| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32338197_32338391del | CA2580618074 | BRCA2 | c.3842_4036del (p.Lys1281_Asp1345del) c.3473_3667del (p.Lys1158_Asp1222del) n.3842_4036del | |
| 13 | g.32338252_32338256del | CA2499222147 | BRCA2 | c.3897_3901del (p.Glu1299AspfsTer7) c.3528_3532del (p.Glu1176AspfsTer7) n.3897_3901del | ClinVar |
| 13 | g.32338254T>A | CA387778787 | BRCA2 | c.3899T>A (p.Met1300Lys) c.3530T>A (p.Met1177Lys) n.3899T>A | dbSNP |
| 13 | g.32338254T>C | CA387778788 | BRCA2 | c.3899T>C (p.Met1300Thr) c.3530T>C (p.Met1177Thr) n.3899T>C | |
| 13 | g.32338254T>G | CA387778789 | BRCA2 | c.3899T>G (p.Met1300Arg) c.3530T>G (p.Met1177Arg) n.3899T>G | |
| 13 | g.32338254T= | CA2082821778 | BRCA2 | c.3899T= (p.Met1300=) c.3530T= (p.Met1177=) n.3899T= | |
| 13 | g.32338254_32338257delinsTGAC | CA2082821776 | BRCA2 | c.3899_3902delinsTGAC (p.Met1300=) c.3530_3533delinsTGAC (p.Met1177=) n.3899_3902delinsTGAC | |
| 13 | g.32338254_32338260delinsTGACTAC | CA2082821774 | BRCA2 | c.3899_3905delinsTGACTAC (p.Met1300=) c.3530_3536delinsTGACTAC (p.Met1177=) n.3899_3905delinsTGACTAC | |
| 13 | g.32338255G>A | CA10579595 | BRCA2 | c.3900G>A (p.Met1300Ile) c.3531G>A (p.Met1177Ile) n.3900G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338255G>C | CA387778790 | BRCA2 | c.3900G>C (p.Met1300Ile) c.3531G>C (p.Met1177Ile) n.3900G>C | dbSNP |
| 13 | g.32338255G= | CA2082821804 | BRCA2 | c.3900G= (p.Met1300=) c.3531G= (p.Met1177=) n.3900G= | |
| 13 | g.32338255G>T | CA387778791 | BRCA2 | c.3900G>T (p.Met1300Ile) c.3531G>T (p.Met1177Ile) n.3900G>T | dbSNP gnomAD v4 |
| 13 | g.32338255_32338257del | CA019096 | BRCA2 | c.3900_3902del (p.Met1300_Thr1301delinsIle) c.3531_3533del (p.Met1177_Thr1178delinsIle) n.3900_3902del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338255_32338257dup | CA2082821800 | BRCA2 | c.3900_3902dup (p.Thr1301_Thr1302insThr) c.3531_3533dup (p.Thr1178_Thr1179insThr) n.3900_3902dup | dbSNP |
| 13 | g.32338255_32338258delinsGACT | CA2082821802 | BRCA2 | c.3900_3903delinsGACT (p.Met1300=) c.3531_3534delinsGACT (p.Met1177=) n.3900_3903delinsGACT | |
| 13 | g.32338255_32338260del | CA019101 | BRCA2 | c.3900_3905del (p.Met1300_Thr1302delinsIle) c.3531_3536del (p.Met1177_Thr1179delinsIle) n.3900_3905del | ClinVar dbSNP |
| 13 | g.32338256A= | CA2082821817 | BRCA2 | c.3901A= (p.Thr1301=) c.3532A= (p.Thr1178=) n.3901A= | |
| 13 | g.32338256A>C | CA387778793 | BRCA2 | c.3901A>C (p.Thr1301Pro) c.3532A>C (p.Thr1178Pro) n.3901A>C | dbSNP |
| 13 | g.32338256A>G | CA387778792 | BRCA2 | c.3901A>G (p.Thr1301Ala) c.3532A>G (p.Thr1178Ala) n.3901A>G | ClinVar dbSNP |
| 13 | g.32338256A>T | CA6940732 | BRCA2 | c.3901A>T (p.Thr1301Ser) c.3532A>T (p.Thr1178Ser) n.3901A>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338259_32338261del | CA019106 | BRCA2 | c.3904_3906del (p.Thr1302del) c.3535_3537del (p.Thr1179del) n.3904_3906del | ClinVar dbSNP |
| 13 | g.32338257C>A | CA387778794 | BRCA2 | c.3902C>A (p.Thr1301Asn) c.3533C>A (p.Thr1178Asn) n.3902C>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338257C= | CA2082821833 | BRCA2 | c.3902C= (p.Thr1301=) c.3533C= (p.Thr1178=) n.3902C= | |
| 13 | g.32338257C>G | CA387778795 | BRCA2 | c.3902C>G (p.Thr1301Ser) c.3533C>G (p.Thr1178Ser) n.3902C>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338257C>T | CA387778796 | BRCA2 | c.3902C>T (p.Thr1301Ile) c.3533C>T (p.Thr1178Ile) n.3902C>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338258T>A | CA483437839 | BRCA2 | c.3903T>A (p.Thr1301=) c.3534T>A (p.Thr1178=) n.3903T>A | dbSNP |
| 13 | g.32338258T>C | CA16606784 | BRCA2 | c.3903T>C (p.Thr1301=) c.3534T>C (p.Thr1178=) n.3903T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338258T>G | CA483437840 | BRCA2 | c.3903T>G (p.Thr1301=) c.3534T>G (p.Thr1178=) n.3903T>G | ClinVar dbSNP |
| 13 | g.32338258T= | CA2082821841 | BRCA2 | c.3903T= (p.Thr1301=) c.3534T= (p.Thr1178=) n.3903T= | |
| 13 | g.32338259A= | CA2082821873 | BRCA2 | c.3904A= (p.Thr1302=) c.3535A= (p.Thr1179=) n.3904A= | |
| 13 | g.32338259A>C | CA387778797 | BRCA2 | c.3904A>C (p.Thr1302Pro) c.3535A>C (p.Thr1179Pro) n.3904A>C | dbSNP |
| 13 | g.32338259A>G | CA019114 | BRCA2 | c.3904A>G (p.Thr1302Ala) c.3535A>G (p.Thr1179Ala) n.3904A>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338259A>T | CA6940733 | BRCA2 | c.3904A>T (p.Thr1302Ser) c.3535A>T (p.Thr1179Ser) n.3904A>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338260C>A | CA019121 | BRCA2 | c.3905C>A (p.Thr1302Asn) c.3536C>A (p.Thr1179Asn) n.3905C>A | ClinVar dbSNP |
| 13 | g.32338260C= | CA2082821902 | BRCA2 | c.3905C= (p.Thr1302=) c.3536C= (p.Thr1179=) n.3905C= | |
| 13 | g.32338260C>G | CA387778798 | BRCA2 | c.3905C>G (p.Thr1302Ser) c.3536C>G (p.Thr1179Ser) n.3905C>G | |
| 13 | g.32338260C>T | CA247506143 | BRCA2 | c.3905C>T (p.Thr1302Ile) c.3536C>T (p.Thr1179Ile) n.3905C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338260_32338261delinsCT | CA2082821886 | BRCA2 | c.3905_3906delinsCT (p.Thr1302=) c.3536_3537delinsCT (p.Thr1179=) n.3905_3906delinsCT | |
| 13 | g.32338261del | CA658798133 | BRCA2 | c.3906del (p.Gly1303AlafsTer?) c.3537del (p.Gly1180AlafsTer?) n.3906del | ClinVar dbSNP |
| 13 | g.32338261T>A | CA483437845 | BRCA2 | c.3906T>A (p.Thr1302=) c.3537T>A (p.Thr1179=) n.3906T>A | gnomAD v4 |
| 13 | g.32338261T>C | CA483437846 | BRCA2 | c.3906T>C (p.Thr1302=) c.3537T>C (p.Thr1179=) n.3906T>C | ClinVar |
| 13 | g.32338261T>G | CA483437848 | BRCA2 | c.3906T>G (p.Thr1302=) c.3537T>G (p.Thr1179=) n.3906T>G | |
| 13 | g.32338262G>A | CA387778799 | BRCA2 | c.3907G>A (p.Gly1303Ser) c.3538G>A (p.Gly1180Ser) n.3907G>A | ClinVar dbSNP |
| 13 | g.32338262G>C | CA387778800 | BRCA2 | c.3907G>C (p.Gly1303Arg) c.3538G>C (p.Gly1180Arg) n.3907G>C | dbSNP |
| 13 | g.32338262G= | CA2082821914 | BRCA2 | c.3907G= (p.Gly1303=) c.3538G= (p.Gly1180=) n.3907G= | |
| 13 | g.32338262G>T | CA387778801 | BRCA2 | c.3907G>T (p.Gly1303Cys) c.3538G>T (p.Gly1180Cys) n.3907G>T | dbSNP gnomAD v4 COSMIC COSMIC |
| 13 | g.32338263G>A | CA019126 | BRCA2 | c.3908G>A (p.Gly1303Asp) c.3539G>A (p.Gly1180Asp) n.3908G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338263G>C | CA387778803 | BRCA2 | c.3908G>C (p.Gly1303Ala) c.3539G>C (p.Gly1180Ala) n.3908G>C | dbSNP |
| 13 | g.32338263G= | CA2082821924 | BRCA2 | c.3908G= (p.Gly1303=) c.3539G= (p.Gly1180=) n.3908G= | |
| 13 | g.32338263G>T | CA387778802 | BRCA2 | c.3908G>T (p.Gly1303Val) c.3539G>T (p.Gly1180Val) n.3908G>T | dbSNP gnomAD v4 |
| 13 | g.32338263_32338264delinsAA | CA2739277537 | BRCA2 | c.3908_3909delinsAA (p.Gly1303Glu) c.3539_3540delinsAA (p.Gly1180Glu) n.3908_3909delinsAA | ClinVar |
| 13 | g.32338264C>A | CA019132 | BRCA2 | c.3909C>A (p.Gly1303=) c.3540C>A (p.Gly1180=) n.3909C>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338264C= | CA2082821931 | BRCA2 | c.3909C= (p.Gly1303=) c.3540C= (p.Gly1180=) n.3909C= | |
