Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.1401316_1401341delinsGCCAGCGCGTGCATATAGGGGGTCTCCA2317700385GAMTc.136_161delinsGAGACCCCCTATATGCACGCGCTGGC (p.Glu46=)
c.112+24_112+49delinsGAGACCCCCTATATGCACGCGCTGGC (n.112+24_112+49delinsGAGACCCCCTATATGCACGCGCTGGC)
19g.1401324_1401348delCA631301059GAMTc.136_160del (p.Glu46ProfsTer?)
c.112+24_112+48del (n.112+24_112+48del)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401329_1401333delCA2582641915GAMTc.144_148del (p.Tyr49AlafsTer?)
c.112+32_112+36del (n.112+32_112+36del)
gnomAD v4
19g.1401331T>ACA402998067GAMTc.146A>T (p.Tyr49Phe)
c.112+34A>T (n.112+34A>T)
gnomAD v4
19g.1401331T>CCA402998068GAMTc.146A>G (p.Tyr49Cys)
c.112+34A>G (n.112+34A>G)
gnomAD v4
19g.1401331T>GCA402998069GAMTc.146A>C (p.Tyr49Ser)
c.112+34A>C (n.112+34A>C)
19g.1401331_1401332delinsTACA2317700397GAMTc.145_146delinsTA (p.Tyr49=)
c.112+33_112+34delinsTA (n.112+33_112+34delinsTA)
19g.1401332delCA631301060GAMTc.145del (p.Tyr49IlefsTer?)
c.112+33del (n.112+33del)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.1401332A=CA2317700398GAMTc.145T= (p.Tyr49=)
c.112+33T= (n.112+33T=)
19g.1401332A>CCA402998072GAMTc.145T>G (p.Tyr49Asp)
c.112+33T>G (n.112+33T>G)
19g.1401332A>GCA402998071GAMTc.145T>C (p.Tyr49His)
c.112+33T>C (n.112+33T>C)
gnomAD v4
19g.1401332A>TCA402998070GAMTc.145T>A (p.Tyr49Asn)
c.112+33T>A (n.112+33T>A)
gnomAD v4
19g.1401333G>ACA504731621GAMTc.144C>T (p.Pro48=)
c.112+32C>T (n.112+32C>T)
ClinVar gnomAD v4
19g.1401333G>CCA504731619GAMTc.144C>G (p.Pro48=)
c.112+32C>G (n.112+32C>G)
19g.1401333G>TCA504731620GAMTc.144C>A (p.Pro48=)
c.112+32C>A (n.112+32C>A)
gnomAD v4
19g.1401337dupCA2317700399GAMTc.144dup (p.Tyr49LeufsTer?)
c.112+32dup (n.112+32dup)
ClinVar dbSNP gnomAD v4
19g.1401337delCA2582641916GAMTc.144del (p.Tyr49IlefsTer?)
c.112+32del (n.112+32del)
ClinVar gnomAD v4
19g.1401334G>ACA402998074GAMTc.143C>T (p.Pro48Leu)
c.112+31C>T (n.112+31C>T)
gnomAD v4
19g.1401334G>CCA402998073GAMTc.143C>G (p.Pro48Arg)
c.112+31C>G (n.112+31C>G)
19g.1401334G>TCA402998075GAMTc.143C>A (p.Pro48His)
c.112+31C>A (n.112+31C>A)
gnomAD v4
19g.1401335G>ACA402998076GAMTc.142C>T (p.Pro48Ser)
c.112+30C>T (n.112+30C>T)
ClinVar dbSNP gnomAD v4
19g.1401335G>CCA402998077GAMTc.142C>G (p.Pro48Ala)
c.112+30C>G (n.112+30C>G)
19g.1401335G>TCA402998078GAMTc.142C>A (p.Pro48Thr)
c.112+30C>A (n.112+30C>A)
gnomAD v4
19g.1401336G>ACA504731623GAMTc.141C>T (p.Thr47=)
c.112+29C>T (n.112+29C>T)
gnomAD v4
19g.1401336G>CCA504731624GAMTc.141C>G (p.Thr47=)
c.112+29C>G (n.112+29C>G)
ClinVar dbSNP gnomAD v4
19g.1401336G=CA2317700400GAMTc.141C= (p.Thr47=)
c.112+29C= (n.112+29C=)
19g.1401336G>TCA504731622GAMTc.141C>A (p.Thr47=)
c.112+29C>A (n.112+29C>A)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.1401337G>ACA10651551GAMTc.140C>T (p.Thr47Ile)
c.112+28C>T (n.112+28C>T)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.1401337G>CCA402998079GAMTc.140C>G (p.Thr47Ser)
c.112+28C>G (n.112+28C>G)
19g.1401337G=CA2317700401GAMTc.140C= (p.Thr47=)
c.112+28C= (n.112+28C=)
19g.1401337G>TCA402998080GAMTc.140C>A (p.Thr47Asn)
c.112+28C>A (n.112+28C>A)
gnomAD v4
19g.1401338T>ACA402998083GAMTc.139A>T (p.Thr47Ser)
c.112+27A>T (n.112+27A>T)
19g.1401338T>CCA402998081GAMTc.139A>G (p.Thr47Ala)
c.112+27A>G (n.112+27A>G)
gnomAD v4
19g.1401338T>GCA402998082GAMTc.139A>C (p.Thr47Pro)
c.112+27A>C (n.112+27A>C)
19g.1401339C>ACA402998084GAMTc.138G>T (p.Glu46Asp)
c.112+26G>T (n.112+26G>T)
gnomAD v4
19g.1401339C=CA2317700402GAMTc.138G= (p.Glu46=)
c.112+26G= (n.112+26G=)
19g.1401339C>GCA402998085GAMTc.138G>C (p.Glu46Asp)
c.112+26G>C (n.112+26G>C)
19g.1401339C>TCA504731625GAMTc.138G>A (p.Glu46=)
c.112+26G>A (n.112+26G>A)
ClinVar dbSNP gnomAD v4
19g.1401340T>ACA402998086GAMTc.137A>T (p.Glu46Val)
c.112+25A>T (n.112+25A>T)
19g.1401340T>CCA402998087GAMTc.137A>G (p.Glu46Gly)
c.112+25A>G (n.112+25A>G)
gnomAD v4
19g.1401340T>GCA402998088GAMTc.137A>C (p.Glu46Ala)
c.112+25A>C (n.112+25A>C)
19g.1401341C>ACA402998089GAMTc.136G>T (p.Glu46Ter)
c.112+24G>T (n.112+24G>T)
gnomAD v4
19g.1401341C>GCA402998091GAMTc.136G>C (p.Glu46Gln)
c.112+24G>C (n.112+24G>C)
19g.1401341C>TCA402998090GAMTc.136G>A (p.Glu46Lys)
c.112+24G>A (n.112+24G>A)
gnomAD v4
19g.1401342C>ACA402998092GAMTc.135G>T (p.Trp45Cys)
c.112+23G>T (n.112+23G>T)
gnomAD v4
19g.1401342C>GCA402998093GAMTc.135G>C (p.Trp45Cys)
c.112+23G>C (n.112+23G>C)
gnomAD v4
19g.1401342C>TCA402998094GAMTc.135G>A (p.Trp45Ter)
c.112+23G>A (n.112+23G>A)
gnomAD v4
19g.1401345_1401352dupCA2580096095GAMTc.128_135dup (p.Glu46SerfsTer?)
