10 | g.71834398G>A | CA377155827 | PSAP | c.148C>T (p.Gln50Ter)
| ClinVar |
10 | g.71834398G>C | CA377155828 | PSAP | c.148C>G (p.Gln50Glu)
| |
10 | g.71834398G>T | CA377155829 | PSAP | c.148C>A (p.Gln50Lys)
| |
10 | g.71834399C>A | CA470061827 | PSAP | c.147G>T (p.Leu49=)
| |
10 | g.71834399C= | CA1918891061 | PSAP | c.147G= (p.Leu49=)
| |
10 | g.71834399C>G | CA470061828 | PSAP | c.147G>C (p.Leu49=)
| |
10 | g.71834399C>T | CA5547885 | PSAP | c.147G>A (p.Leu49=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.71834400A>C | CA377155843 | PSAP | c.146T>G (p.Leu49Arg)
| |
10 | g.71834400A>G | CA377155834 | PSAP | c.146T>C (p.Leu49Pro)
| |
10 | g.71834400A>T | CA377155831 | PSAP | c.146T>A (p.Leu49Gln)
| |
10 | g.71834401G>A | CA470061829 | PSAP | c.145C>T (p.Leu49=)
| ClinVar dbSNP COSMIC COSMIC |
10 | g.71834401G>C | CA377155845 | PSAP | c.145C>G (p.Leu49Val)
| |
10 | g.71834401G= | CA1918891064 | PSAP | c.145C= (p.Leu49=)
| |
10 | g.71834401G>T | CA377155847 | PSAP | c.145C>A (p.Leu49Met)
| |
10 | g.71834402G>A | CA470061830 | PSAP | c.144C>T (p.Cys48=)
| gnomAD v4 |
10 | g.71834402G>C | CA377155857 | PSAP | c.144C>G (p.Cys48Trp)
| |
10 | g.71834402G>T | CA377155860 | PSAP | c.144C>A (p.Cys48Ter)
| |
10 | g.71834403C>A | CA377155862 | PSAP | c.143G>T (p.Cys48Phe)
| |
10 | g.71834403C>G | CA377155864 | PSAP | c.143G>C (p.Cys48Ser)
| |
10 | g.71834403C>T | CA377155872 | PSAP | c.143G>A (p.Cys48Tyr)
| |
10 | g.71834404A>C | CA377155875 | PSAP | c.142T>G (p.Cys48Gly)
| |
10 | g.71834404A>G | CA377155877 | PSAP | c.142T>C (p.Cys48Arg)
| |
10 | g.71834404A>T | CA377155878 | PSAP | c.142T>A (p.Cys48Ser)
| |
10 | g.71834405G>A | CA5547886 | PSAP | c.141C>T (p.His47=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.71834405G>C | CA377155887 | PSAP | c.141C>G (p.His47Gln)
| |
10 | g.71834405G= | CA1918891067 | PSAP | c.141C= (p.His47=)
| |
10 | g.71834405G>T | CA377155890 | PSAP | c.141C>A (p.His47Gln)
| |
10 | g.71834406T>A | CA377155894 | PSAP | c.140A>T (p.His47Leu)
| |
10 | g.71834406T>C | CA377155895 | PSAP | c.140A>G (p.His47Arg)
| gnomAD v4 |
10 | g.71834406T>G | CA377155893 | PSAP | c.140A>C (p.His47Pro)
| |
10 | g.71834406T= | CA1918891070 | PSAP | c.140A= (p.His47=)
| |
10 | g.71834407G>A | CA5547887 | PSAP | c.139C>T (p.His47Tyr)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.71834407G>C | CA377155896 | PSAP | c.139C>G (p.His47Asp)
| |
10 | g.71834407G= | CA1918891072 | PSAP | c.139C= (p.His47=)
| |
10 | g.71834407G>T | CA377155897 | PSAP | c.139C>A (p.His47Asn)
| |
10 | g.71834407_71834408dup | CA594311245 | PSAP | c.138_139dup (p.His47ArgfsTer13)
| dbSNP gnomAD v2 |
10 | g.71834408C>A | CA5547888 | PSAP | c.138G>T (p.Lys46Asn)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.71834408C= | CA1918891073 | PSAP | c.138G= (p.Lys46=)
| |
10 | g.71834408C>G | CA377155899 | PSAP | c.138G>C (p.Lys46Asn)
| |
10 | g.71834408C>T | CA470061831 | PSAP | c.138G>A (p.Lys46=)
| |
10 | g.71834408_71834410delinsAAG | CA2573145297 | PSAP | c.136_138delinsCTT (p.Lys46Leu)
| ClinVar |
10 | g.71834409T>A | CA377155902 | PSAP | c.137A>T (p.Lys46Met)
| dbSNP gnomAD v2 gnomAD v4 |
10 | g.71834409T>C | CA377155904 | PSAP | c.137A>G (p.Lys46Arg)
| |
10 | g.71834409T>G | CA377155907 | PSAP | c.137A>C (p.Lys46Thr)
| |
10 | g.71834409T= | CA1918891075 | PSAP | c.137A= (p.Lys46=)
| |