| 13 | g.32338264C>G | CA483437854 | BRCA2 | c.3909C>G (p.Gly1303=) c.3540C>G (p.Gly1180=) n.3909C>G | dbSNP |
| 13 | g.32338264C>T | CA483437852 | BRCA2 | c.3909C>T (p.Gly1303=) c.3540C>T (p.Gly1180=) n.3909C>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338265A= | CA2082821948 | BRCA2 | c.3910A= (p.Thr1304=) c.3541A= (p.Thr1181=) n.3910A= | |
| 13 | g.32338265A>C | CA387778804 | BRCA2 | c.3910A>C (p.Thr1304Pro) c.3541A>C (p.Thr1181Pro) n.3910A>C | dbSNP |
| 13 | g.32338265A>G | CA019137 | BRCA2 | c.3910A>G (p.Thr1304Ala) c.3541A>G (p.Thr1181Ala) n.3910A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338265A>T | CA387778805 | BRCA2 | c.3910A>T (p.Thr1304Ser) c.3541A>T (p.Thr1181Ser) n.3910A>T | dbSNP |
| 13 | g.32338265_32338266delinsAC | CA2082821944 | BRCA2 | c.3910_3911delinsAC (p.Thr1304=) c.3541_3542delinsAC (p.Thr1181=) n.3910_3911delinsAC | |
| 13 | g.32338266del | CA019141 | BRCA2 | c.3911del (p.Thr1304IlefsTer?) c.3542del (p.Thr1181IlefsTer?) n.3911del | ClinVar dbSNP |
| 13 | g.32338266C>A | CA387778808 | BRCA2 | c.3911C>A (p.Thr1304Asn) c.3542C>A (p.Thr1181Asn) n.3911C>A | |
| 13 | g.32338266C= | CA2082821960 | BRCA2 | c.3911C= (p.Thr1304=) c.3542C= (p.Thr1181=) n.3911C= | |
| 13 | g.32338266C>G | CA387778806 | BRCA2 | c.3911C>G (p.Thr1304Ser) c.3542C>G (p.Thr1181Ser) n.3911C>G | ClinVar dbSNP |
| 13 | g.32338266C>T | CA387778807 | BRCA2 | c.3911C>T (p.Thr1304Ile) c.3542C>T (p.Thr1181Ile) n.3911C>T | ClinVar dbSNP |
| 13 | g.32338266_32338268delinsCTT | CA2082821963 | BRCA2 | c.3911_3913delinsCTT (p.Thr1304=) c.3542_3544delinsCTT (p.Thr1181=) n.3911_3913delinsCTT | |
| 13 | g.32338267T>A | CA483437862 | BRCA2 | c.3912T>A (p.Thr1304=) c.3543T>A (p.Thr1181=) n.3912T>A | dbSNP |
| 13 | g.32338267T>C | CA483437863 | BRCA2 | c.3912T>C (p.Thr1304=) c.3543T>C (p.Thr1181=) n.3912T>C | dbSNP gnomAD v4 |
| 13 | g.32338267T>G | CA483437864 | BRCA2 | c.3912T>G (p.Thr1304=) c.3543T>G (p.Thr1181=) n.3912T>G | |
| 13 | g.32338270del | CA019164 | BRCA2 | c.3915del (p.Phe1305LeufsTer30) c.3546del (p.Phe1182LeufsTer30) n.3915del | ClinVar dbSNP |
| 13 | g.32338269_32338270del | CA913190942 | BRCA2 | c.3914_3915del (p.Phe1305CysfsTer2) c.3545_3546del (p.Phe1182CysfsTer2) n.3914_3915del | ClinVar dbSNP |
| 13 | g.32338268T>A | CA387778809 | BRCA2 | c.3913T>A (p.Phe1305Ile) c.3544T>A (p.Phe1182Ile) n.3913T>A | dbSNP |
| 13 | g.32338268T>C | CA387778810 | BRCA2 | c.3913T>C (p.Phe1305Leu) c.3544T>C (p.Phe1182Leu) n.3913T>C | dbSNP |
| 13 | g.32338268T>G | CA387778811 | BRCA2 | c.3913T>G (p.Phe1305Val) c.3544T>G (p.Phe1182Val) n.3913T>G | |
| 13 | g.32338269T>A | CA387778812 | BRCA2 | c.3914T>A (p.Phe1305Tyr) c.3545T>A (p.Phe1182Tyr) n.3914T>A | dbSNP |
| 13 | g.32338269T>C | CA019159 | BRCA2 | c.3914T>C (p.Phe1305Ser) c.3545T>C (p.Phe1182Ser) n.3914T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338269T>G | CA387778813 | BRCA2 | c.3914T>G (p.Phe1305Cys) c.3545T>G (p.Phe1182Cys) n.3914T>G | gnomAD v4 |
| 13 | g.32338269T= | CA2082821995 | BRCA2 | c.3914T= (p.Phe1305=) c.3545T= (p.Phe1182=) n.3914T= | |
| 13 | g.32338272_32338274del | CA2580614667 | BRCA2 | c.3917_3919del (p.Val1306del) c.3548_3550del (p.Val1183del) n.3917_3919del | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338270T>A | CA387778814 | BRCA2 | c.3915T>A (p.Phe1305Leu) c.3546T>A (p.Phe1182Leu) n.3915T>A | dbSNP |
| 13 | g.32338270T>C | CA483437866 | BRCA2 | c.3915T>C (p.Phe1305=) c.3546T>C (p.Phe1182=) n.3915T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338270T>G | CA387778815 | BRCA2 | c.3915T>G (p.Phe1305Leu) c.3546T>G (p.Phe1182Leu) n.3915T>G | |
| 13 | g.32338270T= | CA2082822010 | BRCA2 | c.3915T= (p.Phe1305=) c.3546T= (p.Phe1182=) n.3915T= | |
| 13 | g.32338271G>A | CA019173 | BRCA2 | c.3916G>A (p.Val1306Ile) c.3547G>A (p.Val1183Ile) n.3916G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338271G>C | CA387778816 | BRCA2 | c.3916G>C (p.Val1306Leu) c.3547G>C (p.Val1183Leu) n.3916G>C | dbSNP gnomAD v4 |
| 13 | g.32338271G= | CA2082822019 | BRCA2 | c.3916G= (p.Val1306=) c.3547G= (p.Val1183=) n.3916G= | |
| 13 | g.32338271G>T | CA387778817 | BRCA2 | c.3916G>T (p.Val1306Phe) c.3547G>T (p.Val1183Phe) n.3916G>T | |
| 13 | g.32338272T>A | CA387778819 | BRCA2 | c.3917T>A (p.Val1306Asp) c.3548T>A (p.Val1183Asp) n.3917T>A | dbSNP |
| 13 | g.32338272T>C | CA019180 | BRCA2 | c.3917T>C (p.Val1306Ala) c.3548T>C (p.Val1183Ala) n.3917T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338272T>G | CA387778818 | BRCA2 | c.3917T>G (p.Val1306Gly) c.3548T>G (p.Val1183Gly) n.3917T>G | |
| 13 | g.32338272T= | CA2082822028 | BRCA2 | c.3917T= (p.Val1306=) c.3548T= (p.Val1183=) n.3917T= | |
| 13 | g.32338273T>A | CA483437870 | BRCA2 | c.3918T>A (p.Val1306=) c.3549T>A (p.Val1183=) n.3918T>A | dbSNP |
| 13 | g.32338273T>C | CA483437871 | BRCA2 | c.3918T>C (p.Val1306=) c.3549T>C (p.Val1183=) n.3918T>C | dbSNP |
| 13 | g.32338273T>G | CA483437872 | BRCA2 | c.3918T>G (p.Val1306=) c.3549T>G (p.Val1183=) n.3918T>G | |
| 13 | g.32338273_32338274delinsTG | CA2082822032 | BRCA2 | c.3918_3919delinsTG (p.Val1306=) c.3549_3550delinsTG (p.Val1183=) n.3918_3919delinsTG | |
| 13 | g.32338273_32338276delinsTGAA | CA2082822037 | BRCA2 | c.3918_3921delinsTGAA (p.Val1306=) c.3549_3552delinsTGAA (p.Val1183=) n.3918_3921delinsTGAA | |
| 13 | g.32338274del | CA019184 | BRCA2 | c.3919del (p.Glu1307LysfsTer28) c.3550del (p.Glu1184LysfsTer28) n.3919del | ClinVar dbSNP |
| 13 | g.32338274G>A | CA387778820 | BRCA2 | c.3919G>A (p.Glu1307Lys) c.3550G>A (p.Glu1184Lys) n.3919G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338274G>C | CA387778821 | BRCA2 | c.3919G>C (p.Glu1307Gln) c.3550G>C (p.Glu1184Gln) n.3919G>C | dbSNP |
| 13 | g.32338274G>T | CA387778822 | BRCA2 | c.3919G>T (p.Glu1307Ter) c.3550G>T (p.Glu1184Ter) n.3919G>T | dbSNP gnomAD v4 |
| 13 | g.32338274dup | CA2697551723 | BRCA2 | c.3919dup (p.Glu1307GlyfsTer5) c.3550dup (p.Glu1184GlyfsTer5) n.3919dup | ClinVar |
| 13 | g.32338277_32338279del | CA891844452 | BRCA2 | c.3922_3924del (p.Glu1308del) c.3553_3555del (p.Glu1185del) n.3922_3924del | ClinVar dbSNP |
| 13 | g.32338274_32338296delinsGAAGAAATTACTGAAAATTACAA | CA2082822056 | BRCA2 | c.3919_3941delinsGAAGAAATTACTGAAAATTACAA (p.Glu1307=) c.3550_3572delinsGAAGAAATTACTGAAAATTACAA (p.Glu1184=) n.3919_3941delinsGAAGAAATTACTGAAAATTACAA | |
| 13 | g.32338275A= | CA2082822068 | BRCA2 | c.3920A= (p.Glu1307=) c.3551A= (p.Glu1184=) n.3920A= | |
| 13 | g.32338275A>C | CA387778823 | BRCA2 | c.3920A>C (p.Glu1307Ala) c.3551A>C (p.Glu1184Ala) n.3920A>C | |
| 13 | g.32338275A>G | CA387778824 | BRCA2 | c.3920A>G (p.Glu1307Gly) c.3551A>G (p.Glu1184Gly) n.3920A>G | ClinVar dbSNP |
| 13 | g.32338275A>T | CA387778825 | BRCA2 | c.3920A>T (p.Glu1307Val) c.3551A>T (p.Glu1184Val) n.3920A>T | dbSNP |
| 13 | g.32338275_32338296del | CA10589231 | BRCA2 | c.3920_3941del (p.Glu1307GlyfsTer21) c.3551_3572del (p.Glu1184GlyfsTer21) n.3920_3941del | ClinVar dbSNP |