c.112+16_112+23dup (n.112+16_112+23dup)
ClinVar
19g.1401343C>ACA304067273GAMTc.134G>T (p.Trp45Leu)
c.112+22G>T (n.112+22G>T)
dbSNP gnomAD v2 gnomAD v4
19g.1401343C=CA2317700403GAMTc.134G= (p.Trp45=)
c.112+22G= (n.112+22G=)
19g.1401343C>GCA402998095GAMTc.134G>C (p.Trp45Ser)
c.112+22G>C (n.112+22G>C)
19g.1401343C>TCA402998096GAMTc.134G>A (p.Trp45Ter)
c.112+22G>A (n.112+22G>A)
ClinVar gnomAD v4
19g.1401344A=CA2317700404GAMTc.133T= (p.Trp45=)
c.112+21T= (n.112+21T=)
19g.1401344A>CCA402998097GAMTc.133T>G (p.Trp45Gly)
c.112+21T>G (n.112+21T>G)
19g.1401344A>GCA402998098GAMTc.133T>C (p.Trp45Arg)
c.112+21T>C (n.112+21T>C)
gnomAD v4
19g.1401344A>TCA10651554GAMTc.133T>A (p.Trp45Arg)
c.112+21T>A (n.112+21T>A)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401345G>ACA9043798GAMTc.132C>T (p.Arg44=)
c.112+20C>T (n.112+20C>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.1401345G>CCA504731626GAMTc.132C>G (p.Arg44=)
c.112+20C>G (n.112+20C>G)
gnomAD v4
19g.1401345G=CA2317700405GAMTc.132C= (p.Arg44=)
c.112+20C= (n.112+20C=)
19g.1401345G>TCA504731627GAMTc.132C>A (p.Arg44=)
c.112+20C>A (n.112+20C>A)
gnomAD v4
19g.1401346C>ACA9043799GAMTc.131G>T (p.Arg44Leu)
c.112+19G>T (n.112+19G>T)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.1401346C=CA2317700406GAMTc.131G= (p.Arg44=)
c.112+19G= (n.112+19G=)
19g.1401346C>GCA402998099GAMTc.131G>C (p.Arg44Pro)
c.112+19G>C (n.112+19G>C)
ClinVar dbSNP gnomAD v4
19g.1401346C>TCA9043800GAMTc.131G>A (p.Arg44His)
c.112+19G>A (n.112+19G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.1401347G>ACA402998100GAMTc.130C>T (p.Arg44Cys)
c.112+18C>T (n.112+18C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401347G>CCA402998101GAMTc.130C>G (p.Arg44Gly)
c.112+18C>G (n.112+18C>G)
ClinVar
19g.1401347G=CA2317700407GAMTc.130C= (p.Arg44=)
c.112+18C= (n.112+18C=)
19g.1401347G>TCA402998102GAMTc.130C>A (p.Arg44Ser)
c.112+18C>A (n.112+18C>A)
dbSNP gnomAD v2 gnomAD v4
19g.1401348C>ACA402998103GAMTc.129G>T (p.Glu43Asp)
c.112+17G>T (n.112+17G>T)
gnomAD v4
19g.1401348C>GCA402998104GAMTc.129G>C (p.Glu43Asp)
c.112+17G>C (n.112+17G>C)
19g.1401348C>TCA504731628GAMTc.129G>A (p.Glu43=)
c.112+17G>A (n.112+17G>A)
gnomAD v4
19g.1401349T>ACA402998106GAMTc.128A>T (p.Glu43Val)
c.112+16A>T (n.112+16A>T)
gnomAD v4
19g.1401349T>CCA314848GAMTc.128A>G (p.Glu43Gly)
c.112+16A>G (n.112+16A>G)
ClinVar dbSNP gnomAD v4
19g.1401349T>GCA402998105GAMTc.128A>C (p.Glu43Ala)
c.112+16A>C (n.112+16A>C)
gnomAD v4
19g.1401349T=CA2317700408GAMTc.128A= (p.Glu43=)
c.112+16A= (n.112+16A=)
19g.1401350C>ACA402998107GAMTc.127G>T (p.Glu43Ter)
c.112+15G>T (n.112+15G>T)
gnomAD v4
19g.1401350C=CA2317700409GAMTc.127G= (p.Glu43=)
c.112+15G= (n.112+15G=)
19g.1401350C>GCA9043801GAMTc.127G>C (p.Glu43Gln)
c.112+15G>C (n.112+15G>C)
ClinVar dbSNP ExAC gnomAD v2
19g.1401350C>TCA402998108GAMTc.127G>A (p.Glu43Lys)
c.112+15G>A (n.112+15G>A)
gnomAD v4
19g.1401351C>ACA402998109GAMTc.126G>T (p.Met42Ile)
c.112+14G>T (n.112+14G>T)
gnomAD v4
19g.1401351C>GCA402998110GAMTc.126G>C (p.Met42Ile)
c.112+14G>C (n.112+14G>C)
19g.1401351C>TCA402998111GAMTc.126G>A (p.Met42Ile)
