.7880+1G>T) | ClinVar dbSNP |
| 13 | g.32362695C>A | CA10602543 | BRCA2 | c.7976+2C>A (n.7976+2C>A) c.7607+2C>A (n.7607+2C>A) c.443+2C>A (n.443+2C>A) c.7984+2C>A (n.7984+2C>A) c.541+2C>A c.7880+2C>A (n.7880+2C>A) | ClinVar dbSNP |
| 13 | g.32362695C= | CA2082832361 | BRCA2 | c.7976+2C= (n.7976+2C=) c.7607+2C= (n.7607+2C=) c.443+2C= (n.443+2C=) c.7984+2C= (n.7984+2C=) c.541+2C= c.7880+2C= (n.7880+2C=) | |
| 13 | g.32362695C>G | CA16619774 | BRCA2 | c.7976+2C>G (n.7976+2C>G) c.7607+2C>G (n.7607+2C>G) c.443+2C>G (n.443+2C>G) c.7984+2C>G (n.7984+2C>G) c.541+2C>G c.7880+2C>G (n.7880+2C>G) | ClinVar dbSNP |
| 13 | g.32362695C>T | CA387747377 | BRCA2 | c.7976+2C>T (n.7976+2C>T) c.7607+2C>T (n.7607+2C>T) c.443+2C>T (n.443+2C>T) c.7984+2C>T (n.7984+2C>T) c.541+2C>T c.7880+2C>T (n.7880+2C>T) | dbSNP gnomAD v4 |
| 13 | g.32362695_32362697delinsCAA | CA2082832359 | BRCA2 | c.7976+2_7976+4delinsCAA (n.7976+2_7976+4delinsCAA) c.7607+2_7607+4delinsCAA (n.7607+2_7607+4delinsCAA) c.443+2_443+4delinsCAA (n.443+2_443+4delinsCAA) c.7984+2_7984+4delinsCAA (n.7984+2_7984+4delinsCAA) c.541+2_541+4delinsCAA c.7880+2_7880+4delinsCAA (n.7880+2_7880+4delinsCAA) | |
| 13 | g.32362696A= | CA2082832370 | BRCA2 | c.7976+3A= (n.7976+3A=) c.7607+3A= (n.7607+3A=) c.443+3A= (n.443+3A=) c.7984+3A= (n.7984+3A=) c.541+3A= c.7880+3A= (n.7880+3A=) | |
| 13 | g.32362696A>C | CA658653813 | BRCA2 | c.7976+3A>C (n.7976+3A>C) c.7607+3A>C (n.7607+3A>C) c.443+3A>C (n.443+3A>C) c.7984+3A>C (n.7984+3A>C) c.541+3A>C c.7880+3A>C (n.7880+3A>C) | ClinVar dbSNP |
| 13 | g.32362696A>G | CA2727873208 | BRCA2 | c.7976+3A>G (n.7976+3A>G) c.7607+3A>G (n.7607+3A>G) c.443+3A>G (n.443+3A>G) c.7984+3A>G (n.7984+3A>G) c.541+3A>G c.7880+3A>G (n.7880+3A>G) | dbSNP |
| 13 | g.32362696A>T | CA2727873209 | BRCA2 | c.7976+3A>T (n.7976+3A>T) c.7607+3A>T (n.7607+3A>T) c.443+3A>T (n.443+3A>T) c.7984+3A>T (n.7984+3A>T) c.541+3A>T c.7880+3A>T (n.7880+3A>T) | dbSNP |
| 13 | g.32362696_32362697del | CA025366 | BRCA2 | c.7976+3_7976+4del (n.7976+3_7976+4del) c.7607+3_7607+4del (n.7607+3_7607+4del) c.443+3_443+4del (n.443+3_443+4del) c.7984+3_7984+4del (n.7984+3_7984+4del) c.541+3_541+4del c.7880+3_7880+4del (n.7880+3_7880+4del) | ClinVar dbSNP |
| 13 | g.32362697A= | CA2082832375 | BRCA2 | c.7976+4A= (n.7976+4A=) c.7607+4A= (n.7607+4A=) c.443+4A= (n.443+4A=) c.7984+4A= (n.7984+4A=) c.541+4A= c.7880+4A= (n.7880+4A=) | |
| 13 | g.32362697A>C | CA658656487 | BRCA2 | c.7976+4A>C (n.7976+4A>C) c.7607+4A>C (n.7607+4A>C) c.443+4A>C (n.443+4A>C) c.7984+4A>C (n.7984+4A>C) c.541+4A>C c.7880+4A>C (n.7880+4A>C) | ClinVar dbSNP |
| 13 | g.32362697A>G | CA10579762 | BRCA2 | c.7976+4A>G (n.7976+4A>G) c.7607+4A>G (n.7607+4A>G) c.443+4A>G (n.443+4A>G) c.7984+4A>G (n.7984+4A>G) c.541+4A>G c.7880+4A>G (n.7880+4A>G) | ClinVar dbSNP gnomAD v4 |
| 13 | g.32362697A>T | CA2727841632 | BRCA2 | c.7976+4A>T (n.7976+4A>T) c.7607+4A>T (n.7607+4A>T) c.443+4A>T (n.443+4A>T) c.7984+4A>T (n.7984+4A>T) c.541+4A>T c.7880+4A>T (n.7880+4A>T) | dbSNP |
| 13 | g.32362698G>A | CA025367 | BRCA2 | c.7976+5G>A (n.7976+5G>A) c.7607+5G>A (n.7607+5G>A) c.443+5G>A (n.443+5G>A) c.7984+5G>A (n.7984+5G>A) c.541+5G>A c.7880+5G>A (n.7880+5G>A) | ClinVar dbSNP gnomAD v4 |
| 13 | g.32362698G>C | CA609091813 | BRCA2 | c.7976+5G>C (n.7976+5G>C) c.7607+5G>C (n.7607+5G>C) c.443+5G>C (n.443+5G>C) c.7984+5G>C (n.7984+5G>C) c.541+5G>C c.7880+5G>C (n.7880+5G>C) | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32362698G= | CA2082832392 | BRCA2 | c.7976+5G= (n.7976+5G=) c.7607+5G= (n.7607+5G=) c.443+5G= (n.443+5G=) c.7984+5G= (n.7984+5G=) c.541+5G= c.7880+5G= (n.7880+5G=) | |
| 13 | g.32362698G>T | CA658656488 | BRCA2 | c.7976+5G>T (n.7976+5G>T) c.7607+5G>T (n.7607+5G>T) c.443+5G>T (n.443+5G>T) c.7984+5G>T (n.7984+5G>T) c.541+5G>T c.7880+5G>T (n.7880+5G>T) | ClinVar dbSNP |
| 13 | g.32362699T>A | CA2727917464 | BRCA2 | c.7976+6T>A (n.7976+6T>A) c.7607+6T>A (n.7607+6T>A) c.443+6T>A (n.443+6T>A) c.7984+6T>A (n.7984+6T>A) c.541+6T>A c.7880+6T>A (n.7880+6T>A) | dbSNP |
| 13 | g.32362701dup | CA2839550516 | BRCA2 | c.7976+8dup (n.7976+8dup) c.7607+8dup (n.7607+8dup) c.443+8dup (n.443+8dup) c.7984+8dup (n.7984+8dup) c.541+8dup c.7880+8dup (n.7880+8dup) | |
| 13 | g.32362700T>A | CA2499222316 | BRCA2 | c.7976+7T>A (n.7976+7T>A) c.7607+7T>A (n.7607+7T>A) c.443+7T>A (n.443+7T>A) c.7984+7T>A (n.7984+7T>A) c.541+7T>A c.7880+7T>A (n.7880+7T>A) | ClinVar dbSNP |
| 13 | g.32362700T>C | CA915946884 | BRCA2 | c.7976+7T>C (n.7976+7T>C) c.7607+7T>C (n.7607+7T>C) c.443+7T>C (n.443+7T>C) c.7984+7T>C (n.7984+7T>C) c.541+7T>C c.7880+7T>C (n.7880+7T>C) | ClinVar dbSNP |
| 13 | g.32362700T= | CA2082832406 | BRCA2 | c.7976+7T= (n.7976+7T=) c.7607+7T= (n.7607+7T=) c.443+7T= (n.443+7T=) c.7984+7T= (n.7984+7T=) c.541+7T= c.7880+7T= (n.7880+7T=) | |
