Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.73170940T>ACA390303094PSEN1c.231T>A (p.Tyr77Ter)
c.219T>A (p.Tyr73Ter)
c.-46T>A (n.-46T>A)
c.*175T>A (n.*175T>A)
14g.73170940T>CCA487255788PSEN1c.231T>C (p.Tyr77=)
c.219T>C (p.Tyr73=)
c.-46T>C (n.-46T>C)
c.*175T>C (n.*175T>C)
gnomAD
14g.73170940T>GCA390303096PSEN1c.231T>G (p.Tyr77Ter)
c.219T>G (p.Tyr73Ter)
c.-46T>G (n.-46T>G)
c.*175T>G (n.*175T>G)
14g.73170940T=CA2146469684PSEN1c.231T= (p.Tyr77=)
c.219T= (p.Tyr73=)
c.-46T= (n.-46T=)
c.*175T= (n.*175T=)
14g.73170941G>ACA390303106PSEN1c.232G>A (p.Gly78Ser)
c.220G>A (p.Gly74Ser)
c.-45G>A (n.-45G>A)
c.*176G>A (n.*176G>A)
14g.73170941G>CCA390303103PSEN1c.232G>C (p.Gly78Arg)
c.220G>C (p.Gly74Arg)
c.-45G>C (n.-45G>C)
c.*176G>C (n.*176G>C)
14g.73170941G>TCA390303101PSEN1c.232G>T (p.Gly78Cys)
c.220G>T (p.Gly74Cys)
c.-45G>T (n.-45G>T)
c.*176G>T (n.*176G>T)
14g.73170942G>ACA390303114PSEN1c.233G>A (p.Gly78Asp)
c.221G>A (p.Gly74Asp)
c.-44G>A (n.-44G>A)
c.*177G>A (n.*177G>A)
COSMIC COSMIC
14g.73170942G>CCA390303109PSEN1c.233G>C (p.Gly78Ala)
c.221G>C (p.Gly74Ala)
c.-44G>C (n.-44G>C)
c.*177G>C (n.*177G>C)
14g.73170942G>TCA390303112PSEN1c.233G>T (p.Gly78Val)
c.221G>T (p.Gly74Val)
c.-44G>T (n.-44G>T)
c.*177G>T (n.*177G>T)
14g.73170943C>ACA487255790PSEN1c.234C>A (p.Gly78=)
c.222C>A (p.Gly74=)
c.-43C>A (n.-43C>A)
c.*178C>A (n.*178C>A)
ClinVar
14g.73170943C=CA2146469685PSEN1c.234C= (p.Gly78=)
c.222C= (p.Gly74=)
c.-43C= (n.-43C=)
c.*178C= (n.*178C=)
14g.73170943C>GCA487255791PSEN1c.234C>G (p.Gly78=)
c.222C>G (p.Gly74=)
c.-43C>G (n.-43C>G)
c.*178C>G (n.*178C>G)
14g.73170943C>TCA7256698PSEN1c.234C>T (p.Gly78=)
c.222C>T (p.Gly74=)
c.-43C>T (n.-43C>T)
c.*178C>T (n.*178C>T)
ClinVar dbSNP ExAC gnomAD
14g.73170944G>ACA7256699PSEN1c.235G>A (p.Ala79Thr)
c.223G>A (p.Ala75Thr)
c.-42G>A (n.-42G>A)
c.*179G>A (n.*179G>A)
dbSNP ExAC gnomAD
14g.73170944G>CCA390303121PSEN1c.235G>C (p.Ala79Pro)
c.223G>C (p.Ala75Pro)
c.-42G>C (n.-42G>C)
c.*179G>C (n.*179G>C)
14g.73170944G=CA2146469686PSEN1c.235G= (p.Ala79=)
c.223G= (p.Ala75=)
c.-42G= (n.-42G=)
c.*179G= (n.*179G=)
14g.73170944G>TCA390303123PSEN1c.235G>T (p.Ala79Ser)
c.223G>T (p.Ala75Ser)
c.-42G>T (n.-42G>T)
c.*179G>T (n.*179G>T)
14g.73170945C>ACA390303131PSEN1c.236C>A (p.Ala79Asp)
c.224C>A (p.Ala75Asp)
c.-41C>A (n.-41C>A)
c.*180C>A (n.*180C>A)
14g.73170945C=CA2146469687PSEN1c.236C= (p.Ala79=)
c.224C= (p.Ala75=)
c.-41C= (n.-41C=)
c.*180C= (n.*180C=)
14g.73170945C>GCA390303129PSEN1c.236C>G (p.Ala79Gly)
c.224C>G (p.Ala75Gly)
c.-41C>G (n.-41C>G)
c.*180C>G (n.*180C>G)
gnomAD
14g.73170945C>TCA224983PSEN1c.236C>T (p.Ala79Val)
c.224C>T (p.Ala75Val)
c.-41C>T (n.-41C>T)
c.*180C>T (n.*180C>T)
ClinVar dbSNP ExAC gnomAD
14g.73170946C>ACA487255796PSEN1c.237C>A (p.Ala79=)
c.225C>A (p.Ala75=)
c.-40C>A (n.-40C>A)
c.*181C>A (n.*181C>A)
14g.73170946C>GCA487255797PSEN1c.237C>G (p.Ala79=)
c.225C>G (p.Ala75=)
c.-40C>G (n.-40C>G)
c.*181C>G (n.*181C>G)
14g.73170946C>TCA487255798PSEN1c.237C>T (p.Ala79=)
c.225C>T (p.Ala75=)
c.-40C>T (n.-40C>T)
c.*181C>T (n.*181C>T)
14g.73170947A>CCA390303133PSEN1c.238A>C (p.Lys80Gln)
