Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.92517348_92518796delCA916082939PEX1c.357+202_1170del
n.357+202_1170del
c.273+3309_274-3378del (p.=)
n.396+167_1209del
c.-268+167_546del
n.453+202_1266del
n.404+202_1217del
ClinVar
7g.92518256C>ACA16041173PEX1c.358-1G>T (p.=)
n.358-1G>T (p.=)
c.273+3846G>T (p.=)
n.397-1G>T
c.-267-1G>T (p.=)
n.454-1G>T
n.405-1G>T
ClinVar dbSNP
7g.92518256C=CA1725948598PEX1c.358-1G= (p.=)
n.358-1G= (p.=)
c.273+3846G= (p.=)
n.397-1G=
c.-267-1G= (p.=)
n.454-1G=
n.405-1G=
7g.92518256C>GCA368202688PEX1c.358-1G>C (p.=)
n.358-1G>C (p.=)
c.273+3846G>C (p.=)
n.397-1G>C
c.-267-1G>C (p.=)
n.454-1G>C
n.405-1G>C
7g.92518256C>TCA368202690PEX1c.358-1G>A (p.=)
n.358-1G>A (p.=)
c.273+3846G>A (p.=)
n.397-1G>A
c.-267-1G>A (p.=)
n.454-1G>A
n.405-1G>A
COSMIC
7g.92518257T>ACA368202692PEX1c.358-2A>T (p.=)
n.358-2A>T (p.=)
c.273+3845A>T (p.=)
n.397-2A>T
c.-267-2A>T (p.=)
n.454-2A>T
n.405-2A>T
7g.92518257T>CCA16041174PEX1c.358-2A>G (p.=)
n.358-2A>G (p.=)
c.273+3845A>G (p.=)
n.397-2A>G
c.-267-2A>G (p.=)
n.454-2A>G
n.405-2A>G
ClinVar dbSNP gnomAD
7g.92518257T>GCA368202694PEX1c.358-2A>C (p.=)
n.358-2A>C (p.=)
c.273+3845A>C (p.=)
n.397-2A>C
c.-267-2A>C (p.=)
n.454-2A>C
n.405-2A>C
ClinVar
7g.92518257T=CA1725948604PEX1c.358-2A= (p.=)
n.358-2A= (p.=)
c.273+3845A= (p.=)
n.397-2A=
c.-267-2A= (p.=)
n.454-2A=
n.405-2A=
7g.92518261A=CA1725948612PEX1c.358-6T= (p.=)
n.358-6T= (p.=)
c.273+3841T= (p.=)
n.397-6T=
c.-267-6T= (p.=)
n.454-6T=
n.405-6T=
7g.92518261A>GCA1725948614PEX1c.358-6T>C (p.=)
n.358-6T>C (p.=)
c.273+3841T>C (p.=)
n.397-6T>C
c.-267-6T>C (p.=)
n.454-6T>C
n.405-6T>C
7g.92518262C>ACA843847229PEX1c.358-7G>T (p.=)
n.358-7G>T (p.=)
c.273+3840G>T (p.=)
n.397-7G>T
c.-267-7G>T (p.=)
n.454-7G>T
n.405-7G>T
7g.92518262C=CA1725948615PEX1c.358-7G= (p.=)
n.358-7G= (p.=)
c.273+3840G= (p.=)
n.397-7G=
c.-267-7G= (p.=)
n.454-7G=
n.405-7G=
7g.92518263C>ACA1104477094PEX1c.358-8G>T (p.=)
n.358-8G>T (p.=)
c.273+3839G>T (p.=)
n.397-8G>T
c.-267-8G>T (p.=)
n.454-8G>T
n.405-8G>T
7g.92518263C=CA1725948616PEX1c.358-8G= (p.=)
n.358-8G= (p.=)
c.273+3839G= (p.=)
n.397-8G=
c.-267-8G= (p.=)
n.454-8G=
n.405-8G=
7g.92518263C>GCA1725948618PEX1c.358-8G>C (p.=)
n.358-8G>C (p.=)
c.273+3839G>C (p.=)
n.397-8G>C
c.-267-8G>C (p.=)
n.454-8G>C
n.405-8G>C
ClinVar
7g.92518266C>ACA4341617PEX1c.358-11G>T (p.=)
n.358-11G>T (p.=)
c.273+3836G>T (p.=)
n.397-11G>T
c.-267-11G>T (p.=)
n.454-11G>T
n.405-11G>T
dbSNP ExAC gnomAD
7g.92518266C=CA1725948623PEX1c.358-11G= (p.=)
n.358-11G= (p.=)
c.273+3836G= (p.=)
n.397-11G=
c.-267-11G= (p.=)
n.454-11G=
n.405-11G=
7g.92518266C>GCA4341616PEX1c.358-11G>C (p.=)
n.358-11G>C (p.=)
c.273+3836G>C (p.=)
n.397-11G>C
c.-267-11G>C (p.=)