| 13 | g.32338276A>C | CA387778827 | BRCA2 | c.3921A>C (p.Glu1307Asp) c.3552A>C (p.Glu1184Asp) n.3921A>C | |
| 13 | g.32338276A>G | CA483437881 | BRCA2 | c.3921A>G (p.Glu1307=) c.3552A>G (p.Glu1184=) n.3921A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338276A>T | CA387778828 | BRCA2 | c.3921A>T (p.Glu1307Asp) c.3552A>T (p.Glu1184Asp) n.3921A>T | |
| 13 | g.32338277G>A | CA387778829 | BRCA2 | c.3922G>A (p.Glu1308Lys) c.3553G>A (p.Glu1185Lys) n.3922G>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338277G>C | CA387778830 | BRCA2 | c.3922G>C (p.Glu1308Gln) c.3553G>C (p.Glu1185Gln) n.3922G>C | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
| 13 | g.32338277G= | CA2082822081 | BRCA2 | c.3922G= (p.Glu1308=) c.3553G= (p.Glu1185=) n.3922G= | |
| 13 | g.32338277G>T | CA019195 | BRCA2 | c.3922G>T (p.Glu1308Ter) c.3553G>T (p.Glu1185Ter) n.3922G>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338278A>C | CA387778833 | BRCA2 | c.3923A>C (p.Glu1308Ala) c.3554A>C (p.Glu1185Ala) n.3923A>C | ClinVar dbSNP |
| 13 | g.32338278A>G | CA387778832 | BRCA2 | c.3923A>G (p.Glu1308Gly) c.3554A>G (p.Glu1185Gly) n.3923A>G | |
| 13 | g.32338278A>T | CA387778831 | BRCA2 | c.3923A>T (p.Glu1308Val) c.3554A>T (p.Glu1185Val) n.3923A>T | |
| 13 | g.32338280del | CA2739277538 | BRCA2 | c.3925del (p.Ile1309LeufsTer26) c.3556del (p.Ile1186LeufsTer26) n.3925del | ClinVar |
| 13 | g.32338279A>C | CA387778834 | BRCA2 | c.3924A>C (p.Glu1308Asp) c.3555A>C (p.Glu1185Asp) n.3924A>C | ClinVar |
| 13 | g.32338279A>G | CA483437884 | BRCA2 | c.3924A>G (p.Glu1308=) c.3555A>G (p.Glu1185=) n.3924A>G | dbSNP |
| 13 | g.32338279A>T | CA387778835 | BRCA2 | c.3924A>T (p.Glu1308Asp) c.3555A>T (p.Glu1185Asp) n.3924A>T | |
| 13 | g.32338280A= | CA2082822099 | BRCA2 | c.3925A= (p.Ile1309=) c.3556A= (p.Ile1186=) n.3925A= | |
| 13 | g.32338280A>C | CA387778836 | BRCA2 | c.3925A>C (p.Ile1309Leu) c.3556A>C (p.Ile1186Leu) n.3925A>C | |
| 13 | g.32338280A>G | CA019203 | BRCA2 | c.3925A>G (p.Ile1309Val) c.3556A>G (p.Ile1186Val) n.3925A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338280A>T | CA387778837 | BRCA2 | c.3925A>T (p.Ile1309Phe) c.3556A>T (p.Ile1186Phe) n.3925A>T | |
| 13 | g.32338281T>A | CA387778838 | BRCA2 | c.3926T>A (p.Ile1309Asn) c.3557T>A (p.Ile1186Asn) n.3926T>A | gnomAD v4 |
| 13 | g.32338281T>C | CA387778839 | BRCA2 | c.3926T>C (p.Ile1309Thr) c.3557T>C (p.Ile1186Thr) n.3926T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338281T>G | CA387778840 | BRCA2 | c.3926T>G (p.Ile1309Ser) c.3557T>G (p.Ile1186Ser) n.3926T>G | ClinVar dbSNP |
| 13 | g.32338281T= | CA2082822116 | BRCA2 | c.3926T= (p.Ile1309=) c.3557T= (p.Ile1186=) n.3926T= | |
| 13 | g.32338281_32338282del | CA2825002133 | BRCA2 | c.3926_3927del (p.Ile1309AsnfsTer2) c.3557_3558del (p.Ile1186AsnfsTer2) n.3926_3927del | ClinVar |
| 13 | g.32338282T>A | CA483437890 | BRCA2 | c.3927T>A (p.Ile1309=) c.3558T>A (p.Ile1186=) n.3927T>A | dbSNP |
| 13 | g.32338282T>C | CA10583096 | BRCA2 | c.3927T>C (p.Ile1309=) c.3558T>C (p.Ile1186=) n.3927T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338282T>G | CA387778841 | BRCA2 | c.3927T>G (p.Ile1309Met) c.3558T>G (p.Ile1186Met) n.3927T>G | |
| 13 | g.32338282T= | CA2082822145 | BRCA2 | c.3927T= (p.Ile1309=) c.3558T= (p.Ile1186=) n.3927T= | |
| 13 | g.32338292_32338312del | CA2575387802 | BRCA2 | c.3937_3957del (p.Tyr1313_Asn1319del) c.3568_3588del (p.Tyr1190_Asn1196del) n.3937_3957del | |
| 13 | g.32338283A= | CA2082822155 | BRCA2 | c.3928A= (p.Thr1310=) c.3559A= (p.Thr1187=) n.3928A= | |
| 13 | g.32338283A>C | CA387778842 | BRCA2 | c.3928A>C (p.Thr1310Pro) c.3559A>C (p.Thr1187Pro) n.3928A>C | dbSNP |
| 13 | g.32338283A>G | CA387778843 | BRCA2 | c.3928A>G (p.Thr1310Ala) c.3559A>G (p.Thr1187Ala) n.3928A>G | ClinVar |
| 13 | g.32338283A>T | CA387778844 | BRCA2 | c.3928A>T (p.Thr1310Ser) c.3559A>T (p.Thr1187Ser) n.3928A>T | ClinVar dbSNP |
| 13 | g.32338283dup | CA916080547 | BRCA2 | c.3928dup (p.Thr1310AsnfsTer2) c.3559dup (p.Thr1187AsnfsTer2) n.3928dup | ClinVar dbSNP |
| 13 | g.32338283_32338284delinsAC | CA2082822157 | BRCA2 | c.3928_3929delinsAC (p.Thr1310=) c.3559_3560delinsAC (p.Thr1187=) n.3928_3929delinsAC | |
| 13 | g.32338284del | CA019210 | BRCA2 | c.3929del (p.Thr1310MetfsTer25) c.3560del (p.Thr1187MetfsTer25) n.3929del | ClinVar dbSNP |
| 13 | g.32338284C>A | CA387778845 | BRCA2 | c.3929C>A (p.Thr1310Asn) c.3560C>A (p.Thr1187Asn) n.3929C>A | dbSNP gnomAD v4 |
| 13 | g.32338284C= | CA2082822188 | BRCA2 | c.3929C= (p.Thr1310=) c.3560C= (p.Thr1187=) n.3929C= | |
| 13 | g.32338284C>G | CA387778846 | BRCA2 | c.3929C>G (p.Thr1310Ser) c.3560C>G (p.Thr1187Ser) n.3929C>G | dbSNP |
| 13 | g.32338284C>T | CA019205 | BRCA2 | c.3929C>T (p.Thr1310Ile) c.3560C>T (p.Thr1187Ile) n.3929C>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338285T>A | CA483437896 | BRCA2 | c.3930T>A (p.Thr1310=) c.3561T>A (p.Thr1187=) n.3930T>A | dbSNP |
| 13 | g.32338285T>C | CA019217 | BRCA2 | c.3930T>C (p.Thr1310=) c.3561T>C (p.Thr1187=) n.3930T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338285T>G | CA483437898 | BRCA2 | c.3930T>G (p.Thr1310=) c.3561T>G (p.Thr1187=) n.3930T>G | |
| 13 | g.32338285T= | CA2082822200 | BRCA2 | c.3930T= (p.Thr1310=) c.3561T= (p.Thr1187=) n.3930T= | |
| 13 | g.32338285_32338296delinsTGAAAATTACAA | CA2082822209 | BRCA2 | c.3930_3941delinsTGAAAATTACAA (p.Thr1310=) c.3561_3572delinsTGAAAATTACAA (p.Thr1187=) n.3930_3941delinsTGAAAATTACAA | |
| 13 | g.32338286G>A | CA387778847 | BRCA2 | c.3931G>A (p.Glu1311Lys) c.3562G>A (p.Glu1188Lys) n.3931G>A | dbSNP gnomAD v4 |
| 13 | g.32338286G>C | CA387778849 | BRCA2 | c.3931G>C (p.Glu1311Gln) c.3562G>C (p.Glu1188Gln) n.3931G>C | dbSNP |
| 13 | g.32338286G= | CA2082822234 | BRCA2 | c.3931G= (p.Glu1311=) c.3562G= (p.Glu1188=) n.3931G= | |
| 13 | g.32338286G>T | CA387778848 | BRCA2 | c.3931G>T (p.Glu1311Ter) c.3562G>T (p.Glu1188Ter) n.3931G>T | |
| 13 | g.32338288_32338298del | CA658798134 | BRCA2 | c.3933_3943del (p.Asn1312LysfsTer3) c.3564_3574del (p.Asn1189LysfsTer3) n.3933_3943del | ClinVar dbSNP |
| 13 | g.32338287A= | CA2082822241 | BRCA2 | c.3932A= (p.Glu1311=) c.3563A= (p.Glu1188=) n.3932A= | |
| 13 | g.32338287A>C | CA387778850 | BRCA2 | c.3932A>C (p.Glu1311Ala) c.3563A>C (p.Glu1188Ala) n.3932A>C | ClinVar dbSNP |
| 13 | g.32338287A>G | CA387778852 | BRCA2 | c.3932A>G (p.Glu1311Gly) c.3563A>G (p.Glu1188Gly) n.3932A>G | ClinVar dbSNP |
| 13 | g.32338287A>T | CA387778851 | BRCA2 | c.3932A>T (p.Glu1311Val) c.3563A>T (p.Glu1188Val) n.3932A>T | dbSNP |
| 13 | g.32338290dup | CA913190943 | BRCA2 | c.3935dup (p.Asn1312LysfsTer7) c.3566dup (p.Asn1189LysfsTer7) n.3935dup | ClinVar dbSNP |
| 13 | g.32338290del | CA2580087230 | BRCA2 | c.3935del (p.Asn1312IlefsTer23) c.3566del (p.Asn1189IlefsTer23) n.3935del | ClinVar |
