Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.40072292A= | CA2425444173 | BCOR | c.2997+57T= (n.2997+57T=) n.3094T= c.*39T= (n.*39T=) | |
X | g.40072292A>G | CA2425444174 | BCOR | c.2997+57T>C (n.2997+57T>C) n.3094T>C c.*39T>C (n.*39T>C) | dbSNP gnomAD v3 gnomAD v4 |
X | g.40072292A>T | CA2693454656 | BCOR | c.2997+57T>A (n.2997+57T>A) n.3094T>A c.*39T>A (n.*39T>A) | gnomAD v4 |
X | g.40072293C>G | CA2555172090 | BCOR | c.2997+56G>C (n.2997+56G>C) n.3093G>C c.*38G>C (n.*38G>C) | |
X | g.40072293C>T | CA2693454657 | BCOR | c.2997+56G>A (n.2997+56G>A) n.3093G>A c.*38G>A (n.*38G>A) | gnomAD v4 |
X | g.40072294A>C | CA2579585691 | BCOR | c.2997+55T>G (n.2997+55T>G) n.3092T>G c.*37T>G (n.*37T>G) | gnomAD v4 |
X | g.40072295C= | CA2425444175 | BCOR | c.2997+54G= (n.2997+54G=) n.3091G= c.*36G= (n.*36G=) | |
X | g.40072295C>G | CA875271225 | BCOR | c.2997+54G>C (n.2997+54G>C) n.3091G>C c.*36G>C (n.*36G>C) | dbSNP |
X | g.40072295C>T | CA2693454658 | BCOR | c.2997+54G>A (n.2997+54G>A) n.3091G>A c.*36G>A (n.*36G>A) | gnomAD v4 |
X | g.40072297T>G | CA875271232 | BCOR | c.2997+52A>C (n.2997+52A>C) n.3089A>C c.*34A>C (n.*34A>C) | dbSNP gnomAD v3 gnomAD v4 |
X | g.40072297T= | CA2425444176 | BCOR | c.2997+52A= (n.2997+52A=) n.3089A= c.*34A= (n.*34A=) | |
X | g.40072298T>A | CA2425444178 | BCOR | c.2997+51A>T (n.2997+51A>T) n.3088A>T c.*33A>T (n.*33A>T) | dbSNP |
X | g.40072298T= | CA2425444177 | BCOR | c.2997+51A= (n.2997+51A=) n.3088A= c.*33A= (n.*33A=) | |
X | g.40072300A>C | CA2693454659 | BCOR | c.2997+49T>G (n.2997+49T>G) n.3086T>G c.*31T>G (n.*31T>G) | gnomAD v4 |
X | g.40072302A= | CA2425444179 | BCOR | c.2997+47T= (n.2997+47T=) n.3084T= c.*29T= (n.*29T=) | |
X | g.40072302A>G | CA10386720 | BCOR | c.2997+47T>C (n.2997+47T>C) n.3084T>C c.*29T>C (n.*29T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.40072307G>A | CA2693454660 | BCOR | c.2997+42C>T (n.2997+42C>T) n.3079C>T c.*24C>T (n.*24C>T) | dbSNP gnomAD v4 |
X | g.40072307G>C | CA2738464750 | BCOR | c.2997+42C>G (n.2997+42C>G) n.3079C>G c.*24C>G (n.*24C>G) | dbSNP |
X | g.40072307G>T | CA2579585692 | BCOR | c.2997+42C>A (n.2997+42C>A) n.3079C>A c.*24C>A (n.*24C>A) | |
X | g.40072309C= | CA2425444180 | BCOR | c.2997+40G= (n.2997+40G=) n.3077G= c.*22G= (n.*22G=) | |
X | g.40072309C>G | CA657837817 | BCOR | c.2997+40G>C (n.2997+40G>C) n.3077G>C c.*22G>C (n.*22G>C) | gnomAD v4 COSMIC |
X | g.40072309C>T | CA641363330 | BCOR | c.2997+40G>A (n.2997+40G>A) n.3077G>A c.*22G>A (n.*22G>A) | dbSNP gnomAD v2 gnomAD v4 |
X | g.40072311A>G | CA2693454661 | BCOR | c.2997+38T>C (n.2997+38T>C) n.3075T>C c.*20T>C (n.*20T>C) | gnomAD v4 |
X | g.40072311A>T | CA2558742550 | BCOR | c.2997+38T>A (n.2997+38T>A) n.3075T>A c.*20T>A (n.*20T>A) | |
X | g.40072313T>C | CA2693454662 | BCOR | c.2997+36A>G (n.2997+36A>G) n.3073A>G c.*18A>G (n.*18A>G) | gnomAD v4 |
X | g.40072314G>T | CA2693454663 | BCOR | c.2997+35C>A (n.2997+35C>A) n.3072C>A c.*17C>A (n.*17C>A) | gnomAD v4 |
X | g.40072315G>A | CA327991330 | BCOR | c.2997+34C>T (n.2997+34C>T) n.3071C>T c.*16C>T (n.*16C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.40072315G>C | CA2693454664 | BCOR | c.2997+34C>G (n.2997+34C>G) n.3071C>G c.*16C>G (n.*16C>G) | gnomAD v4 |
X | g.40072315G= | CA2425444181 | BCOR | c.2997+34C= (n.2997+34C=) n.3071C= c.*16C= (n.*16C=) | |