| 13 | g.32362701T>A | CA2727917468 | BRCA2 | c.7976+8T>A (n.7976+8T>A) c.7607+8T>A (n.7607+8T>A) c.443+8T>A (n.443+8T>A) c.7984+8T>A (n.7984+8T>A) c.541+8T>A c.7880+8T>A (n.7880+8T>A) | dbSNP |
| 13 | g.32362701_32362702delinsTA | CA2082832408 | BRCA2 | c.7976+8_7976+9delinsTA (n.7976+8_7976+9delinsTA) c.7607+8_7607+9delinsTA (n.7607+8_7607+9delinsTA) c.443+8_443+9delinsTA (n.443+8_443+9delinsTA) c.7984+8_7984+9delinsTA (n.7984+8_7984+9delinsTA) c.541+8_541+9delinsTA c.7880+8_7880+9delinsTA (n.7880+8_7880+9delinsTA) | |
| 13 | g.32362702A= | CA2082832413 | BRCA2 | c.7976+9A= (n.7976+9A=) c.7607+9A= (n.7607+9A=) c.443+9A= (n.443+9A=) c.7984+9A= (n.7984+9A=) c.541+9A= c.7880+9A= (n.7880+9A=) | |
| 13 | g.32362702A>C | CA2580087439 | BRCA2 | c.7976+9A>C (n.7976+9A>C) c.7607+9A>C (n.7607+9A>C) c.443+9A>C (n.443+9A>C) c.7984+9A>C (n.7984+9A>C) c.541+9A>C c.7880+9A>C (n.7880+9A>C) | ClinVar |
| 13 | g.32362702A>G | CA2082832412 | BRCA2 | c.7976+9A>G (n.7976+9A>G) c.7607+9A>G (n.7607+9A>G) c.443+9A>G (n.443+9A>G) c.7984+9A>G (n.7984+9A>G) c.541+9A>G c.7880+9A>G (n.7880+9A>G) | dbSNP |
| 13 | g.32362704del | CA6941164 | BRCA2 | c.7976+11del (n.7976+11del) c.7607+11del (n.7607+11del) c.443+11del (n.443+11del) c.7984+11del (n.7984+11del) c.541+11del c.7880+11del (n.7880+11del) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32362703A= | CA2082832432 | BRCA2 | c.7976+10A= (n.7976+10A=) c.7607+10A= (n.7607+10A=) c.443+10A= (n.443+10A=) c.7984+10A= (n.7984+10A=) c.541+10A= c.7880+10A= (n.7880+10A=) | |
| 13 | g.32362703A>G | CA2727874192 | BRCA2 | c.7976+10A>G (n.7976+10A>G) c.7607+10A>G (n.7607+10A>G) c.443+10A>G (n.443+10A>G) c.7984+10A>G (n.7984+10A>G) c.541+10A>G c.7880+10A>G (n.7880+10A>G) | dbSNP |
| 13 | g.32362703A>T | CA913188565 | BRCA2 | c.7976+10A>T (n.7976+10A>T) c.7607+10A>T (n.7607+10A>T) c.443+10A>T (n.443+10A>T) c.7984+10A>T (n.7984+10A>T) c.541+10A>T c.7880+10A>T (n.7880+10A>T) | ClinVar dbSNP |
| 13 | g.32362704A= | CA2082832436 | BRCA2 | c.7976+11A= (n.7976+11A=) c.7607+11A= (n.7607+11A=) c.443+11A= (n.443+11A=) c.7984+11A= (n.7984+11A=) c.541+11A= c.7880+11A= (n.7880+11A=) | |
| 13 | g.32362704A>C | CA658798127 | BRCA2 | c.7976+11A>C (n.7976+11A>C) c.7607+11A>C (n.7607+11A>C) c.443+11A>C (n.443+11A>C) c.7984+11A>C (n.7984+11A>C) c.541+11A>C c.7880+11A>C (n.7880+11A>C) | ClinVar dbSNP |
| 13 | g.32362705G>A | CA025363 | BRCA2 | c.7976+12G>A (n.7976+12G>A) c.7607+12G>A (n.7607+12G>A) c.443+12G>A (n.443+12G>A) c.7984+12G>A (n.7984+12G>A) c.541+12G>A c.7880+12G>A (n.7880+12G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32362705G>C | CA2838169167 | BRCA2 | c.7976+12G>C (n.7976+12G>C) c.7607+12G>C (n.7607+12G>C) c.443+12G>C (n.443+12G>C) c.7984+12G>C (n.7984+12G>C) c.541+12G>C c.7880+12G>C (n.7880+12G>C) | |
| 13 | g.32362705G= | CA2082832444 | BRCA2 | c.7976+12G= (n.7976+12G=) c.7607+12G= (n.7607+12G=) c.443+12G= (n.443+12G=) c.7984+12G= (n.7984+12G=) c.541+12G= c.7880+12G= (n.7880+12G=) | |
| 13 | g.32362705G>T | CA2838169166 | BRCA2 | c.7976+12G>T (n.7976+12G>T) c.7607+12G>T (n.7607+12G>T) c.443+12G>T (n.443+12G>T) c.7984+12G>T (n.7984+12G>T) c.541+12G>T c.7880+12G>T (n.7880+12G>T) | |
| 13 | g.32362706C>G | CA2727917474 | BRCA2 | c.7976+13C>G (n.7976+13C>G) c.7607+13C>G (n.7607+13C>G) c.443+13C>G (n.443+13C>G) c.7984+13C>G (n.7984+13C>G) c.541+13C>G c.7880+13C>G (n.7880+13C>G) | dbSNP |
| 13 | g.32362706C>T | CA2697551755 | BRCA2 | c.7976+13C>T (n.7976+13C>T) c.7607+13C>T (n.7607+13C>T) c.443+13C>T (n.443+13C>T) c.7984+13C>T (n.7984+13C>T) c.541+13C>T c.7880+13C>T (n.7880+13C>T) | ClinVar dbSNP |
| 13 | g.32362707A= | CA2082832448 | BRCA2 | c.7976+14A= (n.7976+14A=) c.7607+14A= (n.7607+14A=) c.443+14A= (n.443+14A=) c.7984+14A= (n.7984+14A=) c.541+14A= c.7880+14A= (n.7880+14A=) | |
| 13 | g.32362707A>G | CA6941165 | BRCA2 | c.7976+14A>G (n.7976+14A>G) c.7607+14A>G (n.7607+14A>G) c.443+14A>G (n.443+14A>G) c.7984+14A>G (n.7984+14A>G) c.541+14A>G c.7880+14A>G (n.7880+14A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32362708T>A | CA2727917495 | BRCA2 | c.7976+15T>A (n.7976+15T>A) c.7607+15T>A (n.7607+15T>A) c.443+15T>A (n.443+15T>A) c.7984+15T>A (n.7984+15T>A) c.541+15T>A c.7880+15T>A (n.7880+15T>A) | dbSNP |
| 13 | g.32362709T>A | CA2727917516 | BRCA2 | c.7976+16T>A (n.7976+16T>A) c.7607+16T>A (n.7607+16T>A) c.443+16T>A (n.443+16T>A) c.7984+16T>A (n.7984+16T>A) c.541+16T>A c.7880+16T>A (n.7880+16T>A) | dbSNP |
| 13 | g.32362709T>C | CA2727917510 | BRCA2 | c.7976+16T>C (n.7976+16T>C) c.7607+16T>C (n.7607+16T>C) c.443+16T>C (n.443+16T>C) c.7984+16T>C (n.7984+16T>C) c.541+16T>C c.7880+16T>C (n.7880+16T>C) | dbSNP |
| 13 | g.32362710A= | CA2082832455 | BRCA2 | c.7976+17A= (n.7976+17A=) c.7607+17A= (n.7607+17A=) c.443+17A= (n.443+17A=) c.7984+17A= (n.7984+17A=) c.541+17A= c.7880+17A= (n.7880+17A=) | |