10 | g.71834410T>A | CA377155909 | PSAP | c.136A>T (p.Lys46Ter)
| |
10 | g.71834410T>C | CA377155911 | PSAP | c.136A>G (p.Lys46Glu)
| |
10 | g.71834410T>G | CA377155914 | PSAP | c.136A>C (p.Lys46Gln)
| dbSNP gnomAD v2 gnomAD v4 |
10 | g.71834410T= | CA1918891076 | PSAP | c.136A= (p.Lys46=)
| |
10 | g.71834411C>A | CA470061832 | PSAP | c.135G>T (p.Val45=)
| |
10 | g.71834411C>G | CA470061834 | PSAP | c.135G>C (p.Val45=)
| |
10 | g.71834411C>T | CA470061833 | PSAP | c.135G>A (p.Val45=)
| |
10 | g.71834412A>C | CA377155919 | PSAP | c.134T>G (p.Val45Gly)
| |
10 | g.71834412A>G | CA377155932 | PSAP | c.134T>C (p.Val45Ala)
| gnomAD v4 |
10 | g.71834412A>T | CA377155936 | PSAP | c.134T>A (p.Val45Glu)
| |
10 | g.71834413C>A | CA5547889 | PSAP | c.133G>T (p.Val45Leu)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.71834413C= | CA1918891079 | PSAP | c.133G= (p.Val45=)
| |
10 | g.71834413C>G | CA5547890 | PSAP | c.133G>C (p.Val45Leu)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.71834413C>T | CA377155942 | PSAP | c.133G>A (p.Val45Met)
| |
10 | g.71834414T>A | CA470061835 | PSAP | c.132A>T (p.Ala44=)
| |
10 | g.71834414T>C | CA470061836 | PSAP | c.132A>G (p.Ala44=)
| ClinVar dbSNP gnomAD v4 |
10 | g.71834414T>G | CA470061837 | PSAP | c.132A>C (p.Ala44=)
| |
10 | g.71834415G>A | CA5547891 | PSAP | c.131C>T (p.Ala44Val)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.71834415G>C | CA377155943 | PSAP | c.131C>G (p.Ala44Gly)
| |
10 | g.71834415G= | CA1918891080 | PSAP | c.131C= (p.Ala44=)
| |
10 | g.71834415G>T | CA377155944 | PSAP | c.131C>A (p.Ala44Glu)
| |
10 | g.71834416C>A | CA377155945 | PSAP | c.130G>T (p.Ala44Ser)
| |
10 | g.71834416C>G | CA377155947 | PSAP | c.130G>C (p.Ala44Pro)
| |
10 | g.71834416C>T | CA377155948 | PSAP | c.130G>A (p.Ala44Thr)
| |
10 | g.71834417C>A | CA470061838 | PSAP | c.129G>T (p.Gly43=)
| |
10 | g.71834417C>G | CA470061839 | PSAP | c.129G>C (p.Gly43=)
| |
10 | g.71834417C>T | CA470061840 | PSAP | c.129G>A (p.Gly43=)
| |
10 | g.71834418C>A | CA377155950 | PSAP | c.128G>T (p.Gly43Val)
| |
10 | g.71834418C= | CA1918891083 | PSAP | c.128G= (p.Gly43=)
| |
10 | g.71834418C>G | CA377155952 | PSAP | c.128G>C (p.Gly43Ala)
| |
10 | g.71834418C>T | CA5547892 | PSAP | c.128G>A (p.Gly43Glu)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.71834419C>A | CA377155961 | PSAP | c.127G>T (p.Gly43Trp)
| |
10 | g.71834419C= | CA1918891085 | PSAP | c.127G= (p.Gly43=)
| |
10 | g.71834419C>G | CA5547894 | PSAP | c.127G>C (p.Gly43Arg)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.71834419C>T | CA5547893 | PSAP | c.127G>A (p.Gly43Arg)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.71834420G>A | CA5547895 | PSAP | c.126C>T (p.Cys42=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
10 | g.71834420G>C | CA377155966 | PSAP | c.126C>G (p.Cys42Trp)
| |
10 | g.71834420G= | CA1918891089 | PSAP | c.126C= (p.Cys42=)
| |
10 | g.71834420G>T | CA377155968 | PSAP | c.126C>A (p.Cys42Ter)
| |
10 | g.71834421C>A | CA377155976 | PSAP | c.125G>T (p.Cys42Phe)
| |
10 | g.71834421C= | CA1918891091 | PSAP | c.125G= (p.Cys42=)
| |
10 | g.71834421C>G | CA377155975 | PSAP | c.125G>C (p.Cys42Ser)
| |
10 | g.71834421C>T | CA377155972 | PSAP | c.125G>A (p.Cys42Tyr)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.71834422A>C | CA377155994 | PSAP | c.124T>G (p.Cys42Gly)
| |