X | g.40072315G>T | CA2534302831 | BCOR | c.2997+34C>A (n.2997+34C>A) n.3071C>A c.*16C>A (n.*16C>A) | gnomAD v4 |
X | g.40072316T>C | CA2693454665 | BCOR | c.2997+33A>G (n.2997+33A>G) n.3070A>G c.*15A>G (n.*15A>G) | gnomAD v4 |
X | g.40072317A>G | CA2693454666 | BCOR | c.2997+32T>C (n.2997+32T>C) n.3069T>C c.*14T>C (n.*14T>C) | gnomAD v4 |
X | g.40072320G>T | CA2579585693 | BCOR | c.2997+29C>A (n.2997+29C>A) n.3066C>A c.*11C>A (n.*11C>A) | |
X | g.40072321T>C | CA327991331 | BCOR | c.2997+28A>G (n.2997+28A>G) n.3065A>G c.*10A>G (n.*10A>G) | dbSNP gnomAD v2 gnomAD v4 |
X | g.40072321T= | CA2425444182 | BCOR | c.2997+28A= (n.2997+28A=) n.3065A= c.*10A= (n.*10A=) | |
X | g.40072322A>G | CA657837818 | BCOR | c.2997+27T>C (n.2997+27T>C) n.3064T>C c.*9T>C (n.*9T>C) | COSMIC |
X | g.40072326G>A | CA2693454667 | BCOR | c.2997+23C>T (n.2997+23C>T) n.3060C>T c.*5C>T (n.*5C>T) | gnomAD v4 |
X | g.40072326G= | CA2425444183 | BCOR | c.2997+23C= (n.2997+23C=) n.3060C= c.*5C= (n.*5C=) | |
X | g.40072326G>T | CA641363331 | BCOR | c.2997+23C>A (n.2997+23C>A) n.3060C>A c.*5C>A (n.*5C>A) | dbSNP gnomAD v2 gnomAD v4 |
X | g.40072327A= | CA2425444184 | BCOR | c.2997+22T= (n.2997+22T=) n.3059T= c.*4T= (n.*4T=) | |
X | g.40072327A>T | CA641363332 | BCOR | c.2997+22T>A (n.2997+22T>A) n.3059T>A c.*4T>A (n.*4T>A) | dbSNP gnomAD v2 |
X | g.40072331T>A | CA412740994 | BCOR | c.2997+18A>T (n.2997+18A>T) n.3055A>T c.1236A>T (p.Ter412Cys) | |
X | g.40072331T>C | CA412740995 | BCOR | c.2997+18A>G (n.2997+18A>G) n.3055A>G c.1236A>G (p.Ter412Trp) | |
X | g.40072331T>G | CA412740993 | BCOR | c.2997+18A>C (n.2997+18A>C) n.3055A>C c.1236A>C (p.Ter412Cys) | |
X | g.40072331_40072332insG | CA2579585694 | BCOR | c.2997+17_2997+18insC (n.2997+17_2997+18insC) n.3054_3055insC c.1235_1236insC (p.Ter412CysextTer15) | |
X | g.40072332C>A | CA412740996 | BCOR | c.2997+17G>T (n.2997+17G>T) n.3054G>T c.1235G>T (p.Ter412Leu) | |
X | g.40072332C>G | CA412740997 | BCOR | c.2997+17G>C (n.2997+17G>C) n.3054G>C c.1235G>C (p.Ter412Ser) | |
X | g.40072333A>C | CA412740998 | BCOR | c.2997+16T>G (n.2997+16T>G) n.3053T>G c.1234T>G (p.Ter412Gly) | gnomAD v4 |
X | g.40072333A>G | CA412740999 | BCOR | c.2997+16T>C (n.2997+16T>C) n.3053T>C c.1234T>C (p.Ter412Arg) | gnomAD v4 COSMIC |
X | g.40072333A>T | CA412741000 | BCOR | c.2997+16T>A (n.2997+16T>A) n.3053T>A c.1234T>A (p.Ter412Arg) | |
X | g.40072334G>A | CA2693454668 | BCOR | c.2997+15C>T (n.2997+15C>T) n.3052C>T c.1233C>T (p.Thr411=) | gnomAD v4 |
X | g.40072335G>A | CA412741003 | BCOR | c.2997+14C>T (n.2997+14C>T) n.3051C>T c.1232C>T (p.Thr411Ile) | dbSNP gnomAD v3 gnomAD v4 |
X | g.40072335G>C | CA412741001 | BCOR | c.2997+14C>G (n.2997+14C>G) n.3051C>G c.1232C>G (p.Thr411Ser) | |
X | g.40072335G= | CA2425444185 | BCOR | c.2997+14C= (n.2997+14C=) n.3051C= c.1232C= (p.Thr411=) | |
X | g.40072335G>T | CA412741002 | BCOR | c.2997+14C>A (n.2997+14C>A) n.3051C>A c.1232C>A (p.Thr411Asn) | dbSNP gnomAD v3 gnomAD v4 |
X | g.40072336del | CA2693454669 | BCOR | c.2997+13del (n.2997+13del) n.3050del c.1231del (p.Thr411ProfsTer13) | gnomAD v4 |
X | g.40072336T>A | CA412741004 | BCOR | c.2997+13A>T (n.2997+13A>T) n.3050A>T c.1231A>T (p.Thr411Ser) | |
X | g.40072336T>C | CA412741005 | BCOR | c.2997+13A>G (n.2997+13A>G) n.3050A>G c.1231A>G (p.Thr411Ala) | |
X | g.40072336T>G | CA412741006 | BCOR | c.2997+13A>C (n.2997+13A>C) n.3050A>C c.1231A>C (p.Thr411Pro) | dbSNP |