| 13 | g.32362710A>G | CA6941166 | BRCA2 | c.7976+17A>G (n.7976+17A>G) c.7607+17A>G (n.7607+17A>G) c.443+17A>G (n.443+17A>G) c.7984+17A>G (n.7984+17A>G) c.541+17A>G c.7880+17A>G (n.7880+17A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32362710A>T | CA2727839134 | BRCA2 | c.7976+17A>T (n.7976+17A>T) c.7607+17A>T (n.7607+17A>T) c.443+17A>T (n.443+17A>T) c.7984+17A>T (n.7984+17A>T) c.541+17A>T c.7880+17A>T (n.7880+17A>T) | dbSNP |
| 13 | g.32362711C>A | CA609091814 | BRCA2 | c.7976+18C>A (n.7976+18C>A) c.7607+18C>A (n.7607+18C>A) c.443+18C>A (n.443+18C>A) c.7984+18C>A (n.7984+18C>A) c.541+18C>A c.7880+18C>A (n.7880+18C>A) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32362711C= | CA2082832466 | BRCA2 | c.7976+18C= (n.7976+18C=) c.7607+18C= (n.7607+18C=) c.443+18C= (n.443+18C=) c.7984+18C= (n.7984+18C=) c.541+18C= c.7880+18C= (n.7880+18C=) | |
| 13 | g.32362711C>G | CA2727853389 | BRCA2 | c.7976+18C>G (n.7976+18C>G) c.7607+18C>G (n.7607+18C>G) c.443+18C>G (n.443+18C>G) c.7984+18C>G (n.7984+18C>G) c.541+18C>G c.7880+18C>G (n.7880+18C>G) | dbSNP |
| 13 | g.32362711C>T | CA16606819 | BRCA2 | c.7976+18C>T (n.7976+18C>T) c.7607+18C>T (n.7607+18C>T) c.443+18C>T (n.443+18C>T) c.7984+18C>T (n.7984+18C>T) c.541+18C>T c.7880+18C>T (n.7880+18C>T) | ClinVar dbSNP |
| 13 | g.32362712A= | CA2082832482 | BRCA2 | c.7976+19A= (n.7976+19A=) c.7607+19A= (n.7607+19A=) c.443+19A= (n.443+19A=) c.7984+19A= (n.7984+19A=) c.541+19A= c.7880+19A= (n.7880+19A=) | |
| 13 | g.32362712A>G | CA658798128 | BRCA2 | c.7976+19A>G (n.7976+19A>G) c.7607+19A>G (n.7607+19A>G) c.443+19A>G (n.443+19A>G) c.7984+19A>G (n.7984+19A>G) c.541+19A>G c.7880+19A>G (n.7880+19A>G) | ClinVar dbSNP gnomAD v4 |
| 13 | g.32362712A>T | CA2082832493 | BRCA2 | c.7976+19A>T (n.7976+19A>T) c.7607+19A>T (n.7607+19A>T) c.443+19A>T (n.443+19A>T) c.7984+19A>T (n.7984+19A>T) c.541+19A>T c.7880+19A>T (n.7880+19A>T) | dbSNP |
| 13 | g.32362713T>A | CA2727917577 | BRCA2 | c.7976+20T>A (n.7976+20T>A) c.7607+20T>A (n.7607+20T>A) c.443+20T>A (n.443+20T>A) c.7984+20T>A (n.7984+20T>A) c.541+20T>A c.7880+20T>A (n.7880+20T>A) | dbSNP |
| 13 | g.32362713T>C | CA2727917579 | BRCA2 | c.7976+20T>C (n.7976+20T>C) c.7607+20T>C (n.7607+20T>C) c.443+20T>C (n.443+20T>C) c.7984+20T>C (n.7984+20T>C) c.541+20T>C c.7880+20T>C (n.7880+20T>C) | dbSNP |
| 13 | g.32362714T>A | CA2727839874 | BRCA2 | c.7976+21T>A (n.7976+21T>A) c.7607+21T>A (n.7607+21T>A) c.443+21T>A (n.443+21T>A) c.7984+21T>A (n.7984+21T>A) c.541+21T>A c.7880+21T>A (n.7880+21T>A) | dbSNP |
| 13 | g.32362714T>G | CA6941167 | BRCA2 | c.7976+21T>G (n.7976+21T>G) c.7607+21T>G (n.7607+21T>G) c.443+21T>G (n.443+21T>G) c.7984+21T>G (n.7984+21T>G) c.541+21T>G c.7880+21T>G (n.7880+21T>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32362714T= | CA2082832499 | BRCA2 | c.7976+21T= (n.7976+21T=) c.7607+21T= (n.7607+21T=) c.443+21T= (n.443+21T=) c.7984+21T= (n.7984+21T=) c.541+21T= c.7880+21T= (n.7880+21T=) | |
| 13 | g.32362715A>T | CA2727917697 | BRCA2 | c.7976+22A>T (n.7976+22A>T) c.7607+22A>T (n.7607+22A>T) c.443+22A>T (n.443+22A>T) c.7984+22A>T (n.7984+22A>T) c.541+22A>T c.7880+22A>T (n.7880+22A>T) | dbSNP |
| 13 | g.32362716C>A | CA6941168 | BRCA2 | c.7976+23C>A (n.7976+23C>A) c.7607+23C>A (n.7607+23C>A) c.443+23C>A (n.443+23C>A) c.7984+23C>A (n.7984+23C>A) c.541+23C>A c.7880+23C>A (n.7880+23C>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32362716C= | CA2082832507 | BRCA2 | c.7976+23C= (n.7976+23C=) c.7607+23C= (n.7607+23C=) c.443+23C= (n.443+23C=) c.7984+23C= (n.7984+23C=) c.541+23C= c.7880+23C= (n.7880+23C=) | |
| 13 | g.32362716C>G | CA10576073 | BRCA2 | c.7976+23C>G (n.7976+23C>G) c.7607+23C>G (n.7607+23C>G) c.443+23C>G (n.443+23C>G) c.7984+23C>G (n.7984+23C>G) c.541+23C>G c.7880+23C>G (n.7880+23C>G) | ClinVar dbSNP |
| 13 | g.32362716C>T | CA025365 | BRCA2 | c.7976+23C>T (n.7976+23C>T) c.7607+23C>T (n.7607+23C>T) c.443+23C>T (n.443+23C>T) c.7984+23C>T (n.7984+23C>T) c.541+23C>T c.7880+23C>T (n.7880+23C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32362717G>A | CA6941169 | BRCA2 | c.7976+24G>A (n.7976+24G>A) c.7607+24G>A (n.7607+24G>A) c.443+24G>A (n.443+24G>A) c.7984+24G>A (n.7984+24G>A) c.541+24G>A c.7880+24G>A (n.7880+24G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32362717G>C | CA2727835703 | BRCA2 | c.7976+24G>C (n.7976+24G>C) c.7607+24G>C (n.7607+24G>C) c.443+24G>C (n.443+24G>C) c.7984+24G>C (n.7984+24G>C) c.541+24G>C c.7880+24G>C (n.7880+24G>C) | dbSNP |
| 13 | g.32362717G= | CA2082832513 | BRCA2 | c.7976+24G= (n.7976+24G=) c.7607+24G= (n.7607+24G=) c.443+24G= (n.443+24G=) c.7984+24G= (n.7984+24G=) c.541+24G= c.7880+24G= (n.7880+24G=) | |
| 13 | g.32362718T>A | CA2622572913 | BRCA2 | c.7976+25T>A (n.7976+25T>A) c.7607+25T>A (n.7607+25T>A) c.443+25T>A (n.443+25T>A) c.7984+25T>A (n.7984+25T>A) c.541+25T>A c.7880+25T>A (n.7880+25T>A) | gnomAD v4 |
