Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.73170815_73170831dupCA2146469616PSEN1c.106_122dup (p.Arg41SerfsTer?)
c.94_110dup (p.Arg37SerfsTer?)
c.-171_-155dup (n.-171_-155dup)
n.503_519dup
c.*50_*66dup (n.*50_*66dup)
dbSNP
14g.73170821_73170894delCA7256677PSEN1c.112_185del (p.His38GlyfsTer5)
c.100_173del (p.His34GlyfsTer5)
c.-165_-92del (n.-165_-92del)
c.100_173del (p.His34=)
c.*56_*129del (n.*56_*129del)
ExAC
14g.73170824A=CA2146469624PSEN1c.115A= (p.Asn39=)
c.103A= (p.Asn35=)
c.-162A= (n.-162A=)
n.512A=
c.*59A= (n.*59A=)
14g.73170824A>CCA390302530PSEN1c.115A>C (p.Asn39His)
c.103A>C (p.Asn35His)
c.-162A>C (n.-162A>C)
n.512A>C
c.*59A>C (n.*59A>C)
14g.73170824A>GCA390302531PSEN1c.115A>G (p.Asn39Asp)
c.103A>G (p.Asn35Asp)
c.-162A>G (n.-162A>G)
n.512A>G
c.*59A>G (n.*59A>G)
14g.73170824A>TCA390302532PSEN1c.115A>T (p.Asn39Tyr)
c.103A>T (p.Asn35Tyr)
c.-162A>T (n.-162A>T)
n.512A>T
c.*59A>T (n.*59A>T)
14g.73170824_73170827delinsAACGCA2146469623PSEN1c.115_118delinsAACG (p.Asn39=)
c.103_106delinsAACG (p.Asn35=)
c.-162_-159delinsAACG (n.-162_-159delinsAACG)
n.512_515delinsAACG
c.*59_*62delinsAACG (n.*59_*62delinsAACG)
14g.73170825A>CCA390302535PSEN1c.116A>C (p.Asn39Thr)
c.104A>C (p.Asn35Thr)
c.-161A>C (n.-161A>C)
n.513A>C
c.*60A>C (n.*60A>C)
14g.73170825A>GCA390302533PSEN1c.116A>G (p.Asn39Ser)
c.104A>G (p.Asn35Ser)
c.-161A>G (n.-161A>G)
n.513A>G
c.*60A>G (n.*60A>G)
14g.73170825A>TCA390302534PSEN1c.116A>T (p.Asn39Ile)
c.104A>T (p.Asn35Ile)
c.-161A>T (n.-161A>T)
n.513A>T
c.*60A>T (n.*60A>T)
14g.73170827_73170829delCA7256678PSEN1c.118_120del (p.Asp40del)
c.106_108del (p.Asp36del)
c.-159_-157del (n.-159_-157del)
n.515_517del
c.*62_*64del (n.*62_*64del)
ClinVar dbSNP ExAC gnomAD
14g.73170828_73170834dupCA615191109PSEN1c.119_125dup (p.Ser43GlnfsTer8)
c.107_113dup (p.Ser39GlnfsTer8)
c.-158_-152dup (n.-158_-152dup)
n.516_522dup
c.*63_*69dup (n.*63_*69dup)
dbSNP gnomAD
14g.73170826C>ACA390302536PSEN1c.117C>A (p.Asn39Lys)
c.105C>A (p.Asn35Lys)
c.-160C>A (n.-160C>A)
n.514C>A
c.*61C>A (n.*61C>A)
14g.73170826C=CA2146469625PSEN1c.117C= (p.Asn39=)
c.105C= (p.Asn35=)
c.-160C= (n.-160C=)
n.514C=
c.*61C= (n.*61C=)
14g.73170826C>GCA390302537PSEN1c.117C>G (p.Asn39Lys)
c.105C>G (p.Asn35Lys)
c.-160C>G (n.-160C>G)
n.514C>G
c.*61C>G (n.*61C>G)
14g.73170826C>TCA7256679PSEN1c.117C>T (p.Asn39=)
c.105C>T (p.Asn35=)
c.-160C>T (n.-160C>T)
n.514C>T
c.*61C>T (n.*61C>T)
dbSNP ExAC gnomAD
14g.73170827delCA2575570837PSEN1c.118del (p.Asp40ThrfsTer?)
c.106del (p.Asp36ThrfsTer?)