| 13 | g.32338289_32338290del | CA2580614670 | BRCA2 | c.3934_3935del (p.Asn1312LeufsTer6) c.3565_3566del (p.Asn1189LeufsTer6) n.3934_3935del | ClinVar |
| 13 | g.32338288A>C | CA387778853 | BRCA2 | c.3933A>C (p.Glu1311Asp) c.3564A>C (p.Glu1188Asp) n.3933A>C | |
| 13 | g.32338288A>G | CA483437903 | BRCA2 | c.3933A>G (p.Glu1311=) c.3564A>G (p.Glu1188=) n.3933A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338288A>T | CA387778854 | BRCA2 | c.3933A>T (p.Glu1311Asp) c.3564A>T (p.Glu1188Asp) n.3933A>T | |
| 13 | g.32338288_32338307delinsAAATTACAAGAGAAATACTG | CA2082822250 | BRCA2 | c.3933_3952delinsAAATTACAAGAGAAATACTG (p.Glu1311=) c.3564_3583delinsAAATTACAAGAGAAATACTG (p.Glu1188=) n.3933_3952delinsAAATTACAAGAGAAATACTG | |
| 13 | g.32338289A>C | CA387778855 | BRCA2 | c.3934A>C (p.Asn1312His) c.3565A>C (p.Asn1189His) n.3934A>C | |
| 13 | g.32338289A>G | CA387778856 | BRCA2 | c.3934A>G (p.Asn1312Asp) c.3565A>G (p.Asn1189Asp) n.3934A>G | gnomAD v4 |
| 13 | g.32338289A>T | CA387778857 | BRCA2 | c.3934A>T (p.Asn1312Tyr) c.3565A>T (p.Asn1189Tyr) n.3934A>T | dbSNP |
| 13 | g.32338291_32338309del | CA019222 | BRCA2 | c.3936_3954del (p.Asn1312LysfsTer17) c.3567_3585del (p.Asn1189LysfsTer17) n.3936_3954del | ClinVar dbSNP |
| 13 | g.32338290A>C | CA387778858 | BRCA2 | c.3935A>C (p.Asn1312Thr) c.3566A>C (p.Asn1189Thr) n.3935A>C | |
| 13 | g.32338290A>G | CA387778859 | BRCA2 | c.3935A>G (p.Asn1312Ser) c.3566A>G (p.Asn1189Ser) n.3935A>G | |
| 13 | g.32338290A>T | CA387778860 | BRCA2 | c.3935A>T (p.Asn1312Ile) c.3566A>T (p.Asn1189Ile) n.3935A>T | |
| 13 | g.32338290_32338291delinsAT | CA2082822257 | BRCA2 | c.3935_3936delinsAT (p.Asn1312=) c.3566_3567delinsAT (p.Asn1189=) n.3935_3936delinsAT | |
| 13 | g.32338291T>A | CA387778861 | BRCA2 | c.3936T>A (p.Asn1312Lys) c.3567T>A (p.Asn1189Lys) n.3936T>A | dbSNP |
| 13 | g.32338291T>C | CA10579596 | BRCA2 | c.3936T>C (p.Asn1312=) c.3567T>C (p.Asn1189=) n.3936T>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338291T>G | CA387778862 | BRCA2 | c.3936T>G (p.Asn1312Lys) c.3567T>G (p.Asn1189Lys) n.3936T>G | ClinVar dbSNP |
| 13 | g.32338291T= | CA2082822271 | BRCA2 | c.3936T= (p.Asn1312=) c.3567T= (p.Asn1189=) n.3936T= | |
| 13 | g.32338292del | CA913190944 | BRCA2 | c.3937del (p.Tyr1313ThrfsTer22) c.3568del (p.Tyr1190ThrfsTer22) n.3937del | ClinVar dbSNP |
| 13 | g.32338292T>A | CA387778863 | BRCA2 | c.3937T>A (p.Tyr1313Asn) c.3568T>A (p.Tyr1190Asn) n.3937T>A | dbSNP |
| 13 | g.32338292T>C | CA387778865 | BRCA2 | c.3937T>C (p.Tyr1313His) c.3568T>C (p.Tyr1190His) n.3937T>C | |
| 13 | g.32338292T>G | CA387778864 | BRCA2 | c.3937T>G (p.Tyr1313Asp) c.3568T>G (p.Tyr1190Asp) n.3937T>G | ClinVar |
| 13 | g.32338293A= | CA2082822283 | BRCA2 | c.3938A= (p.Tyr1313=) c.3569A= (p.Tyr1190=) n.3938A= | |
| 13 | g.32338293A>C | CA019228 | BRCA2 | c.3938A>C (p.Tyr1313Ser) c.3569A>C (p.Tyr1190Ser) n.3938A>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338293A>G | CA019236 | BRCA2 | c.3938A>G (p.Tyr1313Cys) c.3569A>G (p.Tyr1190Cys) n.3938A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338293A>T | CA387778866 | BRCA2 | c.3938A>T (p.Tyr1313Phe) c.3569A>T (p.Tyr1190Phe) n.3938A>T | dbSNP |
| 13 | g.32338293dup | CA2573149353 | BRCA2 | c.3938dup (p.Tyr1313Ter) c.3569dup (p.Tyr1190Ter) n.3938dup | ClinVar dbSNP |
| 13 | g.32338293_32338294delinsAC | CA2082822284 | BRCA2 | c.3938_3939delinsAC (p.Tyr1313=) c.3569_3570delinsAC (p.Tyr1190=) n.3938_3939delinsAC | |
| 13 | g.32338294_32338298del | CA2573053808 | BRCA2 | c.3939_3943del (p.Tyr1313Ter) c.3570_3574del (p.Tyr1190Ter) n.3939_3943del | ClinVar dbSNP |
| 13 | g.32338294del | CA019249 | BRCA2 | c.3939del (p.Tyr1313Ter) c.3570del (p.Tyr1190Ter) n.3939del | ClinVar dbSNP |
| 13 | g.32338294C>A | CA019241 | BRCA2 | c.3939C>A (p.Tyr1313Ter) c.3570C>A (p.Tyr1190Ter) n.3939C>A | ClinVar dbSNP |
| 13 | g.32338294C= | CA2082822300 | BRCA2 | c.3939C= (p.Tyr1313=) c.3570C= (p.Tyr1190=) n.3939C= | |
| 13 | g.32338294C>G | CA019246 | BRCA2 | c.3939C>G (p.Tyr1313Ter) c.3570C>G (p.Tyr1190Ter) n.3939C>G | ClinVar dbSNP |
| 13 | g.32338294C>T | CA483437911 | BRCA2 | c.3939C>T (p.Tyr1313=) c.3570C>T (p.Tyr1190=) n.3939C>T | dbSNP gnomAD v4 |
| 13 | g.32338294_32338296delinsCAA | CA2082822307 | BRCA2 | c.3939_3941delinsCAA (p.Tyr1313=) c.3570_3572delinsCAA (p.Tyr1190=) n.3939_3941delinsCAA | |
| 13 | g.32338295A>C | CA387778867 | BRCA2 | c.3940A>C (p.Lys1314Gln) c.3571A>C (p.Lys1191Gln) n.3940A>C | gnomAD v4 |
| 13 | g.32338295A>G | CA387778868 | BRCA2 | c.3940A>G (p.Lys1314Glu) c.3571A>G (p.Lys1191Glu) n.3940A>G | dbSNP |
| 13 | g.32338295A>T | CA387778869 | BRCA2 | c.3940A>T (p.Lys1314Ter) c.3571A>T (p.Lys1191Ter) n.3940A>T | ClinVar |
| 13 | g.32338295_32338296del | CA658683802 | BRCA2 | c.3940_3941del (p.Lys1314GlufsTer4) c.3571_3572del (p.Lys1191GlufsTer4) n.3940_3941del | ClinVar dbSNP |
| 13 | g.32338296A= | CA2082822326 | BRCA2 | c.3941A= (p.Lys1314=) c.3572A= (p.Lys1191=) n.3941A= | |
| 13 | g.32338296A>C | CA387778871 | BRCA2 | c.3941A>C (p.Lys1314Thr) c.3572A>C (p.Lys1191Thr) n.3941A>C | |
| 13 | g.32338296A>G | CA387778872 | BRCA2 | c.3941A>G (p.Lys1314Arg) c.3572A>G (p.Lys1191Arg) n.3941A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338296A>T | CA387778870 | BRCA2 | c.3941A>T (p.Lys1314Met) c.3572A>T (p.Lys1191Met) n.3941A>T | dbSNP |
| 13 | g.32338297G>A | CA16607463 | BRCA2 | c.3942G>A (p.Lys1314=) c.3573G>A (p.Lys1191=) n.3942G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338297G>C | CA247506205 | BRCA2 | c.3942G>C (p.Lys1314Asn) c.3573G>C (p.Lys1191Asn) n.3942G>C | dbSNP |
| 13 | g.32338297G= | CA2082822342 | BRCA2 | c.3942G= (p.Lys1314=) c.3573G= (p.Lys1191=) n.3942G= | |
| 13 | g.32338297G>T | CA387778873 | BRCA2 | c.3942G>T (p.Lys1314Asn) c.3573G>T (p.Lys1191Asn) n.3942G>T | gnomAD v4 |
| 13 | g.32338298A>C | CA483437919 | BRCA2 | c.3943A>C (p.Arg1315=) c.3574A>C (p.Arg1192=) n.3943A>C | |
| 13 | g.32338298A>G | CA387778874 | BRCA2 | c.3943A>G (p.Arg1315Gly) c.3574A>G (p.Arg1192Gly) n.3943A>G | |
| 13 | g.32338298A>T | CA387778875 | BRCA2 | c.3943A>T (p.Arg1315Ter) c.3574A>T (p.Arg1192Ter) n.3943A>T | |
| 13 | g.32338299G>A | CA019254 | BRCA2 | c.3944G>A (p.Arg1315Lys) c.3575G>A (p.Arg1192Lys) n.3944G>A | ClinVar dbSNP |
| 13 | g.32338299G>C | CA387778876 | BRCA2 | c.3944G>C (p.Arg1315Thr) c.3575G>C (p.Arg1192Thr) n.3944G>C | ClinVar dbSNP |
| 13 | g.32338299G= | CA2082822345 | BRCA2 | c.3944G= (p.Arg1315=) c.3575G= (p.Arg1192=) n.3944G= | |
| 13 | g.32338299G>T | CA387778877 | BRCA2 | c.3944G>T (p.Arg1315Ile) c.3575G>T (p.Arg1192Ile) n.3944G>T | gnomAD v4 |
| 13 | g.32338300A>C | CA387778878 | BRCA2 | c.3945A>C (p.Arg1315Ser) c.3576A>C (p.Arg1192Ser) n.3945A>C | |
| 13 | g.32338300A>G | CA483437921 | BRCA2 | c.3945A>G (p.Arg1315=) c.3576A>G (p.Arg1192=) n.3945A>G | gnomAD v4 |
| 13 | g.32338300A>T | CA387778879 | BRCA2 | c.3945A>T (p.Arg1315Ser) c.3576A>T (p.Arg1192Ser) n.3945A>T | ClinVar dbSNP |