n.454-11G>C
n.405-11G>C
ClinVar dbSNP ExAC gnomAD
7g.92518268G>ACA4341618PEX1c.358-13C>T (p.=)
n.358-13C>T (p.=)
c.273+3834C>T (p.=)
n.397-13C>T
c.-267-13C>T (p.=)
n.454-13C>T
n.405-13C>T
dbSNP ExAC gnomAD
7g.92518268G>CCA161974197PEX1c.358-13C>G (p.=)
n.358-13C>G (p.=)
c.273+3834C>G (p.=)
n.397-13C>G
c.-267-13C>G (p.=)
n.454-13C>G
n.405-13C>G
dbSNP gnomAD
7g.92518268G=CA1725948633PEX1c.358-13C= (p.=)
n.358-13C= (p.=)
c.273+3834C= (p.=)
n.397-13C=
c.-267-13C= (p.=)
n.454-13C=
n.405-13C=
7g.92518268_92518272delinsGACGACA1725948630PEX1c.358-17_358-13delinsTCGTC (p.=)
n.358-17_358-13delinsTCGTC (p.=)
c.273+3830_273+3834delinsTCGTC (p.=)
n.397-17_397-13delinsTCGTC
c.-267-17_-267-13delinsTCGTC (p.=)
n.454-17_454-13delinsTCGTC
n.405-17_405-13delinsTCGTC
7g.92518268_92518274delinsGACGAAACA1725948631PEX1c.358-19_358-13delinsTTTCGTC (p.=)
n.358-19_358-13delinsTTTCGTC (p.=)
c.273+3828_273+3834delinsTTTCGTC (p.=)
n.397-19_397-13delinsTTTCGTC
c.-267-19_-267-13delinsTTTCGTC (p.=)
n.454-19_454-13delinsTTTCGTC
n.405-19_405-13delinsTTTCGTC
7g.92518270_92518273delCA843847243PEX1c.358-17_358-14del (p.=)
n.358-17_358-14del (p.=)
c.273+3830_273+3833del (p.=)
n.397-17_397-14del
c.-267-17_-267-14del (p.=)
n.454-17_454-14del
n.405-17_405-14del
dbSNP
7g.92518270_92518275delCA576308159PEX1c.358-19_358-14del (p.=)
n.358-19_358-14del (p.=)
c.273+3828_273+3833del (p.=)
n.397-19_397-14del
c.-267-19_-267-14del (p.=)
n.454-19_454-14del
n.405-19_405-14del
dbSNP gnomAD
7g.92518270C=CA1725948647PEX1c.358-15G= (p.=)
n.358-15G= (p.=)
c.273+3832G= (p.=)
n.397-15G=
c.-267-15G= (p.=)
n.454-15G=
n.405-15G=
7g.92518270C>TCA146665PEX1c.358-15G>A (p.=)
n.358-15G>A (p.=)
c.273+3832G>A (p.=)
n.397-15G>A
c.-267-15G>A (p.=)
n.454-15G>A
n.405-15G>A
ClinVar dbSNP ExAC gnomAD
7g.92518270_92518271insATCTTGGGCA2566347344PEX1c.358-16_358-15insCCCAAGAT (p.=)
n.358-16_358-15insCCCAAGAT (p.=)
c.273+3831_273+3832insCCCAAGAT (p.=)
n.397-16_397-15insCCCAAGAT
c.-267-16_-267-15insCCCAAGAT (p.=)
n.454-16_454-15insCCCAAGAT
n.405-16_405-15insCCCAAGAT
7g.92518271G>ACA2557735552PEX1c.358-16C>T (p.=)
n.358-16C>T (p.=)
c.273+3831C>T (p.=)
n.397-16C>T
c.-267-16C>T (p.=)
n.454-16C>T
n.405-16C>T
7g.92518274A=CA1725948650PEX1c.358-19T= (p.=)
n.358-19T= (p.=)
c.273+3828T= (p.=)
n.397-19T=
c.-267-19T= (p.=)
n.454-19T=
n.405-19T=
7g.92518274A>TCA161974198PEX1c.358-19T>A (p.=)
n.358-19T>A (p.=)
c.273+3828T>A (p.=)
n.397-19T>A
c.-267-19T>A (p.=)
n.454-19T>A
n.405-19T>A
dbSNP
7g.92518275A=CA1725948653PEX1c.358-20T= (p.=)
n.358-20T= (p.=)
c.273+3827T= (p.=)
n.397-20T=
c.-267-20T= (p.=)
n.454-20T=
n.405-20T=
7g.92518275A>TCA161974201PEX1c.358-20T>A (p.=)
n.358-20T>A (p.=)
c.273+3827T>A (p.=)