c.-159del (n.-159del)
n.515del
c.*62del (n.*62del)
14g.73170827G>ACA7256680PSEN1c.118G>A (p.Asp40Asn)
c.106G>A (p.Asp36Asn)
c.-159G>A (n.-159G>A)
n.515G>A
c.*62G>A (n.*62G>A)
dbSNP ExAC gnomAD
14g.73170827G>CCA390302539PSEN1c.118G>C (p.Asp40His)
c.106G>C (p.Asp36His)
c.-159G>C (n.-159G>C)
n.515G>C
c.*62G>C (n.*62G>C)
gnomAD
14g.73170827G=CA2146469626PSEN1c.118G= (p.Asp40=)
c.106G= (p.Asp36=)
c.-159G= (n.-159G=)
n.515G=
c.*62G= (n.*62G=)
14g.73170827G>TCA390302538PSEN1c.118G>T (p.Asp40Tyr)
c.106G>T (p.Asp36Tyr)
c.-159G>T (n.-159G>T)
n.515G>T
c.*62G>T (n.*62G>T)
14g.73170828A=CA2146469627PSEN1c.119A= (p.Asp40=)
c.107A= (p.Asp36=)
c.-158A= (n.-158A=)
n.516A=
c.*63A= (n.*63A=)
14g.73170828A>CCA390302540PSEN1c.119A>C (p.Asp40Ala)
c.107A>C (p.Asp36Ala)
c.-158A>C (n.-158A>C)
n.516A>C
c.*63A>C (n.*63A>C)
14g.73170828A>GCA390302541PSEN1c.119A>G (p.Asp40Gly)
c.107A>G (p.Asp36Gly)
c.-158A>G (n.-158A>G)
n.516A>G
c.*63A>G (n.*63A>G)
14g.73170828A>TCA390302542PSEN1c.119A>T (p.Asp40Val)
c.107A>T (p.Asp36Val)
c.-158A>T (n.-158A>T)
n.516A>T
c.*63A>T (n.*63A>T)
14g.73170828_73170833dupCA2146469628PSEN1c.119_124dup (p.Arg41_Arg42insHisArg)
c.107_112dup (p.Arg37_Arg38insHisArg)
c.-158_-153dup (n.-158_-153dup)
n.516_521dup
c.*63_*68dup (n.*63_*68dup)
dbSNP
14g.73170829C>ACA390302543PSEN1c.120C>A (p.Asp40Glu)
c.108C>A (p.Asp36Glu)
c.-157C>A (n.-157C>A)
n.517C>A
c.*64C>A (n.*64C>A)
14g.73170829C=CA2146469629PSEN1c.120C= (p.Asp40=)
c.108C= (p.Asp36=)
c.-157C= (n.-157C=)
n.517C=
c.*64C= (n.*64C=)
14g.73170829C>GCA390302544PSEN1c.120C>G (p.Asp40Glu)
c.108C>G (p.Asp36Glu)
c.-157C>G (n.-157C>G)
n.517C>G
c.*64C>G (n.*64C>G)
14g.73170829C>TCA487255432PSEN1c.120C>T (p.Asp40=)
c.108C>T (p.Asp36=)
c.-157C>T (n.-157C>T)
n.517C>T
c.*64C>T (n.*64C>T)
14g.73170830_73170831insCCTTGGCCACA708405983PSEN1c.121_122insCCTTGGCCA (p.Asp40_Arg41insThrLeuAla)
c.109_110insCCTTGGCCA (p.Asp36_Arg37insThrLeuAla)
c.-156_-155insCCTTGGCCA (n.-156_-155insCCTTGGCCA)
n.518_519insCCTTGGCCA
c.*65_*66insCCTTGGCCA (n.*65_*66insCCTTGGCCA)
dbSNP
14g.73170830A=CA2146469630PSEN1c.121A= (p.Arg41=)
c.109A= (p.Arg37=)
c.-156A= (n.-156A=)
n.518A=
c.*65A= (n.*65A=)
14g.73170830A>CCA487255433PSEN1c.121A>C (p.Arg41=)
c.109A>C (p.Arg37=)
c.-156A>C (n.-156A>C)
n.518A>C
c.*65A>C (n.*65A>C)
gnomAD
14g.73170830A>GCA390302545PSEN1c.121A>G (p.Arg41Gly)
c.109A>G (p.Arg37Gly)
c.-156A>G (n.-156A>G)