| 13 | g.32362719A= | CA2082832519 | BRCA2 | c.7976+26A= (n.7976+26A=) c.7607+26A= (n.7607+26A=) c.443+26A= (n.443+26A=) c.7984+26A= (n.7984+26A=) c.541+26A= c.7880+26A= (n.7880+26A=) | |
| 13 | g.32362719A>C | CA2082832520 | BRCA2 | c.7976+26A>C (n.7976+26A>C) c.7607+26A>C (n.7607+26A>C) c.443+26A>C (n.443+26A>C) c.7984+26A>C (n.7984+26A>C) c.541+26A>C c.7880+26A>C (n.7880+26A>C) | dbSNP |
| 13 | g.32362720A>G | CA2622572914 | BRCA2 | c.7976+27A>G (n.7976+27A>G) c.7607+27A>G (n.7607+27A>G) c.443+27A>G (n.443+27A>G) c.7984+27A>G (n.7984+27A>G) c.541+27A>G c.7880+27A>G (n.7880+27A>G) | gnomAD v4 |
| 13 | g.32362720A>T | CA2727917698 | BRCA2 | c.7976+27A>T (n.7976+27A>T) c.7607+27A>T (n.7607+27A>T) c.443+27A>T (n.443+27A>T) c.7984+27A>T (n.7984+27A>T) c.541+27A>T c.7880+27A>T (n.7880+27A>T) | dbSNP |
| 13 | g.32362722C>A | CA2727917737 | BRCA2 | c.7976+29C>A (n.7976+29C>A) c.7607+29C>A (n.7607+29C>A) c.443+29C>A (n.443+29C>A) c.7984+29C>A (n.7984+29C>A) c.541+29C>A c.7880+29C>A (n.7880+29C>A) | dbSNP |
| 13 | g.32362722C>G | CA2727917736 | BRCA2 | c.7976+29C>G (n.7976+29C>G) c.7607+29C>G (n.7607+29C>G) c.443+29C>G (n.443+29C>G) c.7984+29C>G (n.7984+29C>G) c.541+29C>G c.7880+29C>G (n.7880+29C>G) | dbSNP |
| 13 | g.32362722C>T | CA2727917715 | BRCA2 | c.7976+29C>T (n.7976+29C>T) c.7607+29C>T (n.7607+29C>T) c.443+29C>T (n.443+29C>T) c.7984+29C>T (n.7984+29C>T) c.541+29C>T c.7880+29C>T (n.7880+29C>T) | dbSNP |
| 13 | g.32362723A= | CA2082832521 | BRCA2 | c.7976+30A= (n.7976+30A=) c.7607+30A= (n.7607+30A=) c.443+30A= (n.443+30A=) c.7984+30A= (n.7984+30A=) c.541+30A= c.7880+30A= (n.7880+30A=) | |
| 13 | g.32362723A>G | CA697355342 | BRCA2 | c.7976+30A>G (n.7976+30A>G) c.7607+30A>G (n.7607+30A>G) c.443+30A>G (n.443+30A>G) c.7984+30A>G (n.7984+30A>G) c.541+30A>G c.7880+30A>G (n.7880+30A>G) | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32362724T>A | CA2727917774 | BRCA2 | c.7976+31T>A (n.7976+31T>A) c.7607+31T>A (n.7607+31T>A) c.443+31T>A (n.443+31T>A) c.7984+31T>A (n.7984+31T>A) c.541+31T>A c.7880+31T>A (n.7880+31T>A) | dbSNP |
| 13 | g.32362724T>C | CA2727917752 | BRCA2 | c.7976+31T>C (n.7976+31T>C) c.7607+31T>C (n.7607+31T>C) c.443+31T>C (n.443+31T>C) c.7984+31T>C (n.7984+31T>C) c.541+31T>C c.7880+31T>C (n.7880+31T>C) | dbSNP |
| 13 | g.32362726T>A | CA2727874193 | BRCA2 | c.7976+33T>A (n.7976+33T>A) c.7607+33T>A (n.7607+33T>A) c.443+33T>A (n.443+33T>A) c.7984+33T>A (n.7984+33T>A) c.541+33T>A c.7880+33T>A (n.7880+33T>A) | dbSNP |
| 13 | g.32362726T>C | CA2082832525 | BRCA2 | c.7976+33T>C (n.7976+33T>C) c.7607+33T>C (n.7607+33T>C) c.443+33T>C (n.443+33T>C) c.7984+33T>C (n.7984+33T>C) c.541+33T>C c.7880+33T>C (n.7880+33T>C) | dbSNP |
| 13 | g.32362726T>G | CA2622572915 | BRCA2 | c.7976+33T>G (n.7976+33T>G) c.7607+33T>G (n.7607+33T>G) c.443+33T>G (n.443+33T>G) c.7984+33T>G (n.7984+33T>G) c.541+33T>G c.7880+33T>G (n.7880+33T>G) | gnomAD v4 |
| 13 | g.32362726T= | CA2082832524 | BRCA2 | c.7976+33T= (n.7976+33T=) c.7607+33T= (n.7607+33T=) c.443+33T= (n.443+33T=) c.7984+33T= (n.7984+33T=) c.541+33T= c.7880+33T= (n.7880+33T=) | |
| 13 | g.32362727A>T | CA2727917777 | BRCA2 | c.7976+34A>T (n.7976+34A>T) c.7607+34A>T (n.7607+34A>T) c.443+34A>T (n.443+34A>T) c.7984+34A>T (n.7984+34A>T) c.541+34A>T c.7880+34A>T (n.7880+34A>T) | dbSNP |
| 13 | g.32362728C>A | CA6941170 | BRCA2 | c.7976+35C>A (n.7976+35C>A) c.7607+35C>A (n.7607+35C>A) c.443+35C>A (n.443+35C>A) c.7984+35C>A (n.7984+35C>A) c.541+35C>A c.7880+35C>A (n.7880+35C>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32362728C= | CA2082832536 | BRCA2 | c.7976+35C= (n.7976+35C=) c.7607+35C= (n.7607+35C=) c.443+35C= (n.443+35C=) c.7984+35C= (n.7984+35C=) c.541+35C= c.7880+35C= (n.7880+35C=) | |
| 13 | g.32362728C>G | CA2727834943 | BRCA2 | c.7976+35C>G (n.7976+35C>G) c.7607+35C>G (n.7607+35C>G) c.443+35C>G (n.443+35C>G) c.7984+35C>G (n.7984+35C>G) c.541+35C>G c.7880+35C>G (n.7880+35C>G) | dbSNP |
| 13 | g.32362728C>T | CA6941171 | BRCA2 | c.7976+35C>T (n.7976+35C>T) c.7607+35C>T (n.7607+35C>T) c.443+35C>T (n.443+35C>T) c.7984+35C>T (n.7984+35C>T) c.541+35C>T c.7880+35C>T (n.7880+35C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32362729G>A | CA247475401 | BRCA2 | c.7976+36G>A (n.7976+36G>A) c.7607+36G>A (n.7607+36G>A) c.443+36G>A (n.443+36G>A) c.7984+36G>A (n.7984+36G>A) c.541+36G>A c.7880+36G>A (n.7880+36G>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32362729G>C | CA2727836145 | BRCA2 | c.7976+36G>C (n.7976+36G>C) c.7607+36G>C (n.7607+36G>C) c.443+36G>C (n.443+36G>C) c.7984+36G>C (n.7984+36G>C) c.541+36G>C c.7880+36G>C (n.7880+36G>C) | dbSNP |
| 13 | g.32362729G= | CA2082832545 | BRCA2 | c.7976+36G= (n.7976+36G=) c.7607+36G= (n.7607+36G=) c.443+36G= (n.443+36G=) c.7984+36G= (n.7984+36G=) c.541+36G= c.7880+36G= (n.7880+36G=) | |