| 13 | g.32338301_32338302del | CA2580087231 | BRCA2 | c.3946_3947del (p.Asn1316TyrfsTer2) c.3577_3578del (p.Asn1193TyrfsTer2) n.3946_3947del | ClinVar |
| 13 | g.32338301A>C | CA387778880 | BRCA2 | c.3946A>C (p.Asn1316His) c.3577A>C (p.Asn1193His) n.3946A>C | |
| 13 | g.32338301A>G | CA387778881 | BRCA2 | c.3946A>G (p.Asn1316Asp) c.3577A>G (p.Asn1193Asp) n.3946A>G | gnomAD v4 |
| 13 | g.32338301A>T | CA387778882 | BRCA2 | c.3946A>T (p.Asn1316Tyr) c.3577A>T (p.Asn1193Tyr) n.3946A>T | |
| 13 | g.32338302A= | CA2082822351 | BRCA2 | c.3947A= (p.Asn1316=) c.3578A= (p.Asn1193=) n.3947A= | |
| 13 | g.32338302A>C | CA387778885 | BRCA2 | c.3947A>C (p.Asn1316Thr) c.3578A>C (p.Asn1193Thr) n.3947A>C | |
| 13 | g.32338302A>G | CA387778883 | BRCA2 | c.3947A>G (p.Asn1316Ser) c.3578A>G (p.Asn1193Ser) n.3947A>G | ClinVar dbSNP |
| 13 | g.32338302A>T | CA387778884 | BRCA2 | c.3947A>T (p.Asn1316Ile) c.3578A>T (p.Asn1193Ile) n.3947A>T | dbSNP |
| 13 | g.32338303T>A | CA387778886 | BRCA2 | c.3948T>A (p.Asn1316Lys) c.3579T>A (p.Asn1193Lys) n.3948T>A | dbSNP |
| 13 | g.32338303T>C | CA483437928 | BRCA2 | c.3948T>C (p.Asn1316=) c.3579T>C (p.Asn1193=) n.3948T>C | ClinVar |
| 13 | g.32338303T>G | CA387778887 | BRCA2 | c.3948T>G (p.Asn1316Lys) c.3579T>G (p.Asn1193Lys) n.3948T>G | dbSNP |
| 13 | g.32338304A= | CA2082822360 | BRCA2 | c.3949A= (p.Thr1317=) c.3580A= (p.Thr1194=) n.3949A= | |
| 13 | g.32338304A>C | CA387778888 | BRCA2 | c.3949A>C (p.Thr1317Pro) c.3580A>C (p.Thr1194Pro) n.3949A>C | dbSNP |
| 13 | g.32338304A>G | CA387778889 | BRCA2 | c.3949A>G (p.Thr1317Ala) c.3580A>G (p.Thr1194Ala) n.3949A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338304A>T | CA019259 | BRCA2 | c.3949A>T (p.Thr1317Ser) c.3580A>T (p.Thr1194Ser) n.3949A>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338305del | CA2499222148 | BRCA2 | c.3950del (p.Thr1317MetfsTer18) c.3581del (p.Thr1194MetfsTer18) n.3950del | |
| 13 | g.32338305C>A | CA387778890 | BRCA2 | c.3950C>A (p.Thr1317Asn) c.3581C>A (p.Thr1194Asn) n.3950C>A | dbSNP gnomAD v4 |
| 13 | g.32338305C= | CA2082822380 | BRCA2 | c.3950C= (p.Thr1317=) c.3581C= (p.Thr1194=) n.3950C= | |
| 13 | g.32338305C>G | CA387778891 | BRCA2 | c.3950C>G (p.Thr1317Ser) c.3581C>G (p.Thr1194Ser) n.3950C>G | ClinVar dbSNP |
| 13 | g.32338305C>T | CA387778892 | BRCA2 | c.3950C>T (p.Thr1317Ile) c.3581C>T (p.Thr1194Ile) n.3950C>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338306T>A | CA483437931 | BRCA2 | c.3951T>A (p.Thr1317=) c.3582T>A (p.Thr1194=) n.3951T>A | |
| 13 | g.32338306T>C | CA6940734 | BRCA2 | c.3951T>C (p.Thr1317=) c.3582T>C (p.Thr1194=) n.3951T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338306T>G | CA483437932 | BRCA2 | c.3951T>G (p.Thr1317=) c.3582T>G (p.Thr1194=) n.3951T>G | |
| 13 | g.32338306T= | CA2082822388 | BRCA2 | c.3951T= (p.Thr1317=) c.3582T= (p.Thr1194=) n.3951T= | |
| 13 | g.32338307G>A | CA387778893 | BRCA2 | c.3952G>A (p.Glu1318Lys) c.3583G>A (p.Glu1195Lys) n.3952G>A | ClinVar gnomAD v4 |
| 13 | g.32338307G>C | CA387778894 | BRCA2 | c.3952G>C (p.Glu1318Gln) c.3583G>C (p.Glu1195Gln) n.3952G>C | dbSNP |
| 13 | g.32338307G>T | CA387778895 | BRCA2 | c.3952G>T (p.Glu1318Ter) c.3583G>T (p.Glu1195Ter) n.3952G>T | |
| 13 | g.32338308A>C | CA387778898 | BRCA2 | c.3953A>C (p.Glu1318Ala) c.3584A>C (p.Glu1195Ala) n.3953A>C | |
| 13 | g.32338308A>G | CA387778897 | BRCA2 | c.3953A>G (p.Glu1318Gly) c.3584A>G (p.Glu1195Gly) n.3953A>G | gnomAD v4 |
| 13 | g.32338308A>T | CA387778896 | BRCA2 | c.3953A>T (p.Glu1318Val) c.3584A>T (p.Glu1195Val) n.3953A>T | dbSNP |
| 13 | g.32338311del | CA2580087232 | BRCA2 | c.3956del (p.Asn1319MetfsTer16) c.3587del (p.Asn1196MetfsTer16) n.3956del | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338309A>C | CA387778899 | BRCA2 | c.3954A>C (p.Glu1318Asp) c.3585A>C (p.Glu1195Asp) n.3954A>C | |
| 13 | g.32338309A>G | CA483437939 | BRCA2 | c.3954A>G (p.Glu1318=) c.3585A>G (p.Glu1195=) n.3954A>G | dbSNP |
| 13 | g.32338309A>T | CA387778900 | BRCA2 | c.3954A>T (p.Glu1318Asp) c.3585A>T (p.Glu1195Asp) n.3954A>T | dbSNP |
| 13 | g.32338309_32338313delinsAAATG | CA2082822395 | BRCA2 | c.3954_3958delinsAAATG (p.Glu1318=) c.3585_3589delinsAAATG (p.Glu1195=) n.3954_3958delinsAAATG | |
| 13 | g.32338310A>C | CA387778901 | BRCA2 | c.3955A>C (p.Asn1319His) c.3586A>C (p.Asn1196His) n.3955A>C | |
| 13 | g.32338310A>G | CA387778902 | BRCA2 | c.3955A>G (p.Asn1319Asp) c.3586A>G (p.Asn1196Asp) n.3955A>G | dbSNP |
| 13 | g.32338310A>T | CA387778903 | BRCA2 | c.3955A>T (p.Asn1319Tyr) c.3586A>T (p.Asn1196Tyr) n.3955A>T | dbSNP |
| 13 | g.32338312_32338315del | CA019261 | BRCA2 | c.3957_3960del (p.Asn1319LysfsTer15) c.3588_3591del (p.Asn1196LysfsTer15) n.3957_3960del | ClinVar dbSNP |
| 13 | g.32338311A>C | CA387778904 | BRCA2 | c.3956A>C (p.Asn1319Thr) c.3587A>C (p.Asn1196Thr) n.3956A>C | |
| 13 | g.32338311A>G | CA387778905 | BRCA2 | c.3956A>G (p.Asn1319Ser) c.3587A>G (p.Asn1196Ser) n.3956A>G | dbSNP |
| 13 | g.32338311A>T | CA387778906 | BRCA2 | c.3956A>T (p.Asn1319Ile) c.3587A>T (p.Asn1196Ile) n.3956A>T | |
| 13 | g.32338311_32338313delinsATG | CA2082822406 | BRCA2 | c.3956_3958delinsATG (p.Asn1319=) c.3587_3589delinsATG (p.Asn1196=) n.3956_3958delinsATG | |
| 13 | g.32338313_32338318del | CA2580087233 | BRCA2 | c.3958_3963del (p.Glu1320_Asp1321del) c.3589_3594del (p.Glu1197_Asp1198del) n.3958_3963del | ClinVar dbSNP |
| 13 | g.32338312T>A | CA387778907 | BRCA2 | c.3957T>A (p.Asn1319Lys) c.3588T>A (p.Asn1196Lys) n.3957T>A | dbSNP |
| 13 | g.32338312T>C | CA483437945 | BRCA2 | c.3957T>C (p.Asn1319=) c.3588T>C (p.Asn1196=) n.3957T>C | ClinVar dbSNP |
| 13 | g.32338312T>G | CA387778908 | BRCA2 | c.3957T>G (p.Asn1319Lys) c.3588T>G (p.Asn1196Lys) n.3957T>G | dbSNP |
| 13 | g.32338312T= | CA2082822421 | BRCA2 | c.3957T= (p.Asn1319=) c.3588T= (p.Asn1196=) n.3957T= | |
| 13 | g.32338312_32338313del | CA10589232 | BRCA2 | c.3957_3958del (p.Asn1319LysfsTer3) c.3588_3589del (p.Asn1196LysfsTer3) n.3957_3958del | ClinVar dbSNP |
| 13 | g.32338313G>A | CA10583097 | BRCA2 | c.3958G>A (p.Glu1320Lys) c.3589G>A (p.Glu1197Lys) n.3958G>A | ClinVar dbSNP |
| 13 | g.32338313G>C | CA387778909 | BRCA2 | c.3958G>C (p.Glu1320Gln) c.3589G>C (p.Glu1197Gln) n.3958G>C | dbSNP |
| 13 | g.32338313G= | CA2082822445 | BRCA2 | c.3958G= (p.Glu1320=) c.3589G= (p.Glu1197=) n.3958G= | |
| 13 | g.32338313G>T | CA019267 | BRCA2 | c.3958G>T (p.Glu1320Ter) c.3589G>T (p.Glu1197Ter) n.3958G>T | ClinVar dbSNP |
| 13 | g.32338314A>C | CA387778910 | BRCA2 | c.3959A>C (p.Glu1320Ala) c.3590A>C (p.Glu1197Ala) n.3959A>C | ClinVar |
| 13 | g.32338314A>G | CA387778912 | BRCA2 | c.3959A>G (p.Glu1320Gly) c.3590A>G (p.Glu1197Gly) n.3959A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338314A>T | CA387778911 | BRCA2 | c.3959A>T (p.Glu1320Val) c.3590A>T (p.Glu1197Val) n.3959A>T | dbSNP |