X | g.40072336T= | CA2425444187 | BCOR | c.2997+13A= (n.2997+13A=) n.3050A= c.1231A= (p.Thr411=) | |
X | g.40072336_40072337delinsTG | CA2425444186 | BCOR | c.2997+12_2997+13delinsCA (n.2997+12_2997+13delinsCA) n.3049_3050delinsCA c.1230_1231delinsCA (p.Pro410=) | |
X | g.40072337G>A | CA2693454670 | BCOR | c.2997+12C>T (n.2997+12C>T) n.3049C>T c.1230C>T (p.Pro410=) | gnomAD v4 |
X | g.40072337G>C | CA10386723 | BCOR | c.2997+12C>G (n.2997+12C>G) n.3049C>G c.1230C>G (p.Pro410=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.40072337G= | CA2425444188 | BCOR | c.2997+12C= (n.2997+12C=) n.3049C= c.1230C= (p.Pro410=) | |
X | g.40072337G>T | CA327991347 | BCOR | c.2997+12C>A (n.2997+12C>A) n.3049C>A c.1230C>A (p.Pro410=) | dbSNP gnomAD v3 gnomAD v4 |
X | g.40072343dup | CA10386722 | BCOR | c.2997+12dup (n.2997+12dup) n.3049dup c.1230dup (p.Thr411HisfsTer16) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.40072342_40072343dup | CA2820522421 | BCOR | c.2997+11_2997+12dup (n.2997+11_2997+12dup) n.3048_3049dup c.1229_1230dup (p.Thr411ProfsTer14) | |
X | g.40072343del | CA10386721 | BCOR | c.2997+12del (n.2997+12del) n.3049del c.1230del (p.Thr411ProfsTer13) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.40072338G>A | CA412741008 | BCOR | c.2997+11C>T (n.2997+11C>T) n.3048C>T c.1229C>T (p.Pro410Leu) | dbSNP gnomAD v2 gnomAD v4 |
X | g.40072338G>C | CA412741009 | BCOR | c.2997+11C>G (n.2997+11C>G) n.3048C>G c.1229C>G (p.Pro410Arg) | gnomAD v4 |
X | g.40072338G= | CA2425444189 | BCOR | c.2997+11C= (n.2997+11C=) n.3048C= c.1229C= (p.Pro410=) | |
X | g.40072338G>T | CA412741007 | BCOR | c.2997+11C>A (n.2997+11C>A) n.3048C>A c.1229C>A (p.Pro410His) | dbSNP gnomAD v2 gnomAD v4 |
X | g.40072339G>A | CA412741010 | BCOR | c.2997+10C>T (n.2997+10C>T) n.3047C>T c.1228C>T (p.Pro410Ser) | gnomAD v3 gnomAD v4 |
X | g.40072339G>C | CA327991388 | BCOR | c.2997+10C>G (n.2997+10C>G) n.3047C>G c.1228C>G (p.Pro410Ala) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.40072339G= | CA2425444190 | BCOR | c.2997+10C= (n.2997+10C=) n.3047C= c.1228C= (p.Pro410=) | |
X | g.40072339G>T | CA412741011 | BCOR | c.2997+10C>A (n.2997+10C>A) n.3047C>A c.1228C>A (p.Pro410Thr) | |
X | g.40072340G>A | CA10386724 | BCOR | c.2997+9C>T (n.2997+9C>T) n.3046C>T c.1227C>T (p.Pro409=) | dbSNP ExAC |
X | g.40072340G= | CA2425444191 | BCOR | c.2997+9C= (n.2997+9C=) n.3046C= c.1227C= (p.Pro409=) | |
X | g.40072340G>T | CA2550459870 | BCOR | c.2997+9C>A (n.2997+9C>A) n.3046C>A c.1227C>A (p.Pro409=) | |
X | g.40072341G>A | CA10386725 | BCOR | c.2997+8C>T (n.2997+8C>T) n.3045C>T c.1226C>T (p.Pro409Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.40072341G>C | CA412741012 | BCOR | c.2997+8C>G (n.2997+8C>G) n.3045C>G c.1226C>G (p.Pro409Arg) | |
X | g.40072341G= | CA2425444192 | BCOR | c.2997+8C= (n.2997+8C=) n.3045C= c.1226C= (p.Pro409=) | |
X | g.40072341G>T | CA412741013 | BCOR | c.2997+8C>A (n.2997+8C>A) n.3045C>A c.1226C>A (p.Pro409His) | dbSNP gnomAD v2 gnomAD v4 |
X | g.40072342G>A | CA412741014 | BCOR | c.2997+7C>T (n.2997+7C>T) n.3044C>T c.1225C>T (p.Pro409Ser) | gnomAD v4 |
X | g.40072342G>C | CA412741015 | BCOR | c.2997+7C>G (n.2997+7C>G) n.3044C>G c.1225C>G (p.Pro409Ala) | dbSNP gnomAD v2 gnomAD v4 |
X | g.40072342G= | CA2425444193 | BCOR | c.2997+7C= (n.2997+7C=) n.3044C= c.1225C= (p.Pro409=) | |