n.518A>G
c.*65A>G (n.*65A>G)
gnomAD
14g.73170830A>TCA390302546PSEN1c.121A>T (p.Arg41Ter)
c.109A>T (p.Arg37Ter)
c.-156A>T (n.-156A>T)
n.518A>T
c.*65A>T (n.*65A>T)
14g.73170830_73170831insCCTTCA7256681PSEN1c.121_122insCCTT (p.Arg41ThrfsTer9)
c.109_110insCCTT (p.Arg37ThrfsTer9)
c.-156_-155insCCTT (n.-156_-155insCCTT)
n.518_519insCCTT
c.*65_*66insCCTT (n.*65_*66insCCTT)
dbSNP ExAC gnomAD
14g.73170831G>ACA390302547PSEN1c.122G>A (p.Arg41Lys)
c.110G>A (p.Arg37Lys)
c.-155G>A (n.-155G>A)
n.519G>A
c.*66G>A (n.*66G>A)
14g.73170831G>CCA262614369PSEN1c.122G>C (p.Arg41Thr)
c.110G>C (p.Arg37Thr)
c.-155G>C (n.-155G>C)
n.519G>C
c.*66G>C (n.*66G>C)
dbSNP
14g.73170831G=CA2146469631PSEN1c.122G= (p.Arg41=)
c.110G= (p.Arg37=)
c.-155G= (n.-155G=)
n.519G=
c.*66G= (n.*66G=)
14g.73170831G>TCA390302548PSEN1c.122G>T (p.Arg41Ile)
c.110G>T (p.Arg37Ile)
c.-155G>T (n.-155G>T)
n.519G>T
c.*66G>T (n.*66G>T)
14g.73170831_73170837delCA2575570838PSEN1c.122_128del (p.Arg41ThrfsTer?)
c.110_116del (p.Arg37ThrfsTer?)
c.-155_-149del (n.-155_-149del)
n.519_525del
c.*66_*72del (n.*66_*72del)
14g.73170831_73170832insGCCCA7256682PSEN1c.122_123insGCC (p.Arg41_Arg42insPro)
c.110_111insGCC (p.Arg37_Arg38insPro)
c.-155_-154insGCC (n.-155_-154insGCC)
n.519_520insGCC
c.*66_*67insGCC (n.*66_*67insGCC)
dbSNP ExAC gnomAD
14g.73170832A=CA2146469632PSEN1c.123A= (p.Arg41=)
c.111A= (p.Arg37=)
c.-154A= (n.-154A=)
n.520A=
c.*67A= (n.*67A=)
14g.73170832A>CCA262614373PSEN1c.123A>C (p.Arg41Ser)
c.111A>C (p.Arg37Ser)
c.-154A>C (n.-154A>C)
n.520A>C
c.*67A>C (n.*67A>C)
dbSNP
14g.73170832A>GCA487255438PSEN1c.123A>G (p.Arg41=)
c.111A>G (p.Arg37=)
c.-154A>G (n.-154A>G)
n.520A>G
c.*67A>G (n.*67A>G)
14g.73170832A>TCA390302549PSEN1c.123A>T (p.Arg41Ser)
c.111A>T (p.Arg37Ser)
c.-154A>T (n.-154A>T)
n.520A>T
c.*67A>T (n.*67A>T)
ClinVar
14g.73170833C>ACA487255442PSEN1c.124C>A (p.Arg42=)
c.112C>A (p.Arg38=)
c.-153C>A (n.-153C>A)
n.521C>A
c.*68C>A (n.*68C>A)
14g.73170833C=CA2146469633PSEN1c.124C= (p.Arg42=)
c.112C= (p.Arg38=)
c.-153C= (n.-153C=)
n.521C=
c.*68C= (n.*68C=)
14g.73170833C>GCA7256685PSEN1c.124C>G (p.Arg42Gly)
c.112C>G (p.Arg38Gly)
c.-153C>G (n.-153C>G)
n.521C>G
c.*68C>G (n.*68C>G)
ClinVar dbSNP ExAC gnomAD
14g.73170833C>TCA7256684PSEN1c.124C>T (p.Arg42Trp)
c.112C>T (p.Arg38Trp)
c.-153C>T (n.-153C>T)
n.521C>T
c.*68C>T (n.*68C>T)
dbSNP ExAC gnomAD COSMIC COSMIC

Number of alleles fetched