| 13 | g.32338315A= | CA2082822458 | BRCA2 | c.3960A= (p.Glu1320=) c.3591A= (p.Glu1197=) n.3960A= | |
| 13 | g.32338315A>C | CA387778913 | BRCA2 | c.3960A>C (p.Glu1320Asp) c.3591A>C (p.Glu1197Asp) n.3960A>C | ClinVar |
| 13 | g.32338315A>G | CA483437949 | BRCA2 | c.3960A>G (p.Glu1320=) c.3591A>G (p.Glu1197=) n.3960A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338315A>T | CA387778914 | BRCA2 | c.3960A>T (p.Glu1320Asp) c.3591A>T (p.Glu1197Asp) n.3960A>T | dbSNP gnomAD v4 |
| 13 | g.32338316_32338326del | CA2697551724 | BRCA2 | c.3961_3971del (p.Asp1321TyrfsTer5) c.3592_3602del (p.Asp1198TyrfsTer5) n.3961_3971del | ClinVar |
| 13 | g.32338316G>A | CA6940736 | BRCA2 | c.3961G>A (p.Asp1321Asn) c.3592G>A (p.Asp1198Asn) n.3961G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338316G>C | CA6940735 | BRCA2 | c.3961G>C (p.Asp1321His) c.3592G>C (p.Asp1198His) n.3961G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338316G= | CA2082822467 | BRCA2 | c.3961G= (p.Asp1321=) c.3592G= (p.Asp1198=) n.3961G= | |
| 13 | g.32338316G>T | CA387778915 | BRCA2 | c.3961G>T (p.Asp1321Tyr) c.3592G>T (p.Asp1198Tyr) n.3961G>T | dbSNP |
| 13 | g.32338317A= | CA2082822469 | BRCA2 | c.3962A= (p.Asp1321=) c.3593A= (p.Asp1198=) n.3962A= | |
| 13 | g.32338317A>C | CA387778916 | BRCA2 | c.3962A>C (p.Asp1321Ala) c.3593A>C (p.Asp1198Ala) n.3962A>C | |
| 13 | g.32338317A>G | CA019277 | BRCA2 | c.3962A>G (p.Asp1321Gly) c.3593A>G (p.Asp1198Gly) n.3962A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338317A>T | CA247506226 | BRCA2 | c.3962A>T (p.Asp1321Val) c.3593A>T (p.Asp1198Val) n.3962A>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338318T>A | CA387778917 | BRCA2 | c.3963T>A (p.Asp1321Glu) c.3594T>A (p.Asp1198Glu) n.3963T>A | dbSNP |
| 13 | g.32338318T>C | CA483437956 | BRCA2 | c.3963T>C (p.Asp1321=) c.3594T>C (p.Asp1198=) n.3963T>C | ClinVar dbSNP |
| 13 | g.32338318T>G | CA387778918 | BRCA2 | c.3963T>G (p.Asp1321Glu) c.3594T>G (p.Asp1198Glu) n.3963T>G | dbSNP |
| 13 | g.32338318_32338321delinsTAAC | CA2082822473 | BRCA2 | c.3963_3966delinsTAAC (p.Asp1321=) c.3594_3597delinsTAAC (p.Asp1198=) n.3963_3966delinsTAAC | |
| 13 | g.32338319A= | CA2082822483 | BRCA2 | c.3964A= (p.Asn1322=) c.3595A= (p.Asn1199=) n.3964A= | |
| 13 | g.32338319A>C | CA387778920 | BRCA2 | c.3964A>C (p.Asn1322His) c.3595A>C (p.Asn1199His) n.3964A>C | ClinVar dbSNP |
| 13 | g.32338319A>G | CA10586065 | BRCA2 | c.3964A>G (p.Asn1322Asp) c.3595A>G (p.Asn1199Asp) n.3964A>G | ClinVar dbSNP |
| 13 | g.32338319A>T | CA387778919 | BRCA2 | c.3964A>T (p.Asn1322Tyr) c.3595A>T (p.Asn1199Tyr) n.3964A>T | dbSNP |
| 13 | g.32338321_32338323del | CA019288 | BRCA2 | c.3966_3968del (p.Asn1322del) c.3597_3599del (p.Asn1199del) n.3966_3968del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338320A= | CA2082822500 | BRCA2 | c.3965A= (p.Asn1322=) c.3596A= (p.Asn1199=) n.3965A= | |
| 13 | g.32338320A>C | CA019283 | BRCA2 | c.3965A>C (p.Asn1322Thr) c.3596A>C (p.Asn1199Thr) n.3965A>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338320A>G | CA387778921 | BRCA2 | c.3965A>G (p.Asn1322Ser) c.3596A>G (p.Asn1199Ser) n.3965A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338320A>T | CA387778922 | BRCA2 | c.3965A>T (p.Asn1322Ile) c.3596A>T (p.Asn1199Ile) n.3965A>T | dbSNP |
| 13 | g.32338321C>A | CA387778923 | BRCA2 | c.3966C>A (p.Asn1322Lys) c.3597C>A (p.Asn1199Lys) n.3966C>A | dbSNP gnomAD v4 |
| 13 | g.32338321C= | CA2082822520 | BRCA2 | c.3966C= (p.Asn1322=) c.3597C= (p.Asn1199=) n.3966C= | |
| 13 | g.32338321C>G | CA019298 | BRCA2 | c.3966C>G (p.Asn1322Lys) c.3597C>G (p.Asn1199Lys) n.3966C>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338321C>T | CA019300 | BRCA2 | c.3966C>T (p.Asn1322=) c.3597C>T (p.Asn1199=) n.3966C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338321_32338325delinsCAAAT | CA2082822513 | BRCA2 | c.3966_3970delinsCAAAT (p.Asn1322=) c.3597_3601delinsCAAAT (p.Asn1199=) n.3966_3970delinsCAAAT | |
| 13 | g.32338322A= | CA2082822530 | BRCA2 | c.3967A= (p.Lys1323=) c.3598A= (p.Lys1200=) n.3967A= | |
| 13 | g.32338322A>C | CA387778924 | BRCA2 | c.3967A>C (p.Lys1323Gln) c.3598A>C (p.Lys1200Gln) n.3967A>C | ClinVar |
| 13 | g.32338322A>G | CA387778925 | BRCA2 | c.3967A>G (p.Lys1323Glu) c.3598A>G (p.Lys1200Glu) n.3967A>G | ClinVar dbSNP |
| 13 | g.32338322A>T | CA019306 | BRCA2 | c.3967A>T (p.Lys1323Ter) c.3598A>T (p.Lys1200Ter) n.3967A>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338323_32338324del | CA2499222149 | BRCA2 | c.3968_3969del (p.Lys1323IlefsTer6) c.3599_3600del (p.Lys1200IlefsTer6) n.3968_3969del | ClinVar dbSNP |
| 13 | g.32338323_32338326del | CA10589233 | BRCA2 | c.3968_3971del (p.Lys1323IlefsTer11) c.3599_3602del (p.Lys1200IlefsTer11) n.3968_3971del | ClinVar dbSNP |
| 13 | g.32338323A= | CA2082822542 | BRCA2 | c.3968A= (p.Lys1323=) c.3599A= (p.Lys1200=) n.3968A= | |
| 13 | g.32338323A>C | CA387778928 | BRCA2 | c.3968A>C (p.Lys1323Thr) c.3599A>C (p.Lys1200Thr) n.3968A>C | |
| 13 | g.32338323A>G | CA387778927 | BRCA2 | c.3968A>G (p.Lys1323Arg) c.3599A>G (p.Lys1200Arg) n.3968A>G | ClinVar dbSNP |
| 13 | g.32338323A>T | CA387778926 | BRCA2 | c.3968A>T (p.Lys1323Ile) c.3599A>T (p.Lys1200Ile) n.3968A>T | dbSNP |
| 13 | g.32338323_32338325delinsAAT | CA2082822541 | BRCA2 | c.3968_3970delinsAAT (p.Lys1323=) c.3599_3601delinsAAT (p.Lys1200=) n.3968_3970delinsAAT | |
| 13 | g.32338324A= | CA2082822557 | BRCA2 | c.3969A= (p.Lys1323=) c.3600A= (p.Lys1200=) n.3969A= | |
| 13 | g.32338324A>C | CA387778929 | BRCA2 | c.3969A>C (p.Lys1323Asn) c.3600A>C (p.Lys1200Asn) n.3969A>C | |
| 13 | g.32338324A>G | CA483437968 | BRCA2 | c.3969A>G (p.Lys1323=) c.3600A>G (p.Lys1200=) n.3969A>G | ClinVar dbSNP |
| 13 | g.32338324A>T | CA387778930 | BRCA2 | c.3969A>T (p.Lys1323Asn) c.3600A>T (p.Lys1200Asn) n.3969A>T | |
| 13 | g.32338327_32338328del | CA10589234 | BRCA2 | c.3972_3973del (p.Thr1325CysfsTer4) c.3603_3604del (p.Thr1202CysfsTer4) n.3972_3973del | ClinVar dbSNP |
| 13 | g.32338324_32338325insCT | CA913188551 | BRCA2 | c.3969_3970insCT (p.Tyr1324LeufsTer12) c.3600_3601insCT (p.Tyr1201LeufsTer12) n.3969_3970insCT | ClinVar |
| 13 | g.32338325T>A | CA387778931 | BRCA2 | c.3970T>A (p.Tyr1324Asn) c.3601T>A (p.Tyr1201Asn) n.3970T>A | dbSNP |
| 13 | g.32338325T>C | CA10584444 | BRCA2 | c.3970T>C (p.Tyr1324His) c.3601T>C (p.Tyr1201His) n.3970T>C | ClinVar dbSNP |
| 13 | g.32338325T>G | CA387778932 | BRCA2 | c.3970T>G (p.Tyr1324Asp) c.3601T>G (p.Tyr1201Asp) n.3970T>G | dbSNP |
| 13 | g.32338325T= | CA2082822565 | BRCA2 | c.3970T= (p.Tyr1324=) c.3601T= (p.Tyr1201=) n.3970T= | |
| 13 | g.32338325_32338326delinsTA | CA2082822562 | BRCA2 | c.3970_3971delinsTA (p.Tyr1324=) c.3601_3602delinsTA (p.Tyr1201=) n.3970_3971delinsTA | |
| 13 | g.32338326del | CA658761227 | BRCA2 | c.3971del (p.Tyr1324LeufsTer11) c.3602del (p.Tyr1201LeufsTer11) n.3971del | ClinVar dbSNP |
| 13 | g.32338326A= | CA2082822588 | BRCA2 | c.3971A= (p.Tyr1324=) c.3602A= (p.Tyr1201=) n.3971A= | |