X | g.40072342G>T | CA412741016 | BCOR | c.2997+7C>A (n.2997+7C>A) n.3044C>A c.1225C>A (p.Pro409Thr) | |
X | g.40072343G>A | CA641363333 | BCOR | c.2997+6C>T (n.2997+6C>T) n.3043C>T c.1224C>T (p.Ser408=) | dbSNP gnomAD v2 gnomAD v4 |
X | g.40072343G>C | CA412741017 | BCOR | c.2997+6C>G (n.2997+6C>G) n.3043C>G c.1224C>G (p.Ser408Arg) | |
X | g.40072343G= | CA2425444194 | BCOR | c.2997+6C= (n.2997+6C=) n.3043C= c.1224C= (p.Ser408=) | |
X | g.40072343G>T | CA412741018 | BCOR | c.2997+6C>A (n.2997+6C>A) n.3043C>A c.1224C>A (p.Ser408Arg) | |
X | g.40072344C>A | CA412741019 | BCOR | c.2997+5G>T (n.2997+5G>T) n.3042G>T c.1223G>T (p.Ser408Ile) | |
X | g.40072344C>G | CA412741020 | BCOR | c.2997+5G>C (n.2997+5G>C) n.3042G>C c.1223G>C (p.Ser408Thr) | |
X | g.40072344C>T | CA412741021 | BCOR | c.2997+5G>A (n.2997+5G>A) n.3042G>A c.1223G>A (p.Ser408Asn) | dbSNP |
X | g.40072345T>A | CA412741022 | BCOR | c.2997+4A>T (n.2997+4A>T) n.3041A>T c.1222A>T (p.Ser408Cys) | |
X | g.40072345T>C | CA412741023 | BCOR | c.2997+4A>G (n.2997+4A>G) n.3041A>G c.1222A>G (p.Ser408Gly) | |
X | g.40072345T>G | CA412741024 | BCOR | c.2997+4A>C (n.2997+4A>C) n.3041A>C c.1222A>C (p.Ser408Arg) | |
X | g.40072346C>A | CA2693454671 | BCOR | c.2997+3G>T (n.2997+3G>T) n.3040G>T c.1221G>T (p.Val407=) | gnomAD v4 |
X | g.40072347A>C | CA412741027 | BCOR | c.2997+2T>G (n.2997+2T>G) n.3039T>G c.1220T>G (p.Val407Gly) | |
X | g.40072347A>G | CA412741025 | BCOR | c.2997+2T>C (n.2997+2T>C) n.3039T>C c.1220T>C (p.Val407Ala) | gnomAD v4 |
X | g.40072347A>T | CA412741026 | BCOR | c.2997+2T>A (n.2997+2T>A) n.3039T>A c.1220T>A (p.Val407Glu) | |
X | g.40072348C>A | CA412741028 | BCOR | c.2997+1G>T (n.2997+1G>T) n.3038G>T c.1219G>T (p.Val407Leu) | |
X | g.40072348C>G | CA412741029 | BCOR | c.2997+1G>C (n.2997+1G>C) n.3038G>C c.1219G>C (p.Val407Leu) | |
X | g.40072348C>T | CA412741030 | BCOR | c.2997+1G>A (n.2997+1G>A) n.3038G>A c.1219G>A (p.Val407Met) | dbSNP |
X | g.40072349C>A | CA412741031 | BCOR | c.2997G>T (p.Gln999His) n.3037G>T c.1218G>T (p.Gln406His) | |
X | g.40072349C>G | CA412741032 | BCOR | c.2997G>C (p.Gln999His) n.3037G>C c.1218G>C (p.Gln406His) | |
X | g.40072349C>T | CA516345132 | BCOR | c.2997G>A (p.Gln999=) n.3037G>A c.1218G>A (p.Gln406=) | gnomAD v4 |
X | g.40072350T>A | CA412741033 | BCOR | c.2996A>T (p.Gln999Leu) n.3036A>T c.1217A>T (p.Gln406Leu) | |
X | g.40072350T>C | CA412741034 | BCOR | c.2996A>G (p.Gln999Arg) n.3036A>G c.1217A>G (p.Gln406Arg) | gnomAD v4 |
X | g.40072350T>G | CA412741035 | BCOR | c.2996A>C (p.Gln999Pro) n.3036A>C c.1217A>C (p.Gln406Pro) | |
X | g.40072351G>A | CA412741036 | BCOR | c.2995C>T (p.Gln999Ter) n.3035C>T c.1216C>T (p.Gln406Ter) | dbSNP gnomAD v4 |
X | g.40072351G>C | CA412741037 | BCOR | c.2995C>G (p.Gln999Glu) n.3035C>G c.1216C>G (p.Gln406Glu) | |
X | g.40072351G>T | CA412741038 | BCOR | c.2995C>A (p.Gln999Lys) n.3035C>A c.1216C>A (p.Gln406Lys) | gnomAD v4 |
X | g.40072352C>A | CA412741040 | BCOR | c.2994G>T (p.Leu998Phe) n.3034G>T c.1215G>T (p.Leu405Phe) | |
X | g.40072352C>G | CA412741039 | BCOR | c.2994G>C (p.Leu998Phe) n.3034G>C c.1215G>C (p.Leu405Phe) | |
X | g.40072352C>T | CA516345134 | BCOR | c.2994G>A (p.Leu998=) n.3034G>A c.1215G>A (p.Leu405=) | |
X | g.40072353A>C | CA412741041 | BCOR | c.2993T>G (p.Leu998Trp) n.3033T>G c.1214T>G (p.Leu405Trp) | |