| 13 | g.32362730G>A | CA609091815 | BRCA2 | c.7976+37G>A (n.7976+37G>A) c.7607+37G>A (n.7607+37G>A) c.443+37G>A (n.443+37G>A) c.7984+37G>A (n.7984+37G>A) c.541+37G>A c.7880+37G>A (n.7880+37G>A) | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32362730G= | CA2082832556 | BRCA2 | c.7976+37G= (n.7976+37G=) c.7607+37G= (n.7607+37G=) c.443+37G= (n.443+37G=) c.7984+37G= (n.7984+37G=) c.541+37G= c.7880+37G= (n.7880+37G=) | |
| 13 | g.32362730G>T | CA2622572916 | BRCA2 | c.7976+37G>T (n.7976+37G>T) c.7607+37G>T (n.7607+37G>T) c.443+37G>T (n.443+37G>T) c.7984+37G>T (n.7984+37G>T) c.541+37G>T c.7880+37G>T (n.7880+37G>T) | gnomAD v4 |
| 13 | g.32362730_32362734del | CA2575388234 | BRCA2 | c.7976+37_7976+41del (n.7976+37_7976+41del) c.7607+37_7607+41del (n.7607+37_7607+41del) c.443+37_443+41del (n.443+37_443+41del) c.7984+37_7984+41del (n.7984+37_7984+41del) c.541+37_541+41del c.7880+37_7880+41del (n.7880+37_7880+41del) | |
| 13 | g.32362731C>A | CA2622572917 | BRCA2 | c.7976+38C>A (n.7976+38C>A) c.7607+38C>A (n.7607+38C>A) c.443+38C>A (n.443+38C>A) c.7984+38C>A (n.7984+38C>A) c.541+38C>A c.7880+38C>A (n.7880+38C>A) | dbSNP gnomAD v4 |
| 13 | g.32362731C>G | CA2727917828 | BRCA2 | c.7976+38C>G (n.7976+38C>G) c.7607+38C>G (n.7607+38C>G) c.443+38C>G (n.443+38C>G) c.7984+38C>G (n.7984+38C>G) c.541+38C>G c.7880+38C>G (n.7880+38C>G) | dbSNP |
| 13 | g.32362731C>T | CA2727917839 | BRCA2 | c.7976+38C>T (n.7976+38C>T) c.7607+38C>T (n.7607+38C>T) c.443+38C>T (n.443+38C>T) c.7984+38C>T (n.7984+38C>T) c.541+38C>T c.7880+38C>T (n.7880+38C>T) | dbSNP |
| 13 | g.32362732A>G | CA2727917863 | BRCA2 | c.7976+39A>G (n.7976+39A>G) c.7607+39A>G (n.7607+39A>G) c.443+39A>G (n.443+39A>G) c.7984+39A>G (n.7984+39A>G) c.541+39A>G c.7880+39A>G (n.7880+39A>G) | dbSNP |
| 13 | g.32362732A>T | CA2727917840 | BRCA2 | c.7976+39A>T (n.7976+39A>T) c.7607+39A>T (n.7607+39A>T) c.443+39A>T (n.443+39A>T) c.7984+39A>T (n.7984+39A>T) c.541+39A>T c.7880+39A>T (n.7880+39A>T) | dbSNP |
| 13 | g.32362733G>A | CA2082832558 | BRCA2 | c.7976+40G>A (n.7976+40G>A) c.7607+40G>A (n.7607+40G>A) c.443+40G>A (n.443+40G>A) c.7984+40G>A (n.7984+40G>A) c.541+40G>A c.7880+40G>A (n.7880+40G>A) | dbSNP |
| 13 | g.32362733G= | CA2082832557 | BRCA2 | c.7976+40G= (n.7976+40G=) c.7607+40G= (n.7607+40G=) c.443+40G= (n.443+40G=) c.7984+40G= (n.7984+40G=) c.541+40G= c.7880+40G= (n.7880+40G=) | |
| 13 | g.32362734T>A | CA2727864197 | BRCA2 | c.7976+41T>A (n.7976+41T>A) c.7607+41T>A (n.7607+41T>A) c.443+41T>A (n.443+41T>A) c.7984+41T>A (n.7984+41T>A) c.541+41T>A c.7880+41T>A (n.7880+41T>A) | dbSNP |
| 13 | g.32362734T>C | CA609091816 | BRCA2 | c.7976+41T>C (n.7976+41T>C) c.7607+41T>C (n.7607+41T>C) c.443+41T>C (n.443+41T>C) c.7984+41T>C (n.7984+41T>C) c.541+41T>C c.7880+41T>C (n.7880+41T>C) | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32362734T= | CA2082832562 | BRCA2 | c.7976+41T= (n.7976+41T=) c.7607+41T= (n.7607+41T=) c.443+41T= (n.443+41T=) c.7984+41T= (n.7984+41T=) c.541+41T= c.7880+41T= (n.7880+41T=) | |
| 13 | g.32362735A= | CA2082832570 | BRCA2 | c.7976+42A= (n.7976+42A=) c.7607+42A= (n.7607+42A=) c.443+42A= (n.443+42A=) c.7984+42A= (n.7984+42A=) c.541+42A= c.7880+42A= (n.7880+42A=) | |
| 13 | g.32362735A>G | CA609091817 | BRCA2 | c.7976+42A>G (n.7976+42A>G) c.7607+42A>G (n.7607+42A>G) c.443+42A>G (n.443+42A>G) c.7984+42A>G (n.7984+42A>G) c.541+42A>G c.7880+42A>G (n.7880+42A>G) | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32362735A>T | CA2727855207 | BRCA2 | c.7976+42A>T (n.7976+42A>T) c.7607+42A>T (n.7607+42A>T) c.443+42A>T (n.443+42A>T) c.7984+42A>T (n.7984+42A>T) c.541+42A>T c.7880+42A>T (n.7880+42A>T) | dbSNP |
| 13 | g.32362736T>A | CA2558562514 | BRCA2 | c.7976+43T>A (n.7976+43T>A) c.7607+43T>A (n.7607+43T>A) c.443+43T>A (n.443+43T>A) c.7984+43T>A (n.7984+43T>A) c.541+43T>A c.7880+43T>A (n.7880+43T>A) | |
| 13 | g.32362737G>A | CA2622572918 | BRCA2 | c.7976+44G>A (n.7976+44G>A) c.7607+44G>A (n.7607+44G>A) c.443+44G>A (n.443+44G>A) c.7984+44G>A (n.7984+44G>A) c.541+44G>A c.7880+44G>A (n.7880+44G>A) | dbSNP gnomAD v4 |
| 13 | g.32362738G>C | CA277582 | BRCA2 | c.7976+45G>C (n.7976+45G>C) c.7607+45G>C (n.7607+45G>C) c.443+45G>C (n.443+45G>C) c.7984+45G>C (n.7984+45G>C) c.541+45G>C c.7880+45G>C (n.7880+45G>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32362738G= | CA2082832574 | BRCA2 | c.7976+45G= (n.7976+45G=) c.7607+45G= (n.7607+45G=) c.443+45G= (n.443+45G=) c.7984+45G= (n.7984+45G=) c.541+45G= c.7880+45G= (n.7880+45G=) | |
| 13 | g.32362738G>T | CA2798720276 | BRCA2 | c.7976+45G>T (n.7976+45G>T) c.7607+45G>T (n.7607+45G>T) c.443+45G>T (n.443+45G>T) c.7984+45G>T (n.7984+45G>T) c.541+45G>T c.7880+45G>T (n.7880+45G>T) | |
| 13 | g.32362739T>A | CA2727917893 | BRCA2 | c.7976+46T>A (n.7976+46T>A) c.7607+46T>A (n.7607+46T>A) c.443+46T>A (n.443+46T>A) c.7984+46T>A (n.7984+46T>A) c.541+46T>A c.7880+46T>A (n.7880+46T>A) | dbSNP |