| 13 | g.32338326A>C | CA387778933 | BRCA2 | c.3971A>C (p.Tyr1324Ser) c.3602A>C (p.Tyr1201Ser) n.3971A>C | ClinVar dbSNP |
| 13 | g.32338326A>G | CA387778934 | BRCA2 | c.3971A>G (p.Tyr1324Cys) c.3602A>G (p.Tyr1201Cys) n.3971A>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338326A>T | CA387778935 | BRCA2 | c.3971A>T (p.Tyr1324Phe) c.3602A>T (p.Tyr1201Phe) n.3971A>T | |
| 13 | g.32338326_32338330delinsATACT | CA2082822578 | BRCA2 | c.3971_3975delinsATACT (p.Tyr1324=) c.3602_3606delinsATACT (p.Tyr1201=) n.3971_3975delinsATACT | |
| 13 | g.32338327T>A | CA387778936 | BRCA2 | c.3972T>A (p.Tyr1324Ter) c.3603T>A (p.Tyr1201Ter) n.3972T>A | dbSNP gnomAD v4 |
| 13 | g.32338327T>C | CA483437973 | BRCA2 | c.3972T>C (p.Tyr1324=) c.3603T>C (p.Tyr1201=) n.3972T>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32338327T>G | CA387778937 | BRCA2 | c.3972T>G (p.Tyr1324Ter) c.3603T>G (p.Tyr1201Ter) n.3972T>G | ClinVar dbSNP |
| 13 | g.32338327T= | CA2082822600 | BRCA2 | c.3972T= (p.Tyr1324=) c.3603T= (p.Tyr1201=) n.3972T= | |
| 13 | g.32338327_32338330del | CA10589235 | BRCA2 | c.3972_3975del (p.Tyr1324Ter) c.3603_3606del (p.Tyr1201Ter) n.3972_3975del | ClinVar dbSNP |
| 13 | g.32338328A>C | CA387778939 | BRCA2 | c.3973A>C (p.Thr1325Pro) c.3604A>C (p.Thr1202Pro) n.3973A>C | dbSNP |
| 13 | g.32338328A>G | CA387778940 | BRCA2 | c.3973A>G (p.Thr1325Ala) c.3604A>G (p.Thr1202Ala) n.3973A>G | ClinVar |
| 13 | g.32338328A>T | CA387778938 | BRCA2 | c.3973A>T (p.Thr1325Ser) c.3604A>T (p.Thr1202Ser) n.3973A>T | dbSNP |
| 13 | g.32338329C>A | CA387778942 | BRCA2 | c.3974C>A (p.Thr1325Asn) c.3605C>A (p.Thr1202Asn) n.3974C>A | |
| 13 | g.32338329C= | CA2082822617 | BRCA2 | c.3974C= (p.Thr1325=) c.3605C= (p.Thr1202=) n.3974C= | |
| 13 | g.32338329C>G | CA387778941 | BRCA2 | c.3974C>G (p.Thr1325Ser) c.3605C>G (p.Thr1202Ser) n.3974C>G | ClinVar dbSNP |
| 13 | g.32338329C>T | CA387778943 | BRCA2 | c.3974C>T (p.Thr1325Ile) c.3605C>T (p.Thr1202Ile) n.3974C>T | ClinVar dbSNP |
| 13 | g.32338330T>A | CA483437978 | BRCA2 | c.3975T>A (p.Thr1325=) c.3606T>A (p.Thr1202=) n.3975T>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338330T>C | CA16606681 | BRCA2 | c.3975T>C (p.Thr1325=) c.3606T>C (p.Thr1202=) n.3975T>C | ClinVar dbSNP |
| 13 | g.32338330T>G | CA483437977 | BRCA2 | c.3975T>G (p.Thr1325=) c.3606T>G (p.Thr1202=) n.3975T>G | |
| 13 | g.32338330T= | CA2082822624 | BRCA2 | c.3975T= (p.Thr1325=) c.3606T= (p.Thr1202=) n.3975T= | |
| 13 | g.32338330_32338333dup | CA019317 | BRCA2 | c.3975_3978dup (p.Ala1327CysfsTer4) c.3606_3609dup (p.Ala1204CysfsTer4) n.3975_3978dup | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338331G>A | CA387778944 | BRCA2 | c.3976G>A (p.Ala1326Thr) c.3607G>A (p.Ala1203Thr) n.3976G>A | dbSNP |
| 13 | g.32338331G>C | CA387778945 | BRCA2 | c.3976G>C (p.Ala1326Pro) c.3607G>C (p.Ala1203Pro) n.3976G>C | dbSNP |
| 13 | g.32338331G>T | CA387778946 | BRCA2 | c.3976G>T (p.Ala1326Ser) c.3607G>T (p.Ala1203Ser) n.3976G>T | dbSNP |
| 13 | g.32338332C>A | CA387778947 | BRCA2 | c.3977C>A (p.Ala1326Asp) c.3608C>A (p.Ala1203Asp) n.3977C>A | dbSNP |
| 13 | g.32338332C>G | CA387778948 | BRCA2 | c.3977C>G (p.Ala1326Gly) c.3608C>G (p.Ala1203Gly) n.3977C>G | dbSNP |
| 13 | g.32338332C>T | CA387778949 | BRCA2 | c.3977C>T (p.Ala1326Val) c.3608C>T (p.Ala1203Val) n.3977C>T | dbSNP |
| 13 | g.32338333T>A | CA483437981 | BRCA2 | c.3978T>A (p.Ala1326=) c.3609T>A (p.Ala1203=) n.3978T>A | dbSNP |
| 13 | g.32338333T>C | CA483437982 | BRCA2 | c.3978T>C (p.Ala1326=) c.3609T>C (p.Ala1203=) n.3978T>C | ClinVar gnomAD v4 |
| 13 | g.32338333T>G | CA483437983 | BRCA2 | c.3978T>G (p.Ala1326=) c.3609T>G (p.Ala1203=) n.3978T>G | dbSNP |
| 13 | g.32338333T= | CA2082822638 | BRCA2 | c.3978T= (p.Ala1326=) c.3609T= (p.Ala1203=) n.3978T= | |
| 13 | g.32338333_32338334insTTGC | CA10589236 | BRCA2 | c.3978_3979insTTGC (p.Ala1327LeufsTer4) c.3609_3610insTTGC (p.Ala1204LeufsTer4) n.3978_3979insTTGC | ClinVar dbSNP |
| 13 | g.32338334G>A | CA387778950 | BRCA2 | c.3979G>A (p.Ala1327Thr) c.3610G>A (p.Ala1204Thr) n.3979G>A | |
| 13 | g.32338334G>C | CA387778951 | BRCA2 | c.3979G>C (p.Ala1327Pro) c.3610G>C (p.Ala1204Pro) n.3979G>C | |
| 13 | g.32338334G= | CA2082822643 | BRCA2 | c.3979G= (p.Ala1327=) c.3610G= (p.Ala1204=) n.3979G= | |
| 13 | g.32338334G>T | CA387778952 | BRCA2 | c.3979G>T (p.Ala1327Ser) c.3610G>T (p.Ala1204Ser) n.3979G>T | ClinVar dbSNP |
| 13 | g.32338335C>A | CA387778955 | BRCA2 | c.3980C>A (p.Ala1327Asp) c.3611C>A (p.Ala1204Asp) n.3980C>A | dbSNP |
| 13 | g.32338335C>G | CA387778953 | BRCA2 | c.3980C>G (p.Ala1327Gly) c.3611C>G (p.Ala1204Gly) n.3980C>G | dbSNP |
| 13 | g.32338335C>T | CA387778954 | BRCA2 | c.3980C>T (p.Ala1327Val) c.3611C>T (p.Ala1204Val) n.3980C>T | dbSNP |
| 13 | g.32338336C>A | CA483437985 | BRCA2 | c.3981C>A (p.Ala1327=) c.3612C>A (p.Ala1204=) n.3981C>A | ClinVar dbSNP |
| 13 | g.32338336C= | CA2082822647 | BRCA2 | c.3981C= (p.Ala1327=) c.3612C= (p.Ala1204=) n.3981C= | |
| 13 | g.32338336C>G | CA483437986 | BRCA2 | c.3981C>G (p.Ala1327=) c.3612C>G (p.Ala1204=) n.3981C>G | dbSNP |
| 13 | g.32338336C>T | CA483437987 | BRCA2 | c.3981C>T (p.Ala1327=) c.3612C>T (p.Ala1204=) n.3981C>T | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338337A= | CA2082822656 | BRCA2 | c.3982A= (p.Ser1328=) c.3613A= (p.Ser1205=) n.3982A= | |
| 13 | g.32338337A>C | CA387778956 | BRCA2 | c.3982A>C (p.Ser1328Arg) c.3613A>C (p.Ser1205Arg) n.3982A>C | |
| 13 | g.32338337A>G | CA387778957 | BRCA2 | c.3982A>G (p.Ser1328Gly) c.3613A>G (p.Ser1205Gly) n.3982A>G | ClinVar dbSNP |
| 13 | g.32338337A>T | CA387778958 | BRCA2 | c.3982A>T (p.Ser1328Cys) c.3613A>T (p.Ser1205Cys) n.3982A>T | ClinVar dbSNP |
| 13 | g.32338338G>A | CA6940737 | BRCA2 | c.3983G>A (p.Ser1328Asn) c.3614G>A (p.Ser1205Asn) n.3983G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338338G>C | CA10579597 | BRCA2 | c.3983G>C (p.Ser1328Thr) c.3614G>C (p.Ser1205Thr) n.3983G>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338338G= | CA2082822663 | BRCA2 | c.3983G= (p.Ser1328=) c.3614G= (p.Ser1205=) n.3983G= | |
| 13 | g.32338338G>T | CA387778959 | BRCA2 | c.3983G>T (p.Ser1328Ile) c.3614G>T (p.Ser1205Ile) n.3983G>T | |
| 13 | g.32338339T>A | CA387778960 | BRCA2 | c.3984T>A (p.Ser1328Arg) c.3615T>A (p.Ser1205Arg) n.3984T>A | dbSNP |
| 13 | g.32338339T>C | CA10579598 | BRCA2 | c.3984T>C (p.Ser1328=) c.3615T>C (p.Ser1205=) n.3984T>C | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32338339T>G | CA387778961 | BRCA2 | c.3984T>G (p.Ser1328Arg) c.3615T>G (p.Ser1205Arg) n.3984T>G | dbSNP |
| 13 | g.32338339T= | CA2082822681 | BRCA2 | c.3984T= (p.Ser1328=) c.3615T= (p.Ser1205=) n.3984T= | |
| 13 | g.32338340A= | CA2082822686 | BRCA2 | c.3985A= (p.Arg1329=) c.3616A= (p.Arg1206=) n.3985A= | |
| 13 | g.32338340A>C | CA483437994 | BRCA2 | c.3985A>C (p.Arg1329=) c.3616A>C (p.Arg1206=) n.3985A>C | |