X | g.40072353A>G | CA412741042 | BCOR | c.2993T>C (p.Leu998Ser) n.3033T>C c.1214T>C (p.Leu405Ser) | |
X | g.40072353A>T | CA412741043 | BCOR | c.2993T>A (p.Leu998Ter) n.3033T>A c.1214T>A (p.Leu405Ter) | |
X | g.40072354A>C | CA412741044 | BCOR | c.2992T>G (p.Leu998Val) n.3032T>G c.1213T>G (p.Leu405Val) | |
X | g.40072354A>G | CA516345136 | BCOR | c.2992T>C (p.Leu998=) n.3032T>C c.1213T>C (p.Leu405=) | |
X | g.40072354A>T | CA412741045 | BCOR | c.2992T>A (p.Leu998Met) n.3032T>A c.1213T>A (p.Leu405Met) | |
X | g.40072355T>A | CA516345137 | BCOR | c.2991A>T (p.Ala997=) n.3031A>T c.1212A>T (p.Ala404=) | |
X | g.40072355T>C | CA10386726 | BCOR | c.2991A>G (p.Ala997=) n.3031A>G c.1212A>G (p.Ala404=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.40072355T>G | CA516345139 | BCOR | c.2991A>C (p.Ala997=) n.3031A>C c.1212A>C (p.Ala404=) | |
X | g.40072355T= | CA2425444195 | BCOR | c.2991A= (p.Ala997=) n.3031A= c.1212A= (p.Ala404=) | |
X | g.40072356G>A | CA412741046 | BCOR | c.2990C>T (p.Ala997Val) n.3030C>T c.1211C>T (p.Ala404Val) | |
X | g.40072356G>C | CA412741047 | BCOR | c.2990C>G (p.Ala997Gly) n.3030C>G c.1211C>G (p.Ala404Gly) | |
X | g.40072356G>T | CA412741048 | BCOR | c.2990C>A (p.Ala997Glu) n.3030C>A c.1211C>A (p.Ala404Glu) | |
X | g.40072357C>A | CA412741049 | BCOR | c.2989G>T (p.Ala997Ser) n.3029G>T c.1210G>T (p.Ala404Ser) | |
X | g.40072357C= | CA2425444196 | BCOR | c.2989G= (p.Ala997=) n.3029G= c.1210G= (p.Ala404=) | |
X | g.40072357C>G | CA412741050 | BCOR | c.2989G>C (p.Ala997Pro) n.3029G>C c.1210G>C (p.Ala404Pro) | |
X | g.40072357C>T | CA10386727 | BCOR | c.2989G>A (p.Ala997Thr) n.3029G>A c.1210G>A (p.Ala404Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.40072359del | CA915940569 | BCOR | c.2989del (p.Ala997HisfsTer24) c.2989del (p.Ala997HisfsTer6) n.3029del c.1210del (p.Ala404HisfsTer4) | |
X | g.40072358C>A | CA516345140 | BCOR | c.2988G>T (p.Arg996=) n.3028G>T c.1209G>T (p.Arg403=) | gnomAD v4 |
X | g.40072358C>G | CA516345141 | BCOR | c.2988G>C (p.Arg996=) n.3028G>C c.1209G>C (p.Arg403=) | |
X | g.40072358C>T | CA516345142 | BCOR | c.2988G>A (p.Arg996=) n.3028G>A c.1209G>A (p.Arg403=) | gnomAD v4 |
X | g.40072359C>A | CA412741053 | BCOR | c.2987G>T (p.Arg996Leu) n.3027G>T c.1208G>T (p.Arg403Leu) | |
X | g.40072359C>G | CA412741052 | BCOR | c.2987G>C (p.Arg996Pro) n.3027G>C c.1208G>C (p.Arg403Pro) | |
X | g.40072359C>T | CA412741051 | BCOR | c.2987G>A (p.Arg996Gln) n.3027G>A c.1208G>A (p.Arg403Gln) | |
X | g.40072360G>A | CA412741054 | BCOR | c.2986C>T (p.Arg996Trp) n.3026C>T c.1207C>T (p.Arg403Trp) | dbSNP gnomAD v4 |
X | g.40072360G>C | CA412741055 | BCOR | c.2986C>G (p.Arg996Gly) n.3026C>G c.1207C>G (p.Arg403Gly) | |
X | g.40072360G>T | CA516345145 | BCOR | c.2986C>A (p.Arg996=) n.3026C>A c.1207C>A (p.Arg403=) | |
X | g.40072361T>A | CA412741056 | BCOR | c.2985A>T (p.Gln995His) n.3025A>T c.1206A>T (p.Gln402His) | |
X | g.40072361T>C | CA10386728 | BCOR | c.2985A>G (p.Gln995=) n.3025A>G c.1206A>G (p.Gln402=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.40072361T>G | CA412741057 | BCOR | c.2985A>C (p.Gln995His) n.3025A>C c.1206A>C (p.Gln402His) | dbSNP |
X | g.40072361T= | CA2425444197 | BCOR | c.2985A= (p.Gln995=) n.3025A= c.1206A= (p.Gln402=) | |
X | g.40072362T>A | CA412741058 | BCOR | c.2984A>T (p.Gln995Leu) n.3024A>T c.1205A>T (p.Gln402Leu) | |
X | g.40072362T>C | CA412741059 | BCOR | c.2984A>G (p.Gln995Arg) n.3024A>G c.1205A>G (p.Gln402Arg) | |