c.112+14G>A (n.112+14G>A)
gnomAD v4
19g.1401352A=CA2317700410GAMTc.125T= (p.Met42=)
c.112+13T= (n.112+13T=)
19g.1401352A>CCA402998112GAMTc.125T>G (p.Met42Arg)
c.112+13T>G (n.112+13T>G)
19g.1401352A>GCA402998114GAMTc.125T>C (p.Met42Thr)
c.112+13T>C (n.112+13T>C)
dbSNP gnomAD v2 gnomAD v4
19g.1401352A>TCA402998113GAMTc.125T>A (p.Met42Lys)
c.112+13T>A (n.112+13T>A)
gnomAD v4
19g.1401353T>ACA402998115GAMTc.124A>T (p.Met42Leu)
c.112+12A>T (n.112+12A>T)
19g.1401353T>CCA314846GAMTc.124A>G (p.Met42Val)
c.112+12A>G (n.112+12A>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.1401353T>GCA402998116GAMTc.124A>C (p.Met42Leu)
c.112+12A>C (n.112+12A>C)
dbSNP
19g.1401353T=CA2317700411GAMTc.124A= (p.Met42=)
c.112+12A= (n.112+12A=)
19g.1401354C>ACA504731629GAMTc.123G>T (p.Val41=)
c.112+11G>T (n.112+11G>T)
gnomAD v4
19g.1401354C>GCA504731630GAMTc.123G>C (p.Val41=)
c.112+11G>C (n.112+11G>C)
19g.1401354C>TCA504731631GAMTc.123G>A (p.Val41=)
c.112+11G>A (n.112+11G>A)
gnomAD v4
19g.1401355A=CA2317700412GAMTc.122T= (p.Val41=)
c.112+10T= (n.112+10T=)
19g.1401355A>CCA402998117GAMTc.122T>G (p.Val41Gly)
c.112+10T>G (n.112+10T>G)
19g.1401355A>GCA402998118GAMTc.122T>C (p.Val41Ala)
c.112+10T>C (n.112+10T>C)
ClinVar dbSNP gnomAD v4
19g.1401355A>TCA402998119GAMTc.122T>A (p.Val41Glu)
c.112+10T>A (n.112+10T>A)
gnomAD v4
19g.1401356C>ACA402998120GAMTc.121G>T (p.Val41Leu)
c.112+9G>T (n.112+9G>T)
gnomAD v4
19g.1401356C>GCA402998121GAMTc.121G>C (p.Val41Leu)
c.112+9G>C (n.112+9G>C)
gnomAD v4
19g.1401356C>TCA402998122GAMTc.121G>A (p.Val41Met)
c.112+9G>A (n.112+9G>A)
gnomAD v4
19g.1401357C>ACA504731633GAMTc.120G>T (p.Pro40=)
c.112+8G>T (n.112+8G>T)
gnomAD v4
19g.1401357C>GCA504731634GAMTc.120G>C (p.Pro40=)
c.112+8G>C (n.112+8G>C)
19g.1401357C>TCA504731632GAMTc.120G>A (p.Pro40=)
c.112+8G>A (n.112+8G>A)
ClinVar dbSNP gnomAD v4
19g.1401358G>ACA402998123GAMTc.119C>T (p.Pro40Leu)
c.112+7C>T (n.112+7C>T)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.1401358G>CCA402998124GAMTc.119C>G (p.Pro40Arg)
c.112+7C>G (n.112+7C>G)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.1401358G=CA2317700413GAMTc.119C= (p.Pro40=)
c.112+7C= (n.112+7C=)
19g.1401358G>TCA402998125GAMTc.119C>A (p.Pro40Gln)
c.112+7C>A (n.112+7C>A)
dbSNP gnomAD v3 gnomAD v4
19g.1401359G>ACA304067305GAMTc.118C>T (p.Pro40Ser)
c.112+6C>T (n.112+6C>T)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401359G>CCA402998127GAMTc.118C>G (p.Pro40Ala)
c.112+6C>G (n.112+6C>G)
gnomAD v4
19g.1401359G=CA2317700414GAMTc.118C= (p.Pro40=)
c.112+6C= (n.112+6C=)
19g.1401359G>TCA402998126GAMTc.118C>A (p.Pro40Thr)
c.112+6C>A (n.112+6C>A)
gnomAD v4
19g.1401360C>ACA402998128GAMTc.117G>T (p.Lys39Asn)
c.112+5G>T (n.112+5G>T)
gnomAD v4
19g.1401360C>GCA402998129GAMTc.117G>C (p.Lys39Asn)
c.112+5G>C (n.112+5G>C)
19g.1401360C>TCA504731635GAMTc.117G>A (p.Lys39=)
c.112+5G>A (n.112+5G>A)
19g.1401361T>ACA402998130GAMTc.116A>T (p.Lys39Met)
c.112+4A>T (n.112+4A>T)
19g.1401361T>CCA402998132GAMTc.116A>G (p.Lys39Arg)
c.112+4A>G (n.112+4A>G)
19g.1401361T>GCA402998131GAMTc.116A>C (p.Lys39Thr)
c.112+4A>C (n.112+4A>C)
19g.1401362T>ACA402998133GAMTc.115A>T (p.Lys39Ter)