| 13 | g.32362740T>A | CA2727917895 | BRCA2 | c.7976+47T>A (n.7976+47T>A) c.7607+47T>A (n.7607+47T>A) c.443+47T>A (n.443+47T>A) c.7984+47T>A (n.7984+47T>A) c.541+47T>A c.7880+47T>A (n.7880+47T>A) | dbSNP |
| 13 | g.32362741A>T | CA2529692393 | BRCA2 | c.7976+48A>T (n.7976+48A>T) c.7607+48A>T (n.7607+48A>T) c.443+48A>T (n.443+48A>T) c.7984+48A>T (n.7984+48A>T) c.541+48A>T c.7880+48A>T (n.7880+48A>T) | |
| 13 | g.32362742A>G | CA2622572919 | BRCA2 | c.7976+49A>G (n.7976+49A>G) c.7607+49A>G (n.7607+49A>G) c.443+49A>G (n.443+49A>G) c.7984+49A>G (n.7984+49A>G) c.541+49A>G c.7880+49A>G (n.7880+49A>G) | gnomAD v4 |
| 13 | g.32362743G>A | CA609091821 | BRCA2 | c.7976+50G>A (n.7976+50G>A) c.7607+50G>A (n.7607+50G>A) c.443+50G>A (n.443+50G>A) c.7984+50G>A (n.7984+50G>A) c.541+50G>A c.7880+50G>A (n.7880+50G>A) | dbSNP gnomAD v2 |
| 13 | g.32362743G>C | CA609091823 | BRCA2 | c.7976+50G>C (n.7976+50G>C) c.7607+50G>C (n.7607+50G>C) c.443+50G>C (n.443+50G>C) c.7984+50G>C (n.7984+50G>C) c.541+50G>C c.7880+50G>C (n.7880+50G>C) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32362743G= | CA2082832584 | BRCA2 | c.7976+50G= (n.7976+50G=) c.7607+50G= (n.7607+50G=) c.443+50G= (n.443+50G=) c.7984+50G= (n.7984+50G=) c.541+50G= c.7880+50G= (n.7880+50G=) | |
| 13 | g.32362743G>T | CA2727870104 | BRCA2 | c.7976+50G>T (n.7976+50G>T) c.7607+50G>T (n.7607+50G>T) c.443+50G>T (n.443+50G>T) c.7984+50G>T (n.7984+50G>T) c.541+50G>T c.7880+50G>T (n.7880+50G>T) | dbSNP |
| 13 | g.32362744G>A | CA2082832615 | BRCA2 | c.7976+51G>A (n.7976+51G>A) c.7607+51G>A (n.7607+51G>A) c.443+51G>A (n.443+51G>A) c.7984+51G>A (n.7984+51G>A) c.541+51G>A c.7880+51G>A (n.7880+51G>A) | dbSNP |
| 13 | g.32362744G>C | CA609091825 | BRCA2 | c.7976+51G>C (n.7976+51G>C) c.7607+51G>C (n.7607+51G>C) c.443+51G>C (n.443+51G>C) c.7984+51G>C (n.7984+51G>C) c.541+51G>C c.7880+51G>C (n.7880+51G>C) | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32362744G= | CA2082832611 | BRCA2 | c.7976+51G= (n.7976+51G=) c.7607+51G= (n.7607+51G=) c.443+51G= (n.443+51G=) c.7984+51G= (n.7984+51G=) c.541+51G= c.7880+51G= (n.7880+51G=) | |
| 13 | g.32362744G>T | CA6941172 | BRCA2 | c.7976+51G>T (n.7976+51G>T) c.7607+51G>T (n.7607+51G>T) c.443+51G>T (n.443+51G>T) c.7984+51G>T (n.7984+51G>T) c.541+51G>T c.7880+51G>T (n.7880+51G>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32362745T>C | CA2526148053 | BRCA2 | c.7976+52T>C (n.7976+52T>C) c.7607+52T>C (n.7607+52T>C) c.443+52T>C (n.443+52T>C) c.7984+52T>C (n.7984+52T>C) c.541+52T>C c.7880+52T>C (n.7880+52T>C) | |
| 13 | g.32362746T>A | CA247475409 | BRCA2 | c.7976+53T>A (n.7976+53T>A) c.7607+53T>A (n.7607+53T>A) c.443+53T>A (n.443+53T>A) c.7984+53T>A (n.7984+53T>A) c.541+53T>A c.7880+53T>A (n.7880+53T>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32362746T= | CA2082832621 | BRCA2 | c.7976+53T= (n.7976+53T=) c.7607+53T= (n.7607+53T=) c.443+53T= (n.443+53T=) c.7984+53T= (n.7984+53T=) c.541+53T= c.7880+53T= (n.7880+53T=) | |
| 13 | g.32362748C>G | CA2727917913 | BRCA2 | c.7976+55C>G (n.7976+55C>G) c.7607+55C>G (n.7607+55C>G) c.443+55C>G (n.443+55C>G) c.7984+55C>G (n.7984+55C>G) c.541+55C>G c.7880+55C>G (n.7880+55C>G) | dbSNP |
| 13 | g.32362748C>T | CA2522096018 | BRCA2 | c.7976+55C>T (n.7976+55C>T) c.7607+55C>T (n.7607+55C>T) c.443+55C>T (n.443+55C>T) c.7984+55C>T (n.7984+55C>T) c.541+55C>T c.7880+55C>T (n.7880+55C>T) | |
| 13 | g.32362750G>A | CA2622572920 | BRCA2 | c.7976+57G>A (n.7976+57G>A) c.7607+57G>A (n.7607+57G>A) c.443+57G>A (n.443+57G>A) c.7984+57G>A (n.7984+57G>A) c.541+57G>A c.7880+57G>A (n.7880+57G>A) | dbSNP gnomAD v4 |
| 13 | g.32362750G>C | CA247475411 | BRCA2 | c.7976+57G>C (n.7976+57G>C) c.7607+57G>C (n.7607+57G>C) c.443+57G>C (n.443+57G>C) c.7984+57G>C (n.7984+57G>C) c.541+57G>C c.7880+57G>C (n.7880+57G>C) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32362750G= | CA2082832624 | BRCA2 | c.7976+57G= (n.7976+57G=) c.7607+57G= (n.7607+57G=) c.443+57G= (n.443+57G=) c.7984+57G= (n.7984+57G=) c.541+57G= c.7880+57G= (n.7880+57G=) | |
| 13 | g.32362751T>A | CA2727917935 | BRCA2 | c.7976+58T>A (n.7976+58T>A) c.7607+58T>A (n.7607+58T>A) c.443+58T>A (n.443+58T>A) c.7984+58T>A (n.7984+58T>A) c.541+58T>A c.7880+58T>A (n.7880+58T>A) | dbSNP |
| 13 | g.32362752G>A | CA2082832637 | BRCA2 | c.7976+59G>A (n.7976+59G>A) c.7607+59G>A (n.7607+59G>A) c.443+59G>A (n.443+59G>A) c.7984+59G>A (n.7984+59G>A) c.541+59G>A c.7880+59G>A (n.7880+59G>A) | dbSNP gnomAD v4 |
| 13 | g.32362752G>C | CA2727912856 | BRCA2 | c.7976+59G>C (n.7976+59G>C) c.7607+59G>C (n.7607+59G>C) c.443+59G>C (n.443+59G>C) c.7984+59G>C (n.7984+59G>C) c.541+59G>C c.7880+59G>C (n.7880+59G>C) | dbSNP |
| 13 | g.32362752G= | CA2082832630 | BRCA2 | c.7976+59G= (n.7976+59G=) c.7607+59G= (n.7607+59G=) c.443+59G= (n.443+59G=) c.7984+59G= (n.7984+59G=) c.541+59G= c.7880+59G= (n.7880+59G=) | |