X | g.40072362T>G | CA412741060 | BCOR | c.2984A>C (p.Gln995Pro) n.3024A>C c.1205A>C (p.Gln402Pro) | |
X | g.40072363del | CA2579585695 | BCOR | c.2983del (p.Gln995AsnfsTer26) c.2983del (p.Gln995AsnfsTer8) n.3023del c.1204del (p.Gln402AsnfsTer6) | |
X | g.40072363G>A | CA412741061 | BCOR | c.2983C>T (p.Gln995Ter) n.3023C>T c.1204C>T (p.Gln402Ter) | ClinVar |
X | g.40072363G>C | CA412741062 | BCOR | c.2983C>G (p.Gln995Glu) n.3023C>G c.1204C>G (p.Gln402Glu) | COSMIC COSMIC |
X | g.40072363G>T | CA412741063 | BCOR | c.2983C>A (p.Gln995Lys) n.3023C>A c.1204C>A (p.Gln402Lys) | gnomAD v4 |
X | g.40072364C>A | CA412741064 | BCOR | c.2982G>T (p.Glu994Asp) n.3022G>T c.1203G>T (p.Glu401Asp) | gnomAD v4 |
X | g.40072364C>G | CA412741065 | BCOR | c.2982G>C (p.Glu994Asp) n.3022G>C c.1203G>C (p.Glu401Asp) | |
X | g.40072364C>T | CA516345150 | BCOR | c.2982G>A (p.Glu994=) n.3022G>A c.1203G>A (p.Glu401=) | |
X | g.40072365T>A | CA412741067 | BCOR | c.2981A>T (p.Glu994Val) n.3021A>T c.1202A>T (p.Glu401Val) | |
X | g.40072365T>C | CA412741068 | BCOR | c.2981A>G (p.Glu994Gly) n.3021A>G c.1202A>G (p.Glu401Gly) | |
X | g.40072365T>G | CA412741066 | BCOR | c.2981A>C (p.Glu994Ala) n.3021A>C c.1202A>C (p.Glu401Ala) | |
X | g.40072366C>A | CA412741071 | BCOR | c.2980G>T (p.Glu994Ter) n.3020G>T c.1201G>T (p.Glu401Ter) | |
X | g.40072366C>G | CA412741069 | BCOR | c.2980G>C (p.Glu994Gln) n.3020G>C c.1201G>C (p.Glu401Gln) | |
X | g.40072366C>T | CA412741070 | BCOR | c.2980G>A (p.Glu994Lys) n.3020G>A c.1201G>A (p.Glu401Lys) | |
X | g.40072367C>A | CA516345158 | BCOR | c.2979G>T (p.Arg993=) n.3019G>T c.1200G>T (p.Arg400=) | dbSNP gnomAD v2 gnomAD v4 |
X | g.40072367C= | CA2425444198 | BCOR | c.2979G= (p.Arg993=) n.3019G= c.1200G= (p.Arg400=) | |
X | g.40072367C>G | CA516345159 | BCOR | c.2979G>C (p.Arg993=) n.3019G>C c.1200G>C (p.Arg400=) | |
X | g.40072367C>T | CA516345160 | BCOR | c.2979G>A (p.Arg993=) n.3019G>A c.1200G>A (p.Arg400=) | dbSNP |
X | g.40072368C>A | CA10386729 | BCOR | c.2978G>T (p.Arg993Leu) n.3018G>T c.1199G>T (p.Arg400Leu) | dbSNP ExAC gnomAD v2 |
X | g.40072368C= | CA2425444199 | BCOR | c.2978G= (p.Arg993=) n.3018G= c.1199G= (p.Arg400=) | |
X | g.40072368C>G | CA412741072 | BCOR | c.2978G>C (p.Arg993Pro) n.3018G>C c.1199G>C (p.Arg400Pro) | dbSNP |
X | g.40072368C>T | CA16608918 | BCOR | c.2978G>A (p.Arg993Gln) n.3018G>A c.1199G>A (p.Arg400Gln) | ClinVar dbSNP gnomAD v4 |
X | g.40072369G>A | CA412741073 | BCOR | c.2977C>T (p.Arg993Trp) n.3017C>T c.1198C>T (p.Arg400Trp) | dbSNP gnomAD v4 |
X | g.40072369G>C | CA412741074 | BCOR | c.2977C>G (p.Arg993Gly) n.3017C>G c.1198C>G (p.Arg400Gly) | dbSNP |
X | g.40072369G>T | CA516345162 | BCOR | c.2977C>A (p.Arg993=) n.3017C>A c.1198C>A (p.Arg400=) | |
X | g.40072370G>A | CA516345164 | BCOR | c.2976C>T (p.Ser992=) n.3016C>T c.1197C>T (p.Ser399=) | |
X | g.40072370G>C | CA412741075 | BCOR | c.2976C>G (p.Ser992Arg) n.3016C>G c.1197C>G (p.Ser399Arg) | |
X | g.40072370G>T | CA412741076 | BCOR | c.2976C>A (p.Ser992Arg) n.3016C>A c.1197C>A (p.Ser399Arg) | |
X | g.40072371C>A | CA412741077 | BCOR | c.2975G>T (p.Ser992Ile) n.3015G>T c.1196G>T (p.Ser399Ile) | |
X | g.40072371C>G | CA412741078 | BCOR | c.2975G>C (p.Ser992Thr) n.3015G>C c.1196G>C (p.Ser399Thr) | |
X | g.40072371C>T | CA412741079 | BCOR | c.2975G>A (p.Ser992Asn) n.3015G>A c.1196G>A (p.Ser399Asn) | |