c.112+3A>T (n.112+3A>T)
19g.1401362T>CCA402998134GAMTc.115A>G (p.Lys39Glu)
c.112+3A>G (n.112+3A>G)
ClinVar gnomAD v4
19g.1401362T>GCA402998135GAMTc.115A>C (p.Lys39Gln)
c.112+3A>C (n.112+3A>C)
ClinVar dbSNP gnomAD v4
19g.1401365_1401373delCA2582641917GAMTc.107_115del (p.Ile36_Gly38del)
c.107_112+3del
gnomAD v4
19g.1401363G>ACA504731636GAMTc.114C>T (p.Gly38=)
c.112+2C>T (n.112+2C>T)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.1401363G>CCA504731638GAMTc.114C>G (p.Gly38=)
c.112+2C>G (n.112+2C>G)
19g.1401363G=CA2317700415GAMTc.114C= (p.Gly38=)
c.112+2C= (n.112+2C=)
19g.1401363G>TCA504731637GAMTc.114C>A (p.Gly38=)
c.112+2C>A (n.112+2C>A)
gnomAD v4
19g.1401364C>ACA402998136GAMTc.113G>T (p.Gly38Val)
c.112+1G>T (n.112+1G>T)
gnomAD v4
19g.1401364C>GCA402998137GAMTc.113G>C (p.Gly38Ala)
c.112+1G>C (n.112+1G>C)
gnomAD v4
19g.1401364C>TCA402998139GAMTc.113G>A (p.Gly38Asp)
c.112+1G>A (n.112+1G>A)
gnomAD v4
19g.1401366dupCA2695198106GAMTc.113dup (p.Lys39GlnfsTer?)
c.112+1dup
ClinVar
19g.1401366delCA2582641918GAMTc.113del (p.Gly38AlafsTer4)
c.112+1del
gnomAD v4
19g.1401365C>ACA402998140GAMTc.112G>T (p.Gly38Cys)
c.112G>T (p.Gly38Trp)
gnomAD v4
19g.1401365C=CA2317700416GAMTc.112G= (p.Gly38=)
19g.1401365C>GCA402998141GAMTc.112G>C (p.Gly38Arg)
dbSNP
19g.1401365C>TCA304067308GAMTc.112G>A (p.Gly38Ser)
c.112G>A (p.Gly38Arg)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401366C>ACA504731639GAMTc.111G>T (p.Leu37=)
gnomAD v4
19g.1401366C>GCA504731640GAMTc.111G>C (p.Leu37=)
19g.1401366C>TCA504731641GAMTc.111G>A (p.Leu37=)
gnomAD v4
19g.1401367A>CCA402998142GAMTc.110T>G (p.Leu37Arg)
gnomAD v4
19g.1401367A>GCA402998143GAMTc.110T>C (p.Leu37Pro)
gnomAD v4
19g.1401367A>TCA402998144GAMTc.110T>A (p.Leu37Gln)
gnomAD v4
19g.1401368G>ACA504731642GAMTc.109C>T (p.Leu37=)
gnomAD v4
19g.1401368G>CCA402998146GAMTc.109C>G (p.Leu37Val)
gnomAD v4
19g.1401368G=CA2317700417GAMTc.109C= (p.Leu37=)
19g.1401368G>TCA402998145GAMTc.109C>A (p.Leu37Met)
dbSNP gnomAD v4
19g.1401369G>ACA504731643GAMTc.108C>T (p.Ile36=)
ClinVar dbSNP gnomAD v4
19g.1401369G>CCA402998147GAMTc.108C>G (p.Ile36Met)
gnomAD v4
19g.1401369G>TCA504731644GAMTc.108C>A (p.Ile36=)
gnomAD v4
19g.1401370A>CCA402998148GAMTc.107T>G (p.Ile36Ser)
19g.1401370A>GCA402998149GAMTc.107T>C (p.Ile36Thr)
gnomAD v4
19g.1401370A>TCA402998150GAMTc.107T>A (p.Ile36Asn)
gnomAD v4
19g.1401371T>ACA402998152GAMTc.106A>T (p.Ile36Phe)
19g.1401371T>CCA402998154GAMTc.106A>G (p.Ile36Val)
ClinVar dbSNP gnomAD v4
19g.1401371T>GCA402998156GAMTc.106A>C (p.Ile36Leu)
19g.1401371T=CA2317700418GAMTc.106A= (p.Ile36=)
19g.1401372G>ACA9043802GAMTc.105C>T (p.Arg35=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.1401372G>CCA504731645GAMTc.105C>G (p.Arg35=)
gnomAD v4
19g.1401372G=CA2317700419GAMTc.105C= (p.Arg35=)
19g.1401372G>TCA504731646GAMTc.105C>A (p.Arg35=)
gnomAD v4
19g.1401373C>ACA402998160GAMTc.104G>T (p.Arg35Leu)
gnomAD v4
19g.1401373C>GCA402998161GAMTc.104G>C (p.Arg35Pro)
19g.1401373C>TCA402998163GAMTc.104G>A (p.Arg35His)
gnomAD v4
19g.1401374G>ACA402998168GAMTc.103C>T (p.Arg35Cys)
gnomAD v4