| 13 | g.32338340A>G | CA019330 | BRCA2 | c.3985A>G (p.Arg1329Gly) c.3616A>G (p.Arg1206Gly) n.3985A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338340A>T | CA387778962 | BRCA2 | c.3985A>T (p.Arg1329Ter) c.3616A>T (p.Arg1206Ter) n.3985A>T | dbSNP |
| 13 | g.32338341G>A | CA387778965 | BRCA2 | c.3986G>A (p.Arg1329Lys) c.3617G>A (p.Arg1206Lys) n.3986G>A | ClinVar dbSNP |
| 13 | g.32338341G>C | CA387778964 | BRCA2 | c.3986G>C (p.Arg1329Thr) c.3617G>C (p.Arg1206Thr) n.3986G>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338341G= | CA2082822692 | BRCA2 | c.3986G= (p.Arg1329=) c.3617G= (p.Arg1206=) n.3986G= | |
| 13 | g.32338341G>T | CA387778963 | BRCA2 | c.3986G>T (p.Arg1329Ile) c.3617G>T (p.Arg1206Ile) n.3986G>T | ClinVar dbSNP |
| 13 | g.32338342A= | CA2082822698 | BRCA2 | c.3987A= (p.Arg1329=) c.3618A= (p.Arg1206=) n.3987A= | |
| 13 | g.32338342A>C | CA387778966 | BRCA2 | c.3987A>C (p.Arg1329Ser) c.3618A>C (p.Arg1206Ser) n.3987A>C | |
| 13 | g.32338342A>G | CA483437997 | BRCA2 | c.3987A>G (p.Arg1329=) c.3618A>G (p.Arg1206=) n.3987A>G | ClinVar |
| 13 | g.32338342A>T | CA019337 | BRCA2 | c.3987A>T (p.Arg1329Ser) c.3618A>T (p.Arg1206Ser) n.3987A>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338343A>C | CA387778967 | BRCA2 | c.3988A>C (p.Asn1330His) c.3619A>C (p.Asn1207His) n.3988A>C | ClinVar |
| 13 | g.32338343A>G | CA387778968 | BRCA2 | c.3988A>G (p.Asn1330Asp) c.3619A>G (p.Asn1207Asp) n.3988A>G | |
| 13 | g.32338343A>T | CA387778969 | BRCA2 | c.3988A>T (p.Asn1330Tyr) c.3619A>T (p.Asn1207Tyr) n.3988A>T | |
| 13 | g.32338344A= | CA2082822711 | BRCA2 | c.3989A= (p.Asn1330=) c.3620A= (p.Asn1207=) n.3989A= | |
| 13 | g.32338344A>C | CA387778970 | BRCA2 | c.3989A>C (p.Asn1330Thr) c.3620A>C (p.Asn1207Thr) n.3989A>C | |
| 13 | g.32338344A>G | CA16607464 | BRCA2 | c.3989A>G (p.Asn1330Ser) c.3620A>G (p.Asn1207Ser) n.3989A>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338344A>T | CA387778971 | BRCA2 | c.3989A>T (p.Asn1330Ile) c.3620A>T (p.Asn1207Ile) n.3989A>T | ClinVar dbSNP |
| 13 | g.32338345T>A | CA387778972 | BRCA2 | c.3990T>A (p.Asn1330Lys) c.3621T>A (p.Asn1207Lys) n.3990T>A | |
| 13 | g.32338345T>C | CA483438001 | BRCA2 | c.3990T>C (p.Asn1330=) c.3621T>C (p.Asn1207=) n.3990T>C | |
| 13 | g.32338345T>G | CA387778973 | BRCA2 | c.3990T>G (p.Asn1330Lys) c.3621T>G (p.Asn1207Lys) n.3990T>G | dbSNP |
| 13 | g.32338346dup | CA2499222150 | BRCA2 | c.3991dup (p.Ser1331PhefsTer3) c.3622dup (p.Ser1208PhefsTer3) n.3991dup | ClinVar dbSNP |
| 13 | g.32338346T>A | CA387778974 | BRCA2 | c.3991T>A (p.Ser1331Thr) c.3622T>A (p.Ser1208Thr) n.3991T>A | ClinVar dbSNP |
| 13 | g.32338346T>C | CA387778975 | BRCA2 | c.3991T>C (p.Ser1331Pro) c.3622T>C (p.Ser1208Pro) n.3991T>C | dbSNP |
| 13 | g.32338346T>G | CA387778976 | BRCA2 | c.3991T>G (p.Ser1331Ala) c.3622T>G (p.Ser1208Ala) n.3991T>G | |
| 13 | g.32338347C>A | CA387778979 | BRCA2 | c.3992C>A (p.Ser1331Tyr) c.3623C>A (p.Ser1208Tyr) n.3992C>A | dbSNP |
| 13 | g.32338347C>G | CA387778977 | BRCA2 | c.3992C>G (p.Ser1331Cys) c.3623C>G (p.Ser1208Cys) n.3992C>G | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338347C>T | CA387778978 | BRCA2 | c.3992C>T (p.Ser1331Phe) c.3623C>T (p.Ser1208Phe) n.3992C>T | dbSNP |
| 13 | g.32338348T>A | CA483438006 | BRCA2 | c.3993T>A (p.Ser1331=) c.3624T>A (p.Ser1208=) n.3993T>A | dbSNP |
| 13 | g.32338348T>C | CA6940738 | BRCA2 | c.3993T>C (p.Ser1331=) c.3624T>C (p.Ser1208=) n.3993T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338348T>G | CA483438005 | BRCA2 | c.3993T>G (p.Ser1331=) c.3624T>G (p.Ser1208=) n.3993T>G | |
| 13 | g.32338348T= | CA2082822722 | BRCA2 | c.3993T= (p.Ser1331=) c.3624T= (p.Ser1208=) n.3993T= | |
| 13 | g.32338349C>A | CA387778980 | BRCA2 | c.3994C>A (p.His1332Asn) c.3625C>A (p.His1209Asn) n.3994C>A | dbSNP |
| 13 | g.32338349C= | CA2082822734 | BRCA2 | c.3994C= (p.His1332=) c.3625C= (p.His1209=) n.3994C= | |
| 13 | g.32338349C>G | CA16619701 | BRCA2 | c.3994C>G (p.His1332Asp) c.3625C>G (p.His1209Asp) n.3994C>G | ClinVar dbSNP |
| 13 | g.32338349C>T | CA336760 | BRCA2 | c.3994C>T (p.His1332Tyr) c.3625C>T (p.His1209Tyr) n.3994C>T | ClinVar dbSNP COSMIC COSMIC |
| 13 | g.32338350A= | CA2082822743 | BRCA2 | c.3995A= (p.His1332=) c.3626A= (p.His1209=) n.3995A= | |
| 13 | g.32338350A>C | CA387778981 | BRCA2 | c.3995A>C (p.His1332Pro) c.3626A>C (p.His1209Pro) n.3995A>C | |
| 13 | g.32338350A>G | CA019343 | BRCA2 | c.3995A>G (p.His1332Arg) c.3626A>G (p.His1209Arg) n.3995A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338350A>T | CA387778982 | BRCA2 | c.3995A>T (p.His1332Leu) c.3626A>T (p.His1209Leu) n.3995A>T | dbSNP |
| 13 | g.32338351T>A | CA387778983 | BRCA2 | c.3996T>A (p.His1332Gln) c.3627T>A (p.His1209Gln) n.3996T>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32338351T>C | CA483438010 | BRCA2 | c.3996T>C (p.His1332=) c.3627T>C (p.His1209=) n.3996T>C | ClinVar dbSNP |
| 13 | g.32338351T>G | CA387778984 | BRCA2 | c.3996T>G (p.His1332Gln) c.3627T>G (p.His1209Gln) n.3996T>G | ClinVar dbSNP |
| 13 | g.32338351T= | CA2082822748 | BRCA2 | c.3996T= (p.His1332=) c.3627T= (p.His1209=) n.3996T= | |
| 13 | g.32338353_32338357del | CA2573149358 | BRCA2 | c.3998_4002del (p.Asn1333ArgfsTer3) c.3629_3633del (p.Asn1210ArgfsTer3) n.3998_4002del | ClinVar dbSNP |
| 13 | g.32338352A= | CA2082822758 | BRCA2 | c.3997A= (p.Asn1333=) c.3628A= (p.Asn1210=) n.3997A= | |
| 13 | g.32338352A>C | CA387778985 | BRCA2 | c.3997A>C (p.Asn1333His) c.3628A>C (p.Asn1210His) n.3997A>C | |
| 13 | g.32338352A>G | CA387778986 | BRCA2 | c.3997A>G (p.Asn1333Asp) c.3628A>G (p.Asn1210Asp) n.3997A>G | |
| 13 | g.32338352A>T | CA387778987 | BRCA2 | c.3997A>T (p.Asn1333Tyr) c.3628A>T (p.Asn1210Tyr) n.3997A>T | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338354_32338360del | CA2580087234 | BRCA2 | c.3999_4005del (p.Glu1335MetfsTer?) c.3630_3636del (p.Glu1212MetfsTer?) n.3999_4005del | ClinVar |
| 13 | g.32338353A>C | CA387778990 | BRCA2 | c.3998A>C (p.Asn1333Thr) c.3629A>C (p.Asn1210Thr) n.3998A>C | |
| 13 | g.32338353A>G | CA387778989 | BRCA2 | c.3998A>G (p.Asn1333Ser) c.3629A>G (p.Asn1210Ser) n.3998A>G | dbSNP |
| 13 | g.32338353A>T | CA387778988 | BRCA2 | c.3998A>T (p.Asn1333Ile) c.3629A>T (p.Asn1210Ile) n.3998A>T | dbSNP |
| 13 | g.32338354C>A | CA387778991 | BRCA2 | c.3999C>A (p.Asn1333Lys) c.3630C>A (p.Asn1210Lys) n.3999C>A | |
| 13 | g.32338354C= | CA2082822765 | BRCA2 | c.3999C= (p.Asn1333=) c.3630C= (p.Asn1210=) n.3999C= | |
| 13 | g.32338354C>G | CA019346 | BRCA2 | c.3999C>G (p.Asn1333Lys) c.3630C>G (p.Asn1210Lys) n.3999C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.32338354C>T | CA483438014 | BRCA2 | c.3999C>T (p.Asn1333=) c.3630C>T (p.Asn1210=) n.3999C>T | ClinVar gnomAD v4 |
| 13 | g.32338354_32338356delinsCTT | CA2082822773 | BRCA2 | c.3999_4001delinsCTT (p.Asn1333=) c.3630_3632delinsCTT (p.Asn1210=) n.3999_4001delinsCTT |