10 | g.71834422A>G | CA377155979 | PSAP | c.124T>C (p.Cys42Arg)
| |
10 | g.71834422A>T | CA377155982 | PSAP | c.124T>A (p.Cys42Ser)
| |
10 | g.71834423G>A | CA470061841 | PSAP | c.123C>T (p.Asp41=)
| |
10 | g.71834423G>C | CA377155997 | PSAP | c.123C>G (p.Asp41Glu)
| |
10 | g.71834423G>T | CA377155998 | PSAP | c.123C>A (p.Asp41Glu)
| |
10 | g.71834424T>A | CA377156001 | PSAP | c.122A>T (p.Asp41Val)
| |
10 | g.71834424T>C | CA377156003 | PSAP | c.122A>G (p.Asp41Gly)
| |
10 | g.71834424T>G | CA377156009 | PSAP | c.122A>C (p.Asp41Ala)
| |
10 | g.71834425C>A | CA5547896 | PSAP | c.121G>T (p.Asp41Tyr)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.71834425C= | CA1918891093 | PSAP | c.121G= (p.Asp41=)
| |
10 | g.71834425C>G | CA377156017 | PSAP | c.121G>C (p.Asp41His)
| dbSNP gnomAD v4 |
10 | g.71834425C>T | CA209471919 | PSAP | c.121G>A (p.Asp41Asn)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
10 | g.71834426G>A | CA5547897 | PSAP | c.120C>T (p.Ser40=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.71834426G>C | CA470061843 | PSAP | c.120C>G (p.Ser40=)
| |
10 | g.71834426G= | CA1918891095 | PSAP | c.120C= (p.Ser40=)
| |
10 | g.71834426G>T | CA470061842 | PSAP | c.120C>A (p.Ser40=)
| |
10 | g.71834427G>A | CA377156021 | PSAP | c.119C>T (p.Ser40Phe)
| |
10 | g.71834427G>C | CA377156023 | PSAP | c.119C>G (p.Ser40Cys)
| |
10 | g.71834427G= | CA1918891097 | PSAP | c.119C= (p.Ser40=)
| |
10 | g.71834427G>T | CA5547898 | PSAP | c.119C>A (p.Ser40Tyr)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.71834428A>C | CA377156028 | PSAP | c.118T>G (p.Ser40Ala)
| |
10 | g.71834428A>G | CA377156036 | PSAP | c.118T>C (p.Ser40Pro)
| |
10 | g.71834428A>T | CA377156034 | PSAP | c.118T>A (p.Ser40Thr)
| |
10 | g.71834429C>A | CA470061844 | PSAP | c.117G>T (p.Ala39=)
| |
10 | g.71834429C= | CA1918891099 | PSAP | c.117G= (p.Ala39=)
| |
10 | g.71834429C>G | CA470061845 | PSAP | c.117G>C (p.Ala39=)
| |
10 | g.71834429C>T | CA5547899 | PSAP | c.117G>A (p.Ala39=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
10 | g.71834430G>A | CA209471940 | PSAP | c.116C>T (p.Ala39Val)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.71834430G>C | CA377156038 | PSAP | c.116C>G (p.Ala39Gly)
| |
10 | g.71834430G= | CA1918891101 | PSAP | c.116C= (p.Ala39=)
| |
10 | g.71834430G>T | CA377156039 | PSAP | c.116C>A (p.Ala39Glu)
| |
10 | g.71834431C>A | CA377156040 | PSAP | c.115G>T (p.Ala39Ser)
| dbSNP gnomAD v4 |
10 | g.71834431C= | CA1918891103 | PSAP | c.115G= (p.Ala39=)
| |
10 | g.71834431C>G | CA377156042 | PSAP | c.115G>C (p.Ala39Pro)
| |
10 | g.71834431C>T | CA377156044 | PSAP | c.115G>A (p.Ala39Thr)
| |
10 | g.71834432C>A | CA470061846 | PSAP | c.114G>T (p.Thr38=)
| gnomAD v4 |
10 | g.71834432C= | CA1918891105 | PSAP | c.114G= (p.Thr38=)
| |
10 | g.71834432C>G | CA470061848 | PSAP | c.114G>C (p.Thr38=)
| ClinVar dbSNP |
10 | g.71834432C>T | CA5547900 | PSAP | c.114G>A (p.Thr38=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.71834433G>A | CA5547901 | PSAP | c.113C>T (p.Thr38Met)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.71834433G>C | CA377156046 | PSAP | c.113C>G (p.Thr38Arg)
| |
10 | g.71834433G= | CA1918891107 | PSAP | c.113C= (p.Thr38=)
| |
10 | g.71834433G>T | CA377156047 | PSAP | c.113C>A (p.Thr38Lys)
| |