19g.1401374G>CCA402998167GAMTc.103C>G (p.Arg35Gly)
19g.1401374G>TCA402998165GAMTc.103C>A (p.Arg35Ser)
gnomAD v4
19g.1401375C>ACA9043803GAMTc.102G>T (p.Leu34=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.1401375C=CA2317700420GAMTc.102G= (p.Leu34=)
19g.1401375C>GCA504731647GAMTc.102G>C (p.Leu34=)
19g.1401375C>TCA504731648GAMTc.102G>A (p.Leu34=)
gnomAD v4
19g.1401376A=CA2317700421GAMTc.101T= (p.Leu34=)
19g.1401376A>CCA402998169GAMTc.101T>G (p.Leu34Arg)
19g.1401376A>GCA402998170GAMTc.101T>C (p.Leu34Pro)
dbSNP gnomAD v3 gnomAD v4
19g.1401376A>TCA402998172GAMTc.101T>A (p.Leu34Gln)
gnomAD v4
19g.1401377G>ACA504731649GAMTc.100C>T (p.Leu34=)
ClinVar dbSNP gnomAD v4
19g.1401377G>CCA402998174GAMTc.100C>G (p.Leu34Val)
gnomAD v4
19g.1401377G>TCA402998176GAMTc.100C>A (p.Leu34Met)
gnomAD v4
19g.1401378G>ACA504731650GAMTc.99C>T (p.His33=)
gnomAD v4
19g.1401378G>CCA402998178GAMTc.99C>G (p.His33Gln)
19g.1401378G>TCA402998177GAMTc.99C>A (p.His33Gln)
gnomAD v4
19g.1401379T>ACA402998181GAMTc.98A>T (p.His33Leu)
19g.1401379T>CCA402998182GAMTc.98A>G (p.His33Arg)
gnomAD v4
19g.1401379T>GCA402998183GAMTc.98A>C (p.His33Pro)
gnomAD v4
19g.1401380G>ACA402998185GAMTc.97C>T (p.His33Tyr)
dbSNP gnomAD v4
19g.1401380G>CCA402998187GAMTc.97C>G (p.His33Asp)
19g.1401380G=CA2317700422GAMTc.97C= (p.His33=)
19g.1401380G>TCA402998188GAMTc.97C>A (p.His33Asn)
gnomAD v4
19g.1401381C>ACA504731651GAMTc.96G>T (p.Thr32=)
gnomAD v4
19g.1401381C=CA2317700423GAMTc.96G= (p.Thr32=)
19g.1401381C>GCA504731653GAMTc.96G>C (p.Thr32=)
19g.1401381C>TCA504731652GAMTc.96G>A (p.Thr32=)
ClinVar dbSNP gnomAD v4
19g.1401382G>ACA402998190GAMTc.95C>T (p.Thr32Met)
gnomAD v4
19g.1401382G>CCA402998192GAMTc.95C>G (p.Thr32Arg)
gnomAD v4
19g.1401382G>TCA402998191GAMTc.95C>A (p.Thr32Lys)
gnomAD v4
19g.1401384_1401385delCA2582641919GAMTc.94_95del (p.Thr32AlafsTer?)
c.94_95del (p.Thr32AlafsTer29)
gnomAD v4
19g.1401383T>ACA402998193GAMTc.94A>T (p.Thr32Ser)
gnomAD v4
19g.1401383T>CCA402998195GAMTc.94A>G (p.Thr32Ala)
gnomAD v4
19g.1401383T>GCA402998196GAMTc.94A>C (p.Thr32Pro)
19g.1401384G>ACA504731654GAMTc.93C>T (p.Asp31=)
dbSNP gnomAD v3 gnomAD v4
19g.1401384G>CCA402998198GAMTc.93C>G (p.Asp31Glu)
19g.1401384G=CA2317700424GAMTc.93C= (p.Asp31=)
19g.1401384G>TCA402998200GAMTc.93C>A (p.Asp31Glu)
gnomAD v4
19g.1401385T>ACA314844GAMTc.92A>T (p.Asp31Val)
ClinVar dbSNP gnomAD v4
19g.1401385T>CCA402998201GAMTc.92A>G (p.Asp31Gly)
gnomAD v4
19g.1401385T>GCA402998202GAMTc.92A>C (p.Asp31Ala)
19g.1401385T=CA2317700425GAMTc.92A= (p.Asp31=)
19g.1401386C>ACA402998204GAMTc.91G>T (p.Asp31Tyr)
gnomAD v4
19g.1401386C>GCA402998206GAMTc.91G>C (p.Asp31His)
19g.1401386C>TCA402998210GAMTc.91G>A (p.Asp31Asn)
gnomAD v4
19g.1401388_1401389insTGCCGCA631301069GAMTc.91_92insCACGG (p.Asp31AlafsTer13)
c.91_92insCACGG (p.Asp31AlafsTer?)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.1401387C>ACA504731655GAMTc.90G>T (p.Ala30=)
gnomAD v4
19g.1401387C>GCA504731656GAMTc.90G>C (p.Ala30=)
gnomAD v4
19g.1401387C>TCA504731657GAMTc.90G>A (p.Ala30=)
ClinVar dbSNP gnomAD v4
19g.1401388_1401389delCA2582641920GAMTc.89_90del (p.Ala30GlyfsTer?)