| 13 | g.32362753T>A | CA2727917939 | BRCA2 | c.7976+60T>A (n.7976+60T>A) c.7607+60T>A (n.7607+60T>A) c.443+60T>A (n.443+60T>A) c.7984+60T>A (n.7984+60T>A) c.541+60T>A c.7880+60T>A (n.7880+60T>A) | dbSNP |
| 13 | g.32362753T>C | CA2508967095 | BRCA2 | c.7976+60T>C (n.7976+60T>C) c.7607+60T>C (n.7607+60T>C) c.443+60T>C (n.443+60T>C) c.7984+60T>C (n.7984+60T>C) c.541+60T>C c.7880+60T>C (n.7880+60T>C) | |
| 13 | g.32362754A>G | CA2727917971 | BRCA2 | c.7976+61A>G (n.7976+61A>G) c.7607+61A>G (n.7607+61A>G) c.443+61A>G (n.443+61A>G) c.7984+61A>G (n.7984+61A>G) c.541+61A>G c.7880+61A>G (n.7880+61A>G) | dbSNP |
| 13 | g.32362754A>T | CA2566381297 | BRCA2 | c.7976+61A>T (n.7976+61A>T) c.7607+61A>T (n.7607+61A>T) c.443+61A>T (n.443+61A>T) c.7984+61A>T (n.7984+61A>T) c.541+61A>T c.7880+61A>T (n.7880+61A>T) | |
| 13 | g.32362755G>C | CA2727917980 | BRCA2 | c.7976+62G>C (n.7976+62G>C) c.7607+62G>C (n.7607+62G>C) c.443+62G>C (n.443+62G>C) c.7984+62G>C (n.7984+62G>C) c.541+62G>C c.7880+62G>C (n.7880+62G>C) | dbSNP |
| 13 | g.32362756T>A | CA2622572921 | BRCA2 | c.7976+63T>A (n.7976+63T>A) c.7607+63T>A (n.7607+63T>A) c.443+63T>A (n.443+63T>A) c.7984+63T>A (n.7984+63T>A) c.541+63T>A c.7880+63T>A (n.7880+63T>A) | dbSNP gnomAD v4 |
| 13 | g.32362757C>A | CA2575388235 | BRCA2 | c.7976+64C>A (n.7976+64C>A) c.7607+64C>A (n.7607+64C>A) c.443+64C>A (n.443+64C>A) c.7984+64C>A (n.7984+64C>A) c.541+64C>A c.7880+64C>A (n.7880+64C>A) | gnomAD v4 |
| 13 | g.32362757C>G | CA2727918002 | BRCA2 | c.7976+64C>G (n.7976+64C>G) c.7607+64C>G (n.7607+64C>G) c.443+64C>G (n.443+64C>G) c.7984+64C>G (n.7984+64C>G) c.541+64C>G c.7880+64C>G (n.7880+64C>G) | dbSNP |
| 13 | g.32362757C>T | CA2727918017 | BRCA2 | c.7976+64C>T (n.7976+64C>T) c.7607+64C>T (n.7607+64C>T) c.443+64C>T (n.443+64C>T) c.7984+64C>T (n.7984+64C>T) c.541+64C>T c.7880+64C>T (n.7880+64C>T) | dbSNP |
| 13 | g.32362757_32362759delinsCTG | CA2082832639 | BRCA2 | c.7976+64_7976+66delinsCTG (n.7976+64_7976+66delinsCTG) c.7607+64_7607+66delinsCTG (n.7607+64_7607+66delinsCTG) c.443+64_443+66delinsCTG (n.443+64_443+66delinsCTG) c.7984+64_7984+66delinsCTG (n.7984+64_7984+66delinsCTG) c.541+64_541+66delinsCTG c.7880+64_7880+66delinsCTG (n.7880+64_7880+66delinsCTG) | |
| 13 | g.32362758T>C | CA2727918025 | BRCA2 | c.7976+65T>C (n.7976+65T>C) c.7607+65T>C (n.7607+65T>C) c.443+65T>C (n.443+65T>C) c.7984+65T>C (n.7984+65T>C) c.541+65T>C c.7880+65T>C (n.7880+65T>C) | dbSNP |
| 13 | g.32362760_32362761del | CA697355381 | BRCA2 | c.7976+67_7976+68del (n.7976+67_7976+68del) c.7607+67_7607+68del (n.7607+67_7607+68del) c.443+67_443+68del (n.443+67_443+68del) c.7984+67_7984+68del (n.7984+67_7984+68del) c.541+67_541+68del c.7880+67_7880+68del (n.7880+67_7880+68del) | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32362759G>A | CA2622572922 | BRCA2 | c.7976+66G>A (n.7976+66G>A) c.7607+66G>A (n.7607+66G>A) c.443+66G>A (n.443+66G>A) c.7984+66G>A (n.7984+66G>A) c.541+66G>A c.7880+66G>A (n.7880+66G>A) | dbSNP gnomAD v4 |
| 13 | g.32362760T>A | CA2727918129 | BRCA2 | c.7976+67T>A (n.7976+67T>A) c.7607+67T>A (n.7607+67T>A) c.443+67T>A (n.443+67T>A) c.7984+67T>A (n.7984+67T>A) c.541+67T>A c.7880+67T>A (n.7880+67T>A) | dbSNP |
| 13 | g.32362761G>A | CA2727918165 | BRCA2 | c.7976+68G>A (n.7976+68G>A) c.7607+68G>A (n.7607+68G>A) c.443+68G>A (n.443+68G>A) c.7984+68G>A (n.7984+68G>A) c.541+68G>A c.7880+68G>A (n.7880+68G>A) | dbSNP |
| 13 | g.32362761G>C | CA2727918166 | BRCA2 | c.7976+68G>C (n.7976+68G>C) c.7607+68G>C (n.7607+68G>C) c.443+68G>C (n.443+68G>C) c.7984+68G>C (n.7984+68G>C) c.541+68G>C c.7880+68G>C (n.7880+68G>C) | dbSNP |
| 13 | g.32362761G>T | CA2622572923 | BRCA2 | c.7976+68G>T (n.7976+68G>T) c.7607+68G>T (n.7607+68G>T) c.443+68G>T (n.443+68G>T) c.7984+68G>T (n.7984+68G>T) c.541+68G>T c.7880+68G>T (n.7880+68G>T) | gnomAD v4 |
| 13 | g.32362763_32362764insATGGAAGTCACAGAC | CA2838665597 | BRCA2 | c.7976+70_7976+71insATGGAAGTCACAGAC (n.7976+70_7976+71insATGGAAGTCACAGAC) c.7607+70_7607+71insATGGAAGTCACAGAC (n.7607+70_7607+71insATGGAAGTCACAGAC) c.443+70_443+71insATGGAAGTCACAGAC (n.443+70_443+71insATGGAAGTCACAGAC) c.7984+70_7984+71insATGGAAGTCACAGAC (n.7984+70_7984+71insATGGAAGTCACAGAC) c.541+70_541+71insATGGAAGTCACAGAC c.7880+70_7880+71insATGGAAGTCACAGAC (n.7880+70_7880+71insATGGAAGTCACAGAC) | |
| 13 | g.32362762A>G | CA2516832644 | BRCA2 | c.7976+69A>G (n.7976+69A>G) c.7607+69A>G (n.7607+69A>G) c.443+69A>G (n.443+69A>G) c.7984+69A>G (n.7984+69A>G) c.541+69A>G c.7880+69A>G (n.7880+69A>G) | |
| 13 | g.32362763C>A | CA2575388236 | BRCA2 | c.7976+70C>A (n.7976+70C>A) c.7607+70C>A (n.7607+70C>A) c.443+70C>A (n.443+70C>A) c.7984+70C>A (n.7984+70C>A) c.541+70C>A c.7880+70C>A (n.7880+70C>A) | |
| 13 | g.32362765T>A | CA2839550517 | BRCA2 | c.7976+72T>A (n.7976+72T>A) c.7607+72T>A (n.7607+72T>A) c.443+72T>A (n.443+72T>A) c.7984+72T>A (n.7984+72T>A) c.541+72T>A c.7880+72T>A (n.7880+72T>A) | |