c.226A>C (p.Lys76Gln)
c.-39A>C (n.-39A>C)
c.*182A>C (n.*182A>C)
14g.73170947A>GCA390303136PSEN1c.238A>G (p.Lys80Glu)
c.226A>G (p.Lys76Glu)
c.-39A>G (n.-39A>G)
c.*182A>G (n.*182A>G)
14g.73170947A>TCA390303138PSEN1c.238A>T (p.Lys80Ter)
c.226A>T (p.Lys76Ter)
c.-39A>T (n.-39A>T)
c.*182A>T (n.*182A>T)
14g.73170948A=CA2146469688PSEN1c.239A= (p.Lys80=)
c.227A= (p.Lys76=)
c.-38A= (n.-38A=)
c.*183A= (n.*183A=)
14g.73170948A>CCA390303142PSEN1c.239A>C (p.Lys80Thr)
c.227A>C (p.Lys76Thr)
c.-38A>C (n.-38A>C)
c.*183A>C (n.*183A>C)
14g.73170948A>GCA390303144PSEN1c.239A>G (p.Lys80Arg)
c.227A>G (p.Lys76Arg)
c.-38A>G (n.-38A>G)
c.*183A>G (n.*183A>G)
gnomAD
14g.73170948A>TCA390303145PSEN1c.239A>T (p.Lys80Met)
c.227A>T (p.Lys76Met)
c.-38A>T (n.-38A>T)
c.*183A>T (n.*183A>T)
14g.73170949G>ACA262614430PSEN1c.240G>A (p.Lys80=)
c.228G>A (p.Lys76=)
c.-37G>A (n.-37G>A)
c.*184G>A (n.*184G>A)
dbSNP gnomAD
14g.73170949G>CCA390303152PSEN1c.240G>C (p.Lys80Asn)
c.228G>C (p.Lys76Asn)
c.-37G>C (n.-37G>C)
c.*184G>C (n.*184G>C)
14g.73170949G=CA2146469689PSEN1c.240G= (p.Lys80=)
c.228G= (p.Lys76=)
c.-37G= (n.-37G=)
c.*184G= (n.*184G=)
14g.73170949G>TCA390303150PSEN1c.240G>T (p.Lys80Asn)
c.228G>T (p.Lys76Asn)
c.-37G>T (n.-37G>T)
c.*184G>T (n.*184G>T)
14g.73170950C>ACA390303157PSEN1c.241C>A (p.His81Asn)
c.229C>A (p.His77Asn)
c.-36C>A (n.-36C>A)
c.*185C>A (n.*185C>A)
14g.73170950C>GCA390303159PSEN1c.241C>G (p.His81Asp)
c.229C>G (p.His77Asp)
c.-36C>G (n.-36C>G)
c.*185C>G (n.*185C>G)
14g.73170950C>TCA390303161PSEN1c.241C>T (p.His81Tyr)
c.229C>T (p.His77Tyr)
c.-36C>T (n.-36C>T)
c.*185C>T (n.*185C>T)
COSMIC COSMIC COSMIC
14g.73170951A>CCA390303164PSEN1c.242A>C (p.His81Pro)
c.230A>C (p.His77Pro)
c.-35A>C (n.-35A>C)
c.*186A>C (n.*186A>C)
14g.73170951A>GCA390303166PSEN1c.242A>G (p.His81Arg)
c.230A>G (p.His77Arg)
c.-35A>G (n.-35A>G)
c.*186A>G (n.*186A>G)
14g.73170951A>TCA390303168PSEN1c.242A>T (p.His81Leu)
c.230A>T (p.His77Leu)
c.-35A>T (n.-35A>T)
c.*186A>T (n.*186A>T)
14g.73170951_73170954dupCA2575570840PSEN1c.242_245dup (p.Ile83CysfsTer20)
c.230_233dup (p.Ile79CysfsTer20)
c.-35_-32dup (n.-35_-32dup)
c.230_233dup (p.Ile79CysfsTer?)
c.242_245dup (p.Ile83CysfsTer?)
c.*186_*189dup (n.*186_*189dup)
14g.73170952T>ACA390303171PSEN1c.243T>A (p.His81Gln)
c.231T>A (p.His77Gln)
c.-34T>A (n.-34T>A)
c.*187T>A (n.*187T>A)
14g.73170952T>CCA262614432PSEN1c.243T>C (p.His81=)
c.231T>C (p.His77=)
c.-34T>C (n.-34T>C)
c.*187T>C (n.*187T>C)
dbSNP gnomAD
14g.73170952T>GCA390303175PSEN1c.243T>G (p.His81Gln)
c.231T>G (p.His77Gln)
c.-34T>G (n.-34T>G)
c.*187T>G (n.*187T>G)
14g.73170952T=CA2146469690PSEN1c.243T= (p.His81=)
c.231T= (p.His77=)
c.-34T= (n.-34T=)
c.*187T= (n.*187T=)
14g.73170953G>ACA390303178PSEN1c.244G>A (p.Val82Met)
c.232G>A (p.Val78Met)
c.-33G>A (n.-33G>A)
c.*188G>A (n.*188G>A)
14g.73170953G>CCA224984PSEN1c.244G>C (p.Val82Leu)
c.232G>C (p.Val78Leu)
c.-33G>C (n.-33G>C)
c.*188G>C (n.*188G>C)
ClinVar dbSNP
14g.73170953G=CA2146469691PSEN1c.244G= (p.Val82=)
c.232G= (p.Val78=)
c.-33G= (n.-33G=)
c.*188G= (n.*188G=)

Number of alleles fetched