10 | g.71834434T>A | CA5547902 | PSAP | c.112A>T (p.Thr38Ser)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.71834434T>C | CA5547903 | PSAP | c.112A>G (p.Thr38Ala)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.71834434T>G | CA377156049 | PSAP | c.112A>C (p.Thr38Pro)
| |
10 | g.71834434T= | CA1918891109 | PSAP | c.112A= (p.Thr38=)
| |
10 | g.71834435C>A | CA377156055 | PSAP | c.111G>T (p.Lys37Asn)
| |
10 | g.71834435C>G | CA377156058 | PSAP | c.111G>C (p.Lys37Asn)
| |
10 | g.71834435C>T | CA470061851 | PSAP | c.111G>A (p.Lys37=)
| |
10 | g.71834436T>A | CA377156063 | PSAP | c.110A>T (p.Lys37Met)
| |
10 | g.71834436T>C | CA377156064 | PSAP | c.110A>G (p.Lys37Arg)
| dbSNP gnomAD v4 |
10 | g.71834436T>G | CA377156065 | PSAP | c.110A>C (p.Lys37Thr)
| |
10 | g.71834436T= | CA1918891112 | PSAP | c.110A= (p.Lys37=)
| |
10 | g.71834437T>A | CA377156066 | PSAP | c.109A>T (p.Lys37Ter)
| |
10 | g.71834437T>C | CA377156067 | PSAP | c.109A>G (p.Lys37Glu)
| |
10 | g.71834437T>G | CA377156068 | PSAP | c.109A>C (p.Lys37Gln)
| |
10 | g.71834438C>A | CA470061853 | PSAP | c.108G>T (p.Val36=)
| |
10 | g.71834438C>G | CA470061854 | PSAP | c.108G>C (p.Val36=)
| |
10 | g.71834438C>T | CA470061855 | PSAP | c.108G>A (p.Val36=)
| |
10 | g.71834439A>C | CA377156069 | PSAP | c.107T>G (p.Val36Gly)
| |
10 | g.71834439A>G | CA377156070 | PSAP | c.107T>C (p.Val36Ala)
| |
10 | g.71834439A>T | CA377156072 | PSAP | c.107T>A (p.Val36Glu)
| |
10 | g.71834440C>A | CA377156076 | PSAP | c.106G>T (p.Val36Leu)
| |
10 | g.71834440C= | CA1918891114 | PSAP | c.106G= (p.Val36=)
| |
10 | g.71834440C>G | CA377156082 | PSAP | c.106G>C (p.Val36Leu)
| |
10 | g.71834440C>T | CA377156087 | PSAP | c.106G>A (p.Val36Met)
| dbSNP gnomAD v2 gnomAD v4 |
10 | g.71834441A= | CA1918891116 | PSAP | c.105T= (p.Asn35=)
| |
10 | g.71834441A>C | CA377156089 | PSAP | c.105T>G (p.Asn35Lys)
| |
10 | g.71834441A>G | CA470061856 | PSAP | c.105T>C (p.Asn35=)
| |
10 | g.71834441A>T | CA5547904 | PSAP | c.105T>A (p.Asn35Lys)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.71834442T>A | CA377156094 | PSAP | c.104A>T (p.Asn35Ile)
| |
10 | g.71834442T>C | CA209471981 | PSAP | c.104A>G (p.Asn35Ser)
| dbSNP |
10 | g.71834442T>G | CA377156099 | PSAP | c.104A>C (p.Asn35Thr)
| |
10 | g.71834442T= | CA1918891118 | PSAP | c.104A= (p.Asn35=)
| |
10 | g.71834443T>A | CA377156101 | PSAP | c.103A>T (p.Asn35Tyr)
| |
10 | g.71834443T>C | CA377156103 | PSAP | c.103A>G (p.Asn35Asp)
| |
10 | g.71834443T>G | CA377156104 | PSAP | c.103A>C (p.Asn35His)
| |
10 | g.71834444C>A | CA377156105 | PSAP | c.102G>T (p.Gln34His)
| |
10 | g.71834444C>G | CA377156106 | PSAP | c.102G>C (p.Gln34His)
| |
10 | g.71834444C>T | CA470061858 | PSAP | c.102G>A (p.Gln34=)
| |
10 | g.71834445T>A | CA377156107 | PSAP | c.101A>T (p.Gln34Leu)
| |
10 | g.71834445T>C | CA377156113 | PSAP | c.101A>G (p.Gln34Arg)
| |
10 | g.71834445T>G | CA377156115 | PSAP | c.101A>C (p.Gln34Pro)
| |
10 | g.71834446G>A | CA377156119 | PSAP | c.100C>T (p.Gln34Ter)
| |
10 | g.71834446G>C | CA377156122 | PSAP | c.100C>G (p.Gln34Glu)
| |
10 | g.71834446G>T | CA377156118 | PSAP | c.100C>A (p.Gln34Lys)
| |
10 | g.71834447del | CA2580081975 | PSAP | c.100del (p.Gln34ArgfsTer3)
| ClinVar |
10 | g.71834447G>A | CA470061859 | PSAP | c.99C>T (p.Cys33=)
| ClinVar gnomAD v4 |
10 | g.71834447G>C | CA377156123 | PSAP | c.99C>G (p.Cys33Trp)
| |
10 | g.71834447G>T | CA377156124 | PSAP | c.99C>A (p.Cys33Ter)