X | g.40072372T>A | CA412741082 | BCOR | c.2974A>T (p.Ser992Cys) n.3014A>T c.1195A>T (p.Ser399Cys) | |
X | g.40072372T>C | CA412741080 | BCOR | c.2974A>G (p.Ser992Gly) n.3014A>G c.1195A>G (p.Ser399Gly) | |
X | g.40072372T>G | CA412741081 | BCOR | c.2974A>C (p.Ser992Arg) n.3014A>C c.1195A>C (p.Ser399Arg) | |
X | g.40072373G>A | CA516345167 | BCOR | c.2973C>T (p.Leu991=) n.3013C>T c.1194C>T (p.Leu398=) | |
X | g.40072373G>C | CA516345168 | BCOR | c.2973C>G (p.Leu991=) n.3013C>G c.1194C>G (p.Leu398=) | |
X | g.40072373G>T | CA516345169 | BCOR | c.2973C>A (p.Leu991=) n.3013C>A c.1194C>A (p.Leu398=) | |
X | g.40072374A>C | CA412741083 | BCOR | c.2972T>G (p.Leu991Arg) n.3012T>G c.1193T>G (p.Leu398Arg) | |
X | g.40072374A>G | CA412741084 | BCOR | c.2972T>C (p.Leu991Pro) n.3012T>C c.1193T>C (p.Leu398Pro) | |
X | g.40072374A>T | CA412741085 | BCOR | c.2972T>A (p.Leu991His) n.3012T>A c.1193T>A (p.Leu398His) | |
X | g.40072375G>A | CA412741086 | BCOR | c.2971C>T (p.Leu991Phe) n.3011C>T c.1192C>T (p.Leu398Phe) | |
X | g.40072375G>C | CA412741087 | BCOR | c.2971C>G (p.Leu991Val) n.3011C>G c.1192C>G (p.Leu398Val) | dbSNP |
X | g.40072375G>T | CA412741088 | BCOR | c.2971C>A (p.Leu991Ile) n.3011C>A c.1192C>A (p.Leu398Ile) | |
X | g.40072376C>A | CA412741089 | BCOR | c.2970G>T (p.Gln990His) n.3010G>T c.1191G>T (p.Gln397His) | |
X | g.40072376C>G | CA412741090 | BCOR | c.2970G>C (p.Gln990His) n.3010G>C c.1191G>C (p.Gln397His) | |
X | g.40072376C>T | CA516345174 | BCOR | c.2970G>A (p.Gln990=) n.3010G>A c.1191G>A (p.Gln397=) | dbSNP |
X | g.40072377T>A | CA412741091 | BCOR | c.2969A>T (p.Gln990Leu) n.3009A>T c.1190A>T (p.Gln397Leu) | |
X | g.40072377T>C | CA412741092 | BCOR | c.2969A>G (p.Gln990Arg) n.3009A>G c.1190A>G (p.Gln397Arg) | |
X | g.40072377T>G | CA412741093 | BCOR | c.2969A>C (p.Gln990Pro) n.3009A>C c.1190A>C (p.Gln397Pro) | |
X | g.40072378G>A | CA412741095 | BCOR | c.2968C>T (p.Gln990Ter) n.3008C>T c.1189C>T (p.Gln397Ter) | |
X | g.40072378G>C | CA412741096 | BCOR | c.2968C>G (p.Gln990Glu) n.3008C>G c.1189C>G (p.Gln397Glu) | |
X | g.40072378G>T | CA412741094 | BCOR | c.2968C>A (p.Gln990Lys) n.3008C>A c.1189C>A (p.Gln397Lys) | |
X | g.40072379A>C | CA412741097 | BCOR | c.2967T>G (p.Ser989Arg) n.3007T>G c.1188T>G (p.Ser396Arg) | |
X | g.40072379A>G | CA516345178 | BCOR | c.2967T>C (p.Ser989=) n.3007T>C c.1188T>C (p.Ser396=) | |
X | g.40072379A>T | CA412741098 | BCOR | c.2967T>A (p.Ser989Arg) n.3007T>A c.1188T>A (p.Ser396Arg) | dbSNP |
X | g.40072380C>A | CA412741099 | BCOR | c.2966G>T (p.Ser989Ile) n.3006G>T c.1187G>T (p.Ser396Ile) | |
X | g.40072380C>G | CA412741100 | BCOR | c.2966G>C (p.Ser989Thr) n.3006G>C c.1187G>C (p.Ser396Thr) | |
X | g.40072380C>T | CA412741101 | BCOR | c.2966G>A (p.Ser989Asn) n.3006G>A c.1187G>A (p.Ser396Asn) | |
X | g.40072381T>A | CA412741102 | BCOR | c.2965A>T (p.Ser989Cys) n.3005A>T c.1186A>T (p.Ser396Cys) | |
X | g.40072381T>C | CA412741103 | BCOR | c.2965A>G (p.Ser989Gly) n.3005A>G c.1186A>G (p.Ser396Gly) | |
X | g.40072381T>G | CA412741104 | BCOR | c.2965A>C (p.Ser989Arg) n.3005A>C c.1186A>C (p.Ser396Arg) | |
X | g.40072382G>A | CA516345181 | BCOR | c.2964C>T (p.Ser988=) n.3004C>T c.1185C>T (p.Ser395=) | |
X | g.40072382G>C | CA516345183 | BCOR | c.2964C>G (p.Ser988=) n.3004C>G c.1185C>G (p.Ser395=) | dbSNP |