gnomAD v4
19g.1401388G>ACA402998216GAMTc.89C>T (p.Ala30Val)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401388G>CCA402998215GAMTc.89C>G (p.Ala30Gly)
dbSNP gnomAD v3 gnomAD v4
19g.1401388G=CA2317700426GAMTc.89C= (p.Ala30=)
19g.1401388G>TCA402998213GAMTc.89C>A (p.Ala30Glu)
gnomAD v4
19g.1401389C>ACA402998220GAMTc.88G>T (p.Ala30Ser)
gnomAD v4
19g.1401389C=CA2317700427GAMTc.88G= (p.Ala30=)
19g.1401389C>GCA402998218GAMTc.88G>C (p.Ala30Pro)
dbSNP gnomAD v2 gnomAD v4
19g.1401389C>TCA402998221GAMTc.88G>A (p.Ala30Thr)
gnomAD v4
19g.1401390T>ACA504731660GAMTc.87A>T (p.Ala29=)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.1401390T>CCA504731661GAMTc.87A>G (p.Ala29=)
gnomAD v4
19g.1401390T>GCA504731659GAMTc.87A>C (p.Ala29=)
dbSNP gnomAD v2 gnomAD v4
19g.1401390T=CA2317700428GAMTc.87A= (p.Ala29=)
19g.1401391G>ACA402998223GAMTc.86C>T (p.Ala29Val)
gnomAD v4
19g.1401391G>CCA402998224GAMTc.86C>G (p.Ala29Gly)
19g.1401391G>TCA402998226GAMTc.86C>A (p.Ala29Glu)
gnomAD v4
19g.1401392C>ACA402998228GAMTc.85G>T (p.Ala29Ser)
gnomAD v4
19g.1401392C=CA2317700429GAMTc.85G= (p.Ala29=)
19g.1401392C>GCA402998230GAMTc.85G>C (p.Ala29Pro)
19g.1401392C>TCA402998231GAMTc.85G>A (p.Ala29Thr)
ClinVar dbSNP gnomAD v4
19g.1401393G>ACA9043804GAMTc.84C>T (p.Asp28=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.1401393G>CCA402998234GAMTc.84C>G (p.Asp28Glu)
19g.1401393G=CA2317700430GAMTc.84C= (p.Asp28=)
19g.1401393G>TCA402998236GAMTc.84C>A (p.Asp28Glu)
gnomAD v4
19g.1401394T>ACA402998237GAMTc.83A>T (p.Asp28Val)
19g.1401394T>CCA402998239GAMTc.83A>G (p.Asp28Gly)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401394T>GCA402998240GAMTc.83A>C (p.Asp28Ala)
dbSNP gnomAD v3 gnomAD v4
19g.1401394T=CA2317700431GAMTc.83A= (p.Asp28=)
19g.1401395C>ACA402998246GAMTc.82G>T (p.Asp28Tyr)
gnomAD v4
19g.1401395C=CA2317700432GAMTc.82G= (p.Asp28=)
19g.1401395C>GCA402998242GAMTc.82G>C (p.Asp28His)
dbSNP gnomAD v2 gnomAD v4
19g.1401395C>TCA402998244GAMTc.82G>A (p.Asp28Asn)
gnomAD v4
19g.1401395dupCA2580096099GAMTc.82dup (p.Asp28GlyfsTer?)
ClinVar
19g.1401396G>ACA504731663GAMTc.81C>T (p.Tyr27=)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC
19g.1401396G>CCA304067316GAMTc.81C>G (p.Tyr27Ter)
dbSNP gnomAD v3 gnomAD v4
19g.1401396G=CA2317700433GAMTc.81C= (p.Tyr27=)
19g.1401396G>TCA402998248GAMTc.81C>A (p.Tyr27Ter)
gnomAD v4
19g.1401396dupCA2582641921GAMTc.81dup (p.Asp28ArgfsTer?)
gnomAD v4
19g.1401397T>ACA9043805GAMTc.80A>T (p.Tyr27Phe)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.1401397T>CCA402998251GAMTc.80A>G (p.Tyr27Cys)
gnomAD v4
19g.1401397T>GCA402998253GAMTc.80A>C (p.Tyr27Ser)
19g.1401397T=CA2317700434GAMTc.80A= (p.Tyr27=)
19g.1401398A=CA2317700435GAMTc.79T= (p.Tyr27=)
19g.1401398A>CCA402998254GAMTc.79T>G (p.Tyr27Asp)
19g.1401398A>GCA295620GAMTc.79T>C (p.Tyr27His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.1401398A>TCA402998256GAMTc.79T>A (p.Tyr27Asn)
19g.1401399G>ACA504731665GAMTc.78C>T (p.Ala26=)
gnomAD v4
19g.1401399G>CCA504731666GAMTc.78C>G (p.Ala26=)
19g.1401399G>TCA504731667GAMTc.78C>A (p.Ala26=)
gnomAD v4
19g.1401400G>ACA402998258GAMTc.77C>T (p.Ala26Val)
gnomAD v4
19g.1401400G>CCA402998260GAMTc.77C>G (p.Ala26Gly)
gnomAD v4
19g.1401400G>TCA402998262GAMTc.77C>A (p.Ala26Asp)
gnomAD v4
19g.1401401C>ACA402998265GAMTc.76G>T (p.Ala26Ser)
dbSNP gnomAD v4
19g.1401401C=CA2317700436GAMTc.76G= (p.Ala26=)
19g.1401401C>GCA402998266GAMTc.76G>C (p.Ala26Pro)
19g.1401401C>TCA402998263GAMTc.76G>A (p.Ala26Thr)
gnomAD v4
19g.1401402C>ACA504731672GAMTc.75G>T (p.Ala25=)
gnomAD v4
19g.1401402C=CA2317700437GAMTc.75G= (p.Ala25=)
19g.1401402C>GCA504731673GAMTc.75G>C (p.Ala25=)
19g.1401402C>TCA9043806GAMTc.75G>A (p.Ala25=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.1401403G>ACA402998268GAMTc.74C>T (p.Ala25Val)
gnomAD v4
19g.1401403G>CCA402998270GAMTc.74C>G (p.Ala25Gly)
19g.1401403G=CA2317700438GAMTc.74C= (p.Ala25=)
19g.1401403G>TCA402998271GAMTc.74C>A (p.Ala25Glu)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401404delCA2582641922GAMTc.73del (p.Ala25ArgfsTer17)
c.73del (p.Ala25ArgfsTer?)
gnomAD v4
19g.1401404C>ACA9043807GAMTc.73G>T (p.Ala25Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.1401404C=CA2317700439GAMTc.73G= (p.Ala25=)
19g.1401404C>GCA402998274GAMTc.73G>C (p.Ala25Pro)
19g.1401404C>TCA402998276GAMTc.73G>A (p.Ala25Thr)
gnomAD v4
19g.1401406_1401509delCA2582641923GAMTc.-31_73del
gnomAD v4
19g.1401405G>ACA504731674GAMTc.72C>T (p.Pro24=)
gnomAD v4
19g.1401405G>CCA504731678GAMTc.72C>G (p.Pro24=)
19g.1401405G>TCA504731679GAMTc.72C>A (p.Pro24=)
ClinVar gnomAD v4
19g.1401407dupCA2813256122GAMTc.72dup (p.Ala25ArgfsTer?)