| |
10 | g.71834448C>A | CA377156125 | PSAP | c.98G>T (p.Cys33Phe)
| |
10 | g.71834448C>G | CA377156126 | PSAP | c.98G>C (p.Cys33Ser)
| |
10 | g.71834448C>T | CA377156128 | PSAP | c.98G>A (p.Cys33Tyr)
| |
10 | g.71834449A>C | CA377156140 | PSAP | c.97T>G (p.Cys33Gly)
| |
10 | g.71834449A>G | CA377156134 | PSAP | c.97T>C (p.Cys33Arg)
| |
10 | g.71834449A>T | CA377156132 | PSAP | c.97T>A (p.Cys33Ser)
| |
10 | g.71834450C>A | CA377156143 | PSAP | c.96G>T (p.Trp32Cys)
| |
10 | g.71834450C>G | CA377156146 | PSAP | c.96G>C (p.Trp32Cys)
| |
10 | g.71834450C>T | CA377156148 | PSAP | c.96G>A (p.Trp32Ter)
| |
10 | g.71834451C>A | CA377156151 | PSAP | c.95G>T (p.Trp32Leu)
| |
10 | g.71834451C>G | CA377156154 | PSAP | c.95G>C (p.Trp32Ser)
| |
10 | g.71834451C>T | CA377156157 | PSAP | c.95G>A (p.Trp32Ter)
| |
10 | g.71834451_71834454delinsCACA | CA1918891119 | PSAP | c.92_95delinsTGTG (p.Val31=)
| |
10 | g.71834452A= | CA1918891122 | PSAP | c.94T= (p.Trp32=)
| |
10 | g.71834452A>C | CA5547905 | PSAP | c.94T>G (p.Trp32Gly)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.71834452A>G | CA377156159 | PSAP | c.94T>C (p.Trp32Arg)
| |
10 | g.71834452A>T | CA377156158 | PSAP | c.94T>A (p.Trp32Arg)
| |
10 | g.71834452_71834454del | CA668091067 | PSAP | c.92_94del (p.Val31_Trp32delinsGly)
| dbSNP gnomAD v3 gnomAD v4 |
10 | g.71834453C>A | CA470061864 | PSAP | c.93G>T (p.Val31=)
| |
10 | g.71834453C>G | CA470061865 | PSAP | c.93G>C (p.Val31=)
| |
10 | g.71834453C>T | CA470061866 | PSAP | c.93G>A (p.Val31=)
| gnomAD v4 |
10 | g.71834454A>C | CA377156162 | PSAP | c.92T>G (p.Val31Gly)
| |
10 | g.71834454A>G | CA377156164 | PSAP | c.92T>C (p.Val31Ala)
| |
10 | g.71834454A>T | CA377156165 | PSAP | c.92T>A (p.Val31Glu)
| |
10 | g.71834455C>A | CA377156172 | PSAP | c.91G>T (p.Val31Leu)
| |
10 | g.71834455C>G | CA377156175 | PSAP | c.91G>C (p.Val31Leu)
| |
10 | g.71834455C>T | CA377156176 | PSAP | c.91G>A (p.Val31Met)
| |
10 | g.71834456T>A | CA470061870 | PSAP | c.90A>T (p.Ala30=)
| |
10 | g.71834456T>C | CA470061871 | PSAP | c.90A>G (p.Ala30=)
| |
10 | g.71834456T>G | CA470061873 | PSAP | c.90A>C (p.Ala30=)
| ClinVar dbSNP |
10 | g.71834457G>A | CA209472001 | PSAP | c.89C>T (p.Ala30Val)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
10 | g.71834457G>C | CA377156177 | PSAP | c.89C>G (p.Ala30Gly)
| |
10 | g.71834457G= | CA1918891124 | PSAP | c.89C= (p.Ala30=)
| |
10 | g.71834457G>T | CA377156178 | PSAP | c.89C>A (p.Ala30Glu)
| |
10 | g.71834458C>A | CA5547906 | PSAP | c.88G>T (p.Ala30Ser)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.71834458C= | CA1918891125 | PSAP | c.88G= (p.Ala30=)
| |
10 | g.71834458C>G | CA377156179 | PSAP | c.88G>C (p.Ala30Pro)
| |
10 | g.71834458C>T | CA377156180 | PSAP | c.88G>A (p.Ala30Thr)
| |
10 | g.71834459C>A | CA470061874 | PSAP | c.87G>T (p.Ser29=)
| |
10 | g.71834459C= | CA1918891128 | PSAP | c.87G= (p.Ser29=)
| |
10 | g.71834459C>G | CA5547908 | PSAP | c.87G>C (p.Ser29=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.71834459C>T | CA5547907 | PSAP | c.87G>A (p.Ser29=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.71834460G>A | CA5547909 | PSAP | c.86C>T (p.Ser29Leu)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.71834460G>C | CA377156187 | PSAP | c.86C>G (p.Ser29Trp)
| ClinVar gnomAD v4 |
10 | g.71834460G= | CA1918891131 | PSAP | c.86C= (p.Ser29=)