X | g.40072382G>T | CA516345185 | BCOR | c.2964C>A (p.Ser988=) n.3004C>A c.1185C>A (p.Ser395=) | gnomAD v4 |
X | g.40072383G>A | CA412741107 | BCOR | c.2963C>T (p.Ser988Phe) n.3003C>T c.1184C>T (p.Ser395Phe) | |
X | g.40072383G>C | CA412741109 | BCOR | c.2963C>G (p.Ser988Cys) n.3003C>G c.1184C>G (p.Ser395Cys) | dbSNP |
X | g.40072383G>T | CA412741111 | BCOR | c.2963C>A (p.Ser988Tyr) n.3003C>A c.1184C>A (p.Ser395Tyr) | |
X | g.40072384A>C | CA412741112 | BCOR | c.2962T>G (p.Ser988Ala) n.3002T>G c.1183T>G (p.Ser395Ala) | |
X | g.40072384A>G | CA412741114 | BCOR | c.2962T>C (p.Ser988Pro) n.3002T>C c.1183T>C (p.Ser395Pro) | |
X | g.40072384A>T | CA412741116 | BCOR | c.2962T>A (p.Ser988Thr) n.3002T>A c.1183T>A (p.Ser395Thr) | |
X | g.40072385A>C | CA412741120 | BCOR | c.2961T>G (p.Asp987Glu) n.3001T>G c.1182T>G (p.Asp394Glu) | |
X | g.40072385A>G | CA516345187 | BCOR | c.2961T>C (p.Asp987=) n.3001T>C c.1182T>C (p.Asp394=) | |
X | g.40072385A>T | CA412741122 | BCOR | c.2961T>A (p.Asp987Glu) n.3001T>A c.1182T>A (p.Asp394Glu) | |
X | g.40072386T>A | CA412741124 | BCOR | c.2960A>T (p.Asp987Val) n.3000A>T c.1181A>T (p.Asp394Val) | |
X | g.40072386T>C | CA412741126 | BCOR | c.2960A>G (p.Asp987Gly) n.3000A>G c.1181A>G (p.Asp394Gly) | |
X | g.40072386T>G | CA412741129 | BCOR | c.2960A>C (p.Asp987Ala) n.3000A>C c.1181A>C (p.Asp394Ala) | |
X | g.40072387C>A | CA412741131 | BCOR | c.2959G>T (p.Asp987Tyr) n.2999G>T c.1180G>T (p.Asp394Tyr) | |
X | g.40072387C>G | CA412741133 | BCOR | c.2959G>C (p.Asp987His) n.2999G>C c.1180G>C (p.Asp394His) | |
X | g.40072387C>T | CA412741136 | BCOR | c.2959G>A (p.Asp987Asn) n.2999G>A c.1180G>A (p.Asp394Asn) | |
X | g.40072388T>A | CA516345190 | BCOR | c.2958A>T (p.Ala986=) n.2998A>T c.1179A>T (p.Ala393=) | |
X | g.40072388T>C | CA516345191 | BCOR | c.2958A>G (p.Ala986=) n.2998A>G c.1179A>G (p.Ala393=) | gnomAD v4 |
X | g.40072388T>G | CA516345193 | BCOR | c.2958A>C (p.Ala986=) n.2998A>C c.1179A>C (p.Ala393=) | |
X | g.40072389G>A | CA412741140 | BCOR | c.2957C>T (p.Ala986Val) n.2997C>T c.1178C>T (p.Ala393Val) | dbSNP |
X | g.40072389G>C | CA412741141 | BCOR | c.2957C>G (p.Ala986Gly) n.2997C>G c.1178C>G (p.Ala393Gly) | |
X | g.40072389G>T | CA412741144 | BCOR | c.2957C>A (p.Ala986Glu) n.2997C>A c.1178C>A (p.Ala393Glu) | |
X | g.40072390C>A | CA412741148 | BCOR | c.2956G>T (p.Ala986Ser) n.2996G>T c.1177G>T (p.Ala393Ser) | |
X | g.40072390C>G | CA412741150 | BCOR | c.2956G>C (p.Ala986Pro) n.2996G>C c.1177G>C (p.Ala393Pro) | |
X | g.40072390C>T | CA412741152 | BCOR | c.2956G>A (p.Ala986Thr) n.2996G>A c.1177G>A (p.Ala393Thr) | dbSNP |
X | g.40072391A>C | CA412741154 | BCOR | c.2955T>G (p.Tyr985Ter) n.2995T>G c.1176T>G (p.Tyr392Ter) | |
X | g.40072391A>G | CA516345198 | BCOR | c.2955T>C (p.Tyr985=) n.2995T>C c.1176T>C (p.Tyr392=) | |
X | g.40072391A>T | CA412741155 | BCOR | c.2955T>A (p.Tyr985Ter) n.2995T>A c.1176T>A (p.Tyr392Ter) | dbSNP |
X | g.40072392T>A | CA157293 | BCOR | c.2954A>T (p.Tyr985Phe) n.2994A>T c.1175A>T (p.Tyr392Phe) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.40072392T>C | CA10386730 | BCOR | c.2954A>G (p.Tyr985Cys) n.2994A>G c.1175A>G (p.Tyr392Cys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.40072392T>G | CA412741158 | BCOR | c.2954A>C (p.Tyr985Ser) n.2994A>C c.1175A>C (p.Tyr392Ser) | |
X | g.40072392T= | CA2425444200 | BCOR | c.2954A= (p.Tyr985=) n.2994A= c.1175A= (p.Tyr392=) |