19g.1401407delCA2582641924GAMTc.72del (p.Ala25ArgfsTer17)
c.72del (p.Ala25ArgfsTer?)
gnomAD v4
19g.1401406G>ACA402998278GAMTc.71C>T (p.Pro24Leu)
gnomAD v4
19g.1401406G>CCA402998280GAMTc.71C>G (p.Pro24Arg)
gnomAD v4
19g.1401406G>TCA402998282GAMTc.71C>A (p.Pro24His)
gnomAD v4
19g.1401407G>ACA402998284GAMTc.70C>T (p.Pro24Ser)
gnomAD v4
19g.1401407G>CCA402998285GAMTc.70C>G (p.Pro24Ala)
19g.1401407G>TCA402998287GAMTc.70C>A (p.Pro24Thr)
gnomAD v4
19g.1401408C>ACA504731680GAMTc.69G>T (p.Ala23=)
gnomAD v4
19g.1401408C>GCA504731681GAMTc.69G>C (p.Ala23=)
ClinVar
19g.1401408C>TCA504731682GAMTc.69G>A (p.Ala23=)
gnomAD v4
19g.1401409G>ACA314842GAMTc.68C>T (p.Ala23Val)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401409G>CCA402998290GAMTc.68C>G (p.Ala23Gly)
dbSNP gnomAD v4
19g.1401409G=CA2317700440GAMTc.68C= (p.Ala23=)
19g.1401409G>TCA402998289GAMTc.68C>A (p.Ala23Glu)
gnomAD v4
19g.1401410C>ACA402998293GAMTc.67G>T (p.Ala23Ser)
gnomAD v4
19g.1401410C=CA2317700441GAMTc.67G= (p.Ala23=)
19g.1401410C>GCA402998295GAMTc.67G>C (p.Ala23Pro)
19g.1401410C>TCA9043808GAMTc.67G>A (p.Ala23Thr)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.1401411C>ACA504731684GAMTc.66G>T (p.Ala22=)
ClinVar gnomAD v4
19g.1401411C=CA2317700442GAMTc.66G= (p.Ala22=)
19g.1401411C>GCA504731685GAMTc.66G>C (p.Ala22=)
19g.1401411C>TCA9043809GAMTc.66G>A (p.Ala22=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.1401412_1401413delCA2582641925GAMTc.65_66del (p.Ala22GlyfsTer?)
gnomAD v4
19g.1401412delCA2580096101GAMTc.65del (p.Ala22GlyfsTer20)
c.65del (p.Ala22GlyfsTer?)
ClinVar gnomAD v4
19g.1401412G>ACA402998296GAMTc.65C>T (p.Ala22Val)
gnomAD v4
19g.1401412G>CCA402998298GAMTc.65C>G (p.Ala22Gly)
gnomAD v4
19g.1401412G>TCA402998300GAMTc.65C>A (p.Ala22Glu)
gnomAD v4
19g.1401412_1401413delinsGCCA2317700443GAMTc.64_65delinsGC (p.Ala22=)
19g.1401413C>ACA402998301GAMTc.64G>T (p.Ala22Ser)
gnomAD v4
19g.1401413C=CA2317700444GAMTc.64G= (p.Ala22=)
19g.1401413C>GCA402998303GAMTc.64G>C (p.Ala22Pro)
19g.1401413C>TCA10651555GAMTc.64G>A (p.Ala22Thr)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401418dupCA631301051GAMTc.64dup (p.Ala22GlyfsTer?)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
19g.1401417_1401418dupCA2582641926GAMTc.63_64dup (p.Ala22GlyfsTer21)
c.63_64dup (p.Ala22GlyfsTer?)
gnomAD v4
19g.1401418delCA631301050GAMTc.64del (p.Ala22ArgfsTer20)
c.64del (p.Ala22ArgfsTer?)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC
19g.1401414C>ACA504731691GAMTc.63G>T (p.Gly21=)
gnomAD v4
19g.1401414C>GCA504731692GAMTc.63G>C (p.Gly21=)
gnomAD v4
19g.1401414C>TCA504731693GAMTc.63G>A (p.Gly21=)
gnomAD v4
19g.1401415C>ACA402998306GAMTc.62G>T (p.Gly21Val)
gnomAD v4
19g.1401415C>GCA402998308GAMTc.62G>C (p.Gly21Ala)
19g.1401415C>TCA402998310GAMTc.62G>A (p.Gly21Glu)
ClinVar gnomAD v4
19g.1401416C>ACA402998314GAMTc.61G>T (p.Gly21Trp)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401416C=CA2317700445GAMTc.61G= (p.Gly21=)
19g.1401416C>GCA402998316GAMTc.61G>C (p.Gly21Arg)
gnomAD v4
19g.1401416C>TCA402998313GAMTc.61G>A (p.Gly21Arg)
gnomAD v4
19g.1401417C>ACA402998320GAMTc.60G>T (p.Trp20Cys)
gnomAD v4
19g.1401417C=CA2317700446GAMTc.60G= (p.Trp20=)
19g.1401417C>GCA402998323GAMTc.60G>C (p.Trp20Cys)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401417C>TCA402998322GAMTc.60G>A (p.Trp20Ter)
ClinVar gnomAD v4
19g.1401418C>ACA402998326GAMTc.59G>T (p.Trp20Leu)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.1401418C=CA2317700447GAMTc.59G= (p.Trp20=)
19g.1401418C>GCA340769GAMTc.59G>C (p.Trp20Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.1401418C>TCA402998328GAMTc.59G>A (p.Trp20Ter)
ClinVar dbSNP gnomAD v4
19g.1401419A>CCA402998332GAMTc.58T>G (p.Trp20Gly)
19g.1401419A>GCA402998334GAMTc.58T>C (p.Trp20Arg)
gnomAD v4
19g.1401419A>TCA402998333GAMTc.58T>A (p.Trp20Arg)
19g.1401419dupCA504731701GAMTc.58dup (p.Trp20LeufsTer?)