| |
10 | g.71834460G>T | CA377156189 | PSAP | c.86C>A (p.Ser29Ter)
| |
10 | g.71834461A>C | CA377156191 | PSAP | c.85T>G (p.Ser29Ala)
| |
10 | g.71834461A>G | CA377156193 | PSAP | c.85T>C (p.Ser29Pro)
| |
10 | g.71834461A>T | CA377156196 | PSAP | c.85T>A (p.Ser29Thr)
| |
10 | g.71834462G>A | CA470061880 | PSAP | c.84C>T (p.Gly28=)
| ClinVar dbSNP |
10 | g.71834462G>C | CA470061877 | PSAP | c.84C>G (p.Gly28=)
| |
10 | g.71834462G>T | CA470061879 | PSAP | c.84C>A (p.Gly28=)
| |
10 | g.71834463C>A | CA5547910 | PSAP | c.83G>T (p.Gly28Val)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.71834463C= | CA1918891133 | PSAP | c.83G= (p.Gly28=)
| |
10 | g.71834463C>G | CA377156205 | PSAP | c.83G>C (p.Gly28Ala)
| |
10 | g.71834463C>T | CA377156208 | PSAP | c.83G>A (p.Gly28Asp)
| |
10 | g.71834466del | CA2573145300 | PSAP | c.83del (p.Gly28AlafsTer9)
| ClinVar dbSNP |
10 | g.71834464C>A | CA377156215 | PSAP | c.82G>T (p.Gly28Cys)
| gnomAD v4 |
10 | g.71834464C>G | CA377156216 | PSAP | c.82G>C (p.Gly28Arg)
| |
10 | g.71834464C>T | CA377156221 | PSAP | c.82G>A (p.Gly28Ser)
| |
10 | g.71834465C>A | CA377156223 | PSAP | c.81G>T (p.Arg27Ser)
| |
10 | g.71834465C>G | CA377156230 | PSAP | c.81G>C (p.Arg27Ser)
| gnomAD v4 |
10 | g.71834465C>T | CA470061883 | PSAP | c.81G>A (p.Arg27=)
| gnomAD v4 |
10 | g.71834466C>A | CA377156243 | PSAP | c.80G>T (p.Arg27Met)
| |
10 | g.71834466C= | CA1918891134 | PSAP | c.80G= (p.Arg27=)
| |
10 | g.71834466C>G | CA377156240 | PSAP | c.80G>C (p.Arg27Thr)
| |
10 | g.71834466C>T | CA209472050 | PSAP | c.80G>A (p.Arg27Lys)
| dbSNP gnomAD v3 gnomAD v4 |
10 | g.71834467T>A | CA377156244 | PSAP | c.79A>T (p.Arg27Trp)
| |
10 | g.71834467T>C | CA209472056 | PSAP | c.79A>G (p.Arg27Gly)
| dbSNP |
10 | g.71834467T>G | CA470061884 | PSAP | c.79A>C (p.Arg27=)
| |
10 | g.71834467T= | CA1918891135 | PSAP | c.79A= (p.Arg27=)
| |
10 | g.71834468G>A | CA5547911 | PSAP | c.78C>T (p.Thr26=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.71834468G>C | CA470061888 | PSAP | c.78C>G (p.Thr26=)
| |
10 | g.71834468G= | CA1918891138 | PSAP | c.78C= (p.Thr26=)
| |
10 | g.71834468G>T | CA470061889 | PSAP | c.78C>A (p.Thr26=)
| |
10 | g.71834469G>A | CA377156251 | PSAP | c.77C>T (p.Thr26Ile)
| dbSNP |
10 | g.71834469G>C | CA5547912 | PSAP | c.77C>G (p.Thr26Ser)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.71834469G= | CA1918891141 | PSAP | c.77C= (p.Thr26=)
| |
10 | g.71834469G>T | CA377156255 | PSAP | c.77C>A (p.Thr26Asn)
| |
10 | g.71834470T>A | CA377156257 | PSAP | c.76A>T (p.Thr26Ser)
| |
10 | g.71834470T>C | CA377156259 | PSAP | c.76A>G (p.Thr26Ala)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
10 | g.71834470T>G | CA377156261 | PSAP | c.76A>C (p.Thr26Pro)
| |
10 | g.71834470T= | CA1918891143 | PSAP | c.76A= (p.Thr26=)
| |
10 | g.71834471G>A | CA209472081 | PSAP | c.75C>T (p.Cys25=)
| ClinVar dbSNP |
10 | g.71834471G>C | CA377156263 | PSAP | c.75C>G (p.Cys25Trp)
| |
10 | g.71834471G= | CA1918891145 | PSAP | c.75C= (p.Cys25=)
| |
10 | g.71834471G>T | CA377156267 | PSAP | c.75C>A (p.Cys25Ter)
| |
10 | g.71834472C>A | CA377156271 | PSAP | c.74G>T (p.Cys25Phe)
| |
10 | g.71834472C= | CA1918891148 | PSAP | c.74G= (p.Cys25=)
| |
10 | g.71834472C>G | CA377156273 | PSAP | c.74G>C (p.Cys25Ser)
| |