| 13 | g.32362766C>A | CA2727918171 | BRCA2 | c.7976+73C>A (n.7976+73C>A) c.7607+73C>A (n.7607+73C>A) c.443+73C>A (n.443+73C>A) c.7984+73C>A (n.7984+73C>A) c.541+73C>A c.7880+73C>A (n.7880+73C>A) | dbSNP |
| 13 | g.32362766C>G | CA2727918220 | BRCA2 | c.7976+73C>G (n.7976+73C>G) c.7607+73C>G (n.7607+73C>G) c.443+73C>G (n.443+73C>G) c.7984+73C>G (n.7984+73C>G) c.541+73C>G c.7880+73C>G (n.7880+73C>G) | dbSNP |
| 13 | g.32362766C>T | CA2727918224 | BRCA2 | c.7976+73C>T (n.7976+73C>T) c.7607+73C>T (n.7607+73C>T) c.443+73C>T (n.443+73C>T) c.7984+73C>T (n.7984+73C>T) c.541+73C>T c.7880+73C>T (n.7880+73C>T) | dbSNP |
| 13 | g.32362766_32362767insTA | CA2560090180 | BRCA2 | c.7976+73_7976+74insTA (n.7976+73_7976+74insTA) c.7607+73_7607+74insTA (n.7607+73_7607+74insTA) c.443+73_443+74insTA (n.443+73_443+74insTA) c.7984+73_7984+74insTA (n.7984+73_7984+74insTA) c.541+73_541+74insTA c.7880+73_7880+74insTA (n.7880+73_7880+74insTA) | |
| 13 | g.32362767C>A | CA2575388237 | BRCA2 | c.7976+74C>A (n.7976+74C>A) c.7607+74C>A (n.7607+74C>A) c.443+74C>A (n.443+74C>A) c.7984+74C>A (n.7984+74C>A) c.541+74C>A c.7880+74C>A (n.7880+74C>A) | gnomAD v4 |
| 13 | g.32362767C>G | CA2727918228 | BRCA2 | c.7976+74C>G (n.7976+74C>G) c.7607+74C>G (n.7607+74C>G) c.443+74C>G (n.443+74C>G) c.7984+74C>G (n.7984+74C>G) c.541+74C>G c.7880+74C>G (n.7880+74C>G) | dbSNP |
| 13 | g.32362767C>T | CA2727918265 | BRCA2 | c.7976+74C>T (n.7976+74C>T) c.7607+74C>T (n.7607+74C>T) c.443+74C>T (n.443+74C>T) c.7984+74C>T (n.7984+74C>T) c.541+74C>T c.7880+74C>T (n.7880+74C>T) | dbSNP |
| 13 | g.32362768A= | CA2082832642 | BRCA2 | c.7976+75A= (n.7976+75A=) c.7607+75A= (n.7607+75A=) c.443+75A= (n.443+75A=) c.7984+75A= (n.7984+75A=) c.541+75A= c.7880+75A= (n.7880+75A=) | |
| 13 | g.32362768A>G | CA697355383 | BRCA2 | c.7976+75A>G (n.7976+75A>G) c.7607+75A>G (n.7607+75A>G) c.443+75A>G (n.443+75A>G) c.7984+75A>G (n.7984+75A>G) c.541+75A>G c.7880+75A>G (n.7880+75A>G) | dbSNP gnomAD v4 |
| 13 | g.32362768A>T | CA2622572925 | BRCA2 | c.7976+75A>T (n.7976+75A>T) c.7607+75A>T (n.7607+75A>T) c.443+75A>T (n.443+75A>T) c.7984+75A>T (n.7984+75A>T) c.541+75A>T c.7880+75A>T (n.7880+75A>T) | gnomAD v4 |
| 13 | g.32362769T>C | CA954700385 | BRCA2 | c.7976+76T>C (n.7976+76T>C) c.7607+76T>C (n.7607+76T>C) c.443+76T>C (n.443+76T>C) c.7984+76T>C (n.7984+76T>C) c.541+76T>C c.7880+76T>C (n.7880+76T>C) | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32362769T= | CA2082832647 | BRCA2 | c.7976+76T= (n.7976+76T=) c.7607+76T= (n.7607+76T=) c.443+76T= (n.443+76T=) c.7984+76T= (n.7984+76T=) c.541+76T= c.7880+76T= (n.7880+76T=) | |
| 13 | g.32362770_32362771del | CA2537021834 | BRCA2 | c.7976+77_7976+78del (n.7976+77_7976+78del) c.7607+77_7607+78del (n.7607+77_7607+78del) c.443+77_443+78del (n.443+77_443+78del) c.7984+77_7984+78del (n.7984+77_7984+78del) c.541+77_541+78del c.7880+77_7880+78del (n.7880+77_7880+78del) | |
| 13 | g.32362769_32362772del | CA2798720280 | BRCA2 | c.7976+76_7976+79del (n.7976+76_7976+79del) c.7607+76_7607+79del (n.7607+76_7607+79del) c.443+76_443+79del (n.443+76_443+79del) c.7984+76_7984+79del (n.7984+76_7984+79del) c.541+76_541+79del c.7880+76_7880+79del (n.7880+76_7880+79del) | |
| 13 | g.32362770G>A | CA2082832661 | BRCA2 | c.7976+77G>A (n.7976+77G>A) c.7607+77G>A (n.7607+77G>A) c.443+77G>A (n.443+77G>A) c.7984+77G>A (n.7984+77G>A) c.541+77G>A c.7880+77G>A (n.7880+77G>A) | dbSNP gnomAD v4 |
| 13 | g.32362770G>C | CA2622572926 | BRCA2 | c.7976+77G>C (n.7976+77G>C) c.7607+77G>C (n.7607+77G>C) c.443+77G>C (n.443+77G>C) c.7984+77G>C (n.7984+77G>C) c.541+77G>C c.7880+77G>C (n.7880+77G>C) | dbSNP gnomAD v4 |
| 13 | g.32362770G= | CA2082832656 | BRCA2 | c.7976+77G= (n.7976+77G=) c.7607+77G= (n.7607+77G=) c.443+77G= (n.443+77G=) c.7984+77G= (n.7984+77G=) c.541+77G= c.7880+77G= (n.7880+77G=) | |
| 13 | g.32362770G>T | CA2622572927 | BRCA2 | c.7976+77G>T (n.7976+77G>T) c.7607+77G>T (n.7607+77G>T) c.443+77G>T (n.443+77G>T) c.7984+77G>T (n.7984+77G>T) c.541+77G>T c.7880+77G>T (n.7880+77G>T) | gnomAD v4 |
| 13 | g.32362772C>A | CA2622572928 | BRCA2 | c.7976+79C>A (n.7976+79C>A) c.7607+79C>A (n.7607+79C>A) c.443+79C>A (n.443+79C>A) c.7984+79C>A (n.7984+79C>A) c.541+79C>A c.7880+79C>A (n.7880+79C>A) | gnomAD v4 |
| 13 | g.32362772C= | CA2082832666 | BRCA2 | c.7976+79C= (n.7976+79C=) c.7607+79C= (n.7607+79C=) c.443+79C= (n.443+79C=) c.7984+79C= (n.7984+79C=) c.541+79C= c.7880+79C= (n.7880+79C=) | |
| 13 | g.32362772C>G | CA697355385 | BRCA2 | c.7976+79C>G (n.7976+79C>G) c.7607+79C>G (n.7607+79C>G) c.443+79C>G (n.443+79C>G) c.7984+79C>G (n.7984+79C>G) c.541+79C>G c.7880+79C>G (n.7880+79C>G) | dbSNP |
| 13 | g.32362772C>T | CA247475414 | BRCA2 | c.7976+79C>T (n.7976+79C>T) c.7607+79C>T (n.7607+79C>T) c.443+79C>T (n.443+79C>T) c.7984+79C>T (n.7984+79C>T) c.541+79C>T c.7880+79C>T (n.7880+79C>T) | dbSNP |