n.397-20T>A
c.-267-20T>A (p.=)
n.454-20T>A
n.405-20T>A
dbSNP
7g.92518275_92518276insTTCA576308160PEX1c.358-21_358-20insAA (p.=)
n.358-21_358-20insAA (p.=)
c.273+3826_273+3827insAA (p.=)
n.397-21_397-20insAA
c.-267-21_-267-20insAA (p.=)
n.454-21_454-20insAA
n.405-21_405-20insAA
dbSNP gnomAD
7g.92518279C>GCA2551485338PEX1c.358-24G>C (p.=)
n.358-24G>C (p.=)
c.273+3823G>C (p.=)
n.397-24G>C
c.-267-24G>C (p.=)
n.454-24G>C
n.405-24G>C
7g.92518281A=CA1725948656PEX1c.358-26T= (p.=)
n.358-26T= (p.=)
c.273+3821T= (p.=)
n.397-26T=
c.-267-26T= (p.=)
n.454-26T=
n.405-26T=
7g.92518281A>GCA4341619PEX1c.358-26T>C (p.=)
n.358-26T>C (p.=)
c.273+3821T>C (p.=)
n.397-26T>C
c.-267-26T>C (p.=)
n.454-26T>C
n.405-26T>C
dbSNP ExAC gnomAD
7g.92518282T>CCA1725948660PEX1c.358-27A>G (p.=)
n.358-27A>G (p.=)
c.273+3820A>G (p.=)
n.397-27A>G
c.-267-27A>G (p.=)
n.454-27A>G
n.405-27A>G
7g.92518282T=CA1725948659PEX1c.358-27A= (p.=)
n.358-27A= (p.=)
c.273+3820A= (p.=)
n.397-27A=
c.-267-27A= (p.=)
n.454-27A=
n.405-27A=
7g.92518282_92518283insGTTGCTTTGGAGAAAGTAGCTCA4341620PEX1c.358-27_358-26insGCTACTTTCTCCAAAGCAACA (p.=)
n.358-27_358-26insGCTACTTTCTCCAAAGCAACA (p.=)
c.273+3820_273+3821insGCTACTTTCTCCAAAGCAACA (p.=)
n.397-27_397-26insGCTACTTTCTCCAAAGCAACA
c.-267-27_-267-26insGCTACTTTCTCCAAAGCAACA (p.=)
n.454-27_454-26insGCTACTTTCTCCAAAGCAACA
n.405-27_405-26insGCTACTTTCTCCAAAGCAACA
dbSNP ExAC
7g.92518284C>ACA4341621PEX1c.358-29G>T (p.=)
n.358-29G>T (p.=)
c.273+3818G>T (p.=)
n.397-29G>T
c.-267-29G>T (p.=)
n.454-29G>T
n.405-29G>T
dbSNP ExAC
7g.92518284C=CA1725948664PEX1c.358-29G= (p.=)
n.358-29G= (p.=)
c.273+3818G= (p.=)
n.397-29G=
c.-267-29G= (p.=)
n.454-29G=
n.405-29G=
7g.92518284C>TCA843847258PEX1c.358-29G>A (p.=)
n.358-29G>A (p.=)
c.273+3818G>A (p.=)
n.397-29G>A
c.-267-29G>A (p.=)
n.454-29G>A
n.405-29G>A
7g.92518289T>ACA843847260PEX1c.358-34A>T (p.=)
n.358-34A>T (p.=)
c.273+3813A>T (p.=)
n.397-34A>T
c.-267-34A>T (p.=)
n.454-34A>T
n.405-34A>T
7g.92518289T>GCA2548292083PEX1c.358-34A>C (p.=)
n.358-34A>C (p.=)
c.273+3813A>C (p.=)
n.397-34A>C
c.-267-34A>C (p.=)
n.454-34A>C
n.405-34A>C
7g.92518289T=CA1725948665PEX1c.358-34A= (p.=)
n.358-34A= (p.=)
c.273+3813A= (p.=)
n.397-34A=
c.-267-34A= (p.=)
n.454-34A=
n.405-34A=
7g.92518291C=CA1725948666PEX1c.358-36G= (p.=)
n.358-36G= (p.=)
c.273+3811G= (p.=)
n.397-36G=
c.-267-36G= (p.=)
n.454-36G=
n.405-36G=
7g.92518291C>TCA4341622PEX1c.358-36G>A (p.=)
n.358-36G>A (p.=)
c.273+3811G>A (p.=)
n.397-36G>A
c.-267-36G>A (p.=)
n.454-36G>A
n.405-36G>A
dbSNP ExAC gnomAD
7g.92518299C>TCA2536831610PEX1c.358-44G>A (p.=)
n.358-44G>A (p.=)
c.273+3803G>A (p.=)
n.397-44G>A
c.-267-44G>A (p.=)
n.454-44G>A
n.405-44G>A

Number of alleles fetched