10 | g.71834472C>T | CA5547913 | PSAP | c.74G>A (p.Cys25Tyr)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.71834473A= | CA1918891151 | PSAP | c.73T= (p.Cys25=)
| |
10 | g.71834473A>C | CA377156286 | PSAP | c.73T>G (p.Cys25Gly)
| |
10 | g.71834473A>G | CA5547914 | PSAP | c.73T>C (p.Cys25Arg)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.71834473A>T | CA377156283 | PSAP | c.73T>A (p.Cys25Ser)
| |
10 | g.71834474T>A | CA377156289 | PSAP | c.72A>T (p.Glu24Asp)
| |
10 | g.71834474T>C | CA470061892 | PSAP | c.72A>G (p.Glu24=)
| |
10 | g.71834474T>G | CA377156292 | PSAP | c.72A>C (p.Glu24Asp)
| |
10 | g.71834475T>A | CA377156297 | PSAP | c.71A>T (p.Glu24Val)
| |
10 | g.71834475T>C | CA377156300 | PSAP | c.71A>G (p.Glu24Gly)
| |
10 | g.71834475T>G | CA377156302 | PSAP | c.71A>C (p.Glu24Ala)
| |
10 | g.71834476C>A | CA377156309 | PSAP | c.70G>T (p.Glu24Ter)
| |
10 | g.71834476C= | CA1918891153 | PSAP | c.70G= (p.Glu24=)
| |
10 | g.71834476C>G | CA377156308 | PSAP | c.70G>C (p.Glu24Gln)
| |
10 | g.71834476C>T | CA377156306 | PSAP | c.70G>A (p.Glu24Lys)
| |
10 | g.71834477T>A | CA377156314 | PSAP | c.69A>T (p.Lys23Asn)
| |
10 | g.71834477T>C | CA470061896 | PSAP | c.69A>G (p.Lys23=)
| ClinVar dbSNP gnomAD v4 |
10 | g.71834477T>G | CA377156317 | PSAP | c.69A>C (p.Lys23Asn)
| |
10 | g.71834477T= | CA1918891156 | PSAP | c.69A= (p.Lys23=)
| |
10 | g.71834479dup | CA209472089 | PSAP | c.69dup (p.Glu24ArgfsTer?)
| dbSNP |
10 | g.71834478T>A | CA377156321 | PSAP | c.68A>T (p.Lys23Ile)
| |
10 | g.71834478T>C | CA377156322 | PSAP | c.68A>G (p.Lys23Arg)
| |
10 | g.71834478T>G | CA377156326 | PSAP | c.68A>C (p.Lys23Thr)
| |
10 | g.71834479T>A | CA377156331 | PSAP | c.67A>T (p.Lys23Ter)
| |
10 | g.71834479T>C | CA5547915 | PSAP | c.67A>G (p.Lys23Glu)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.71834479T>G | CA377156330 | PSAP | c.67A>C (p.Lys23Gln)
| |
10 | g.71834479T= | CA1918891161 | PSAP | c.67A= (p.Lys23=)
| |
10 | g.71834480C>A | CA470061899 | PSAP | c.66G>T (p.Leu22=)
| |
10 | g.71834480C>G | CA470061900 | PSAP | c.66G>C (p.Leu22=)
| |
10 | g.71834480C>T | CA470061901 | PSAP | c.66G>A (p.Leu22=)
| |
10 | g.71834481A>C | CA377156332 | PSAP | c.65T>G (p.Leu22Arg)
| |
10 | g.71834481A>G | CA377156333 | PSAP | c.65T>C (p.Leu22Pro)
| |
10 | g.71834481A>T | CA377156334 | PSAP | c.65T>A (p.Leu22Gln)
| |
10 | g.71834482G>A | CA470061904 | PSAP | c.64C>T (p.Leu22=)
| |
10 | g.71834482G>C | CA377156335 | PSAP | c.64C>G (p.Leu22Val)
| |
10 | g.71834482G>T | CA377156336 | PSAP | c.64C>A (p.Leu22Met)
| |
10 | g.71834483T>A | CA470061908 | PSAP | c.63A>T (p.Gly21=)
| |
10 | g.71834483T>C | CA470061906 | PSAP | c.63A>G (p.Gly21=)
| |
10 | g.71834483T>G | CA470061907 | PSAP | c.63A>C (p.Gly21=)
| |
10 | g.71834484C>A | CA5547916 | PSAP | c.62G>T (p.Gly21Val)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.71834484C= | CA1918891163 | PSAP | c.62G= (p.Gly21=)
| |
10 | g.71834484C>G | CA377156338 | PSAP | c.62G>C (p.Gly21Ala)
| |
10 | g.71834484C>T | CA377156339 | PSAP | c.62G>A (p.Gly21Glu)
| |
10 | g.71834484_71834485dup | CA2741106174 | PSAP | c.61_62dup (p.Leu22AspfsTer2)
| |
10 | g.71834485C>A | CA377156342 | PSAP | c.61G>T (p.Gly21Ter)
| |
10 | g.71834485C>G | CA377156344 | PSAP | c.61G>C (p.Gly21Arg)
| |
10 | g.71834485C>T | CA377156345 | PSAP | c.61G>A (p.Gly21Arg)
| gnomAD v4 |
10 | g.71834486A= | CA1918891166 | PSAP | c.60T= (p.Leu20=)
| |