ClinVar gnomAD v4
19g.1401420C>ACA504731707GAMTc.57G>T (p.Ala19=)
gnomAD v4
19g.1401420C=CA2317700448GAMTc.57G= (p.Ala19=)
19g.1401420C>GCA504731706GAMTc.57G>C (p.Ala19=)
dbSNP gnomAD v3 gnomAD v4
19g.1401420C>TCA504731704GAMTc.57G>A (p.Ala19=)
gnomAD v4
19g.1401421G>ACA402998335GAMTc.56C>T (p.Ala19Val)
gnomAD v4
19g.1401421G>CCA402998336GAMTc.56C>G (p.Ala19Gly)
19g.1401421G>TCA402998337GAMTc.56C>A (p.Ala19Glu)
gnomAD v4
19g.1401422C>ACA402998341GAMTc.55G>T (p.Ala19Ser)
gnomAD v4
19g.1401422C=CA2317700449GAMTc.55G= (p.Ala19=)
19g.1401422C>GCA402998343GAMTc.55G>C (p.Ala19Pro)
dbSNP gnomAD v4
19g.1401422C>TCA402998344GAMTc.55G>A (p.Ala19Thr)
gnomAD v4
19g.1401422_1401423insACA2813256133GAMTc.54_55insT (p.Ala19CysfsTer?)
19g.1401423G>ACA304067345GAMTc.54C>T (p.Pro18=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.1401423G>CCA504731709GAMTc.54C>G (p.Pro18=)
ClinVar gnomAD v4
19g.1401423G=CA2317700450GAMTc.54C= (p.Pro18=)
19g.1401423G>TCA504731711GAMTc.54C>A (p.Pro18=)
gnomAD v4
19g.1401426dupCA2813256134GAMTc.54dup (p.Ala19ArgfsTer?)
19g.1401426delCA2582641927GAMTc.54del (p.Ala19ArgfsTer23)
c.54del (p.Ala19ArgfsTer?)
gnomAD v4
19g.1401424G>ACA402998345GAMTc.53C>T (p.Pro18Leu)
ClinVar dbSNP gnomAD v4
19g.1401424G>CCA402998347GAMTc.53C>G (p.Pro18Arg)
19g.1401424G>TCA402998348GAMTc.53C>A (p.Pro18His)
gnomAD v4
19g.1401425G>ACA402998350GAMTc.52C>T (p.Pro18Ser)
gnomAD v4
19g.1401425G>CCA402998351GAMTc.52C>G (p.Pro18Ala)
19g.1401425G>TCA402998352GAMTc.52C>A (p.Pro18Thr)
gnomAD v4
19g.1401426G>ACA504731717GAMTc.51C>T (p.Ser17=)
ClinVar dbSNP gnomAD v4
19g.1401426G>CCA402998354GAMTc.51C>G (p.Ser17Arg)
19g.1401426G=CA2317700451GAMTc.51C= (p.Ser17=)
19g.1401426G>TCA402998353GAMTc.51C>A (p.Ser17Arg)
dbSNP gnomAD v4
19g.1401427delCA2695198107GAMTc.50del (p.Ser17ThrfsTer25)
c.50del (p.Ser17ThrfsTer?)
ClinVar
19g.1401427C>ACA402998357GAMTc.50G>T (p.Ser17Ile)
gnomAD v4
19g.1401427C=CA2317700452GAMTc.50G= (p.Ser17=)
19g.1401427C>GCA402998358GAMTc.50G>C (p.Ser17Thr)
19g.1401427C>TCA304067348GAMTc.50G>A (p.Ser17Asn)
dbSNP gnomAD v3 gnomAD v4
19g.1401428T>ACA402998359GAMTc.49A>T (p.Ser17Cys)
19g.1401428T>CCA402998360GAMTc.49A>G (p.Ser17Gly)
gnomAD v4
19g.1401428T>GCA402998361GAMTc.49A>C (p.Ser17Arg)
gnomAD v4
19g.1401429G>ACA504731722GAMTc.48C>T (p.Cys16=)
gnomAD v4
19g.1401429G>CCA402998363GAMTc.48C>G (p.Cys16Trp)
gnomAD v4
19g.1401429G>TCA402998364GAMTc.48C>A (p.Cys16Ter)
ClinVar gnomAD v4
19g.1401430C>ACA402998365GAMTc.47G>T (p.Cys16Phe)
gnomAD v4
19g.1401430C=CA2317700453GAMTc.47G= (p.Cys16=)
19g.1401430C>GCA402998366GAMTc.47G>C (p.Cys16Ser)
gnomAD v4
19g.1401430C>TCA402998367GAMTc.47G>A (p.Cys16Tyr)
dbSNP gnomAD v2 gnomAD v4
19g.1401431A=CA2317700454GAMTc.46T= (p.Cys16=)
19g.1401431A>CCA402998372GAMTc.46T>G (p.Cys16Gly)
ClinVar dbSNP
19g.1401431A>GCA402998370GAMTc.46T>C (p.Cys16Arg)
gnomAD v4
19g.1401431A>TCA402998369GAMTc.46T>A (p.Cys16Ser)
gnomAD v4

Number of alleles fetched