10 | g.71834486A>C | CA470061911 | PSAP | c.60T>G (p.Leu20=)
| |
10 | g.71834486A>G | CA5547917 | PSAP | c.60T>C (p.Leu20=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.71834486A>T | CA470061912 | PSAP | c.60T>A (p.Leu20=)
| |
10 | g.71834487A>C | CA377156346 | PSAP | c.59T>G (p.Leu20Arg)
| |
10 | g.71834487A>G | CA377156348 | PSAP | c.59T>C (p.Leu20Pro)
| |
10 | g.71834487A>T | CA377156347 | PSAP | c.59T>A (p.Leu20His)
| |
10 | g.71834488G>A | CA377156349 | PSAP | c.58C>T (p.Leu20Phe)
| |
10 | g.71834488G>C | CA377156351 | PSAP | c.58C>G (p.Leu20Val)
| gnomAD v4 |
10 | g.71834488G>T | CA377156350 | PSAP | c.58C>A (p.Leu20Ile)
| |
10 | g.71834489G>A | CA470061914 | PSAP | c.57C>T (p.Val19=)
| ClinVar |
10 | g.71834489G>C | CA470061915 | PSAP | c.57C>G (p.Val19=)
| |
10 | g.71834489G>T | CA470061916 | PSAP | c.57C>A (p.Val19=)
| ClinVar dbSNP gnomAD v4 |
10 | g.71834490A>C | CA377156353 | PSAP | c.56T>G (p.Val19Gly)
| |
10 | g.71834490A>G | CA377156354 | PSAP | c.56T>C (p.Val19Ala)
| |
10 | g.71834490A>T | CA377156356 | PSAP | c.56T>A (p.Val19Asp)
| |
10 | g.71834491C>A | CA377156358 | PSAP | c.55G>T (p.Val19Phe)
| |
10 | g.71834491C= | CA1918891168 | PSAP | c.55G= (p.Val19=)
| |
10 | g.71834491C>G | CA5547918 | PSAP | c.55G>C (p.Val19Leu)
| dbSNP ExAC gnomAD v2 |
10 | g.71834491C>T | CA377156362 | PSAP | c.55G>A (p.Val19Ile)
| |
10 | g.71834492C>A | CA470061920 | PSAP | c.54G>T (p.Pro18=)
| dbSNP gnomAD v3 gnomAD v4 |
10 | g.71834492C= | CA1918891171 | PSAP | c.54G= (p.Pro18=)
| |
10 | g.71834492C>G | CA470061921 | PSAP | c.54G>C (p.Pro18=)
| ClinVar dbSNP gnomAD v4 |
10 | g.71834492C>T | CA5547919 | PSAP | c.54G>A (p.Pro18=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
10 | g.71834493G>A | CA5547920 | PSAP | c.53C>T (p.Pro18Leu)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.71834493G>C | CA377156364 | PSAP | c.53C>G (p.Pro18Arg)
| gnomAD v4 |
10 | g.71834493G= | CA1918891174 | PSAP | c.53C= (p.Pro18=)
| |
10 | g.71834493G>T | CA377156365 | PSAP | c.53C>A (p.Pro18Gln)
| dbSNP gnomAD v4 |
10 | g.71834494G>A | CA377156367 | PSAP | c.52C>T (p.Pro18Ser)
| |
10 | g.71834494G>C | CA209472135 | PSAP | c.52C>G (p.Pro18Ala)
| ClinVar dbSNP gnomAD v4 |
10 | g.71834494G= | CA1918891178 | PSAP | c.52C= (p.Pro18=)
| |
10 | g.71834494G>T | CA377156370 | PSAP | c.52C>A (p.Pro18Thr)
| |
10 | g.71834495G>A | CA470061939 | PSAP | c.51C>T (p.Gly17=)
| |
10 | g.71834495G>C | CA470061940 | PSAP | c.51C>G (p.Gly17=)
| |
10 | g.71834495G>T | CA470061941 | PSAP | c.51C>A (p.Gly17=)
| |
10 | g.71834496C>A | CA377156372 | PSAP | c.50G>T (p.Gly17Val)
| |
10 | g.71834496C>G | CA377156379 | PSAP | c.50G>C (p.Gly17Ala)
| |
10 | g.71834496C>T | CA377156376 | PSAP | c.50G>A (p.Gly17Asp)
| |
10 | g.71834497C>A | CA377156381 | PSAP | c.49G>T (p.Gly17Cys)
| COSMIC |
10 | g.71834497C= | CA1918891181 | PSAP | c.49G= (p.Gly17=)
| |
10 | g.71834497C>G | CA377156387 | PSAP | c.49G>C (p.Gly17Arg)
| |
10 | g.71834497C>T | CA5547921 | PSAP | c.49G>A (p.Gly17Ser)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.71834498G>A | CA5547922 | PSAP | c.48C>T (p.Ala16=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
10 | g.71834498G>C | CA470061946 | PSAP | c.48C>G (p.Ala16=)
| |
10 | g.71834498G= | CA1918891184 | PSAP | c.48C= (p.Ala16=)
| |
10 | g.71834498G>T | CA470061948 | PSAP | c.48C>A (p.Ala16=)
| ClinVar |