Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.102851253_102856067delCA916084430PAHc.510-735_912+434del
c.495-735_897+434del
12g.102852716C=CA2059445788PAHc.842+99G= (p.=)
c.827+99G= (p.=)
n.601+99G=
n.3+99G=
12g.102852716C>TCA951235154PAHc.842+99G>A (p.=)
c.827+99G>A (p.=)
n.601+99G>A
n.3+99G>A
12g.102852718G>ACA242471474PAHc.842+97C>T (p.=)
c.827+97C>T (p.=)
n.601+97C>T
n.3+97C>T
dbSNP
12g.102852718G=CA2059445794PAHc.842+97C= (p.=)
c.827+97C= (p.=)
n.601+97C=
n.3+97C=
12g.102852719T>CCA951235156PAHc.842+96A>G (p.=)
c.827+96A>G (p.=)
n.601+96A>G
n.3+96A>G
12g.102852719T=CA2059445799PAHc.842+96A= (p.=)
c.827+96A= (p.=)
n.601+96A=
n.3+96A=
12g.102852721_102852736delinsGACCAGCCAGCAATGACA2059445807PAHc.842+79_842+94delinsTCATTGCTGGCTGGTC (p.=)
c.827+79_827+94delinsTCATTGCTGGCTGGTC (p.=)
n.601+79_601+94delinsTCATTGCTGGCTGGTC
n.3+79_3+94delinsTCATTGCTGGCTGGTC
12g.102852722A=CA2059445812PAHc.842+93T= (p.=)
c.827+93T= (p.=)
n.601+93T=
n.3+93T=
12g.102852722A>CCA2059445814PAHc.842+93T>G (p.=)
c.827+93T>G (p.=)
n.601+93T>G
n.3+93T>G
12g.102852725_102852739delCA242471475PAHc.842+79_842+93del (p.=)
c.827+79_827+93del (p.=)
n.601+79_601+93del
n.3+79_3+93del
dbSNP
12g.102852723C=CA2059445820PAHc.842+92G= (p.=)
c.827+92G= (p.=)
n.601+92G=
n.3+92G=
12g.102852723C>GCA242471478PAHc.842+92G>C (p.=)
c.827+92G>C (p.=)
n.601+92G>C
n.3+92G>C
dbSNP
12g.102852730G=CA2059445824PAHc.842+85C= (p.=)
c.827+85C= (p.=)
n.601+85C=
n.3+85C=
12g.102852730G>TCA682804812PAHc.842+85C>A (p.=)
c.827+85C>A (p.=)
n.601+85C>A
n.3+85C>A
12g.102852731C=CA2059445828PAHc.842+84G= (p.=)
c.827+84G= (p.=)
n.601+84G=
n.3+84G=
12g.102852731C>TCA2059445829PAHc.842+84G>A (p.=)
c.827+84G>A (p.=)
n.601+84G>A
n.3+84G>A
12g.102852735G>ACA2059445832PAHc.842+80C>T (p.=)
c.827+80C>T (p.=)
n.601+80C>T
n.3+80C>T
12g.102852735G=CA2059445830PAHc.842+80C= (p.=)
c.827+80C= (p.=)
n.601+80C=
n.3+80C=
12g.102852745C=CA2059445834PAHc.842+70G= (p.=)
c.827+70G= (p.=)
n.601+70G=
n.3+70G=
12g.102852745C>TCA2059445835PAHc.842+70G>A (p.=)
c.827+70G>A (p.=)
n.601+70G>A
n.3+70G>A
12g.102852747C=CA2059445837PAHc.842+68G= (p.=)
c.827+68G= (p.=)
n.601+68G=
n.3+68G=
12g.102852747C>TCA607154497PAHc.842+68G>A (p.=)
c.827+68G>A (p.=)
n.601+68G>A
n.3+68G>A
gnomAD
12g.102852751C=CA2059445839PAHc.842+64G= (p.=)
c.827+64G= (p.=)
n.601+64G=
n.3+64G=
12g.102852751C>GCA242471481PAHc.842+64G>C (p.=)
c.827+64G>C (p.=)
n.601+64G>C
n.3+64G>C
dbSNP
12g.102852753T>CCA951235164PAHc.842+62A>G (p.=)
c.827+62A>G (p.=)
n.601+62A>G
n.3+62A>G
12g.102852753T=CA2059445844PAHc.842+62A= (p.=)
c.827+62A= (p.=)
n.601+62A=
n.3+62A=
12g.102852754G>ACA2059445847PAHc.842+61C>T (p.=)
c.827+61C>T (p.=)
n.601+61C>T
n.3+61C>T
12g.102852754G=CA2059445846PAHc.842+61C= (p.=)
c.827+61C= (p.=)
n.601+61C=
n.3+61C=
12g.102852754G>TCA2059445848PAHc.842+61C>A (p.=)
c.827+61C>A (p.=)
n.601+61C>A
n.3+61C>A
12g.102852766G=CA2059445850PAHc.842+49C= (p.=)
c.827+49C= (p.=)
n.601+49C=
n.3+49C=
12g.102852766G>TCA6748825PAHc.842+49C>A (p.=)
c.827+49C>A (p.=)
n.601+49C>A
n.3+49C>A
dbSNP ExAC gnomAD
12g.102852767A=CA2059445854PAHc.842+48T= (p.=)
c.827+48T= (p.=)
n.601+48T=
n.3+48T=
12g.102852767A>GCA6748826PAHc.842+48T>C (p.=)
c.827+48T>C (p.=)
n.601+48T>C
n.3+48T>C
dbSNP ExAC gnomAD
12g.102852768T>CCA607154499PAHc.842+47A>G (p.=)
c.827+47A>G (p.=)
n.601+47A>G
n.3+47A>G
gnomAD
12g.102852768T=CA2059445858PAHc.842+47A= (p.=)
c.827+47A= (p.=)
n.601+47A=
n.3+47A=
12g.102852769G>ACA2059445866PAHc.842+46C>T (p.=)
c.827+46C>T (p.=)
n.601+46C>T
n.3+46C>T
12g.102852769G=CA2059445865PAHc.842+46C= (p.=)
c.827+46C= (p.=)
n.601+46C=
n.3+46C=
12g.102852771C=CA2059445872PAHc.842+44G= (p.=)
c.827+44G= (p.=)
n.601+44G=
n.3+44G=
12g.102852771C>TCA6748827PAHc.842+44G>A (p.=)
c.827+44G>A (p.=)
n.601+44G>A
n.3+44G>A
dbSNP ExAC gnomAD
12g.102852772G>ACA6748828PAHc.842+43C>T (p.=)
c.827+43C>T (p.=)
n.601+43C>T
n.3+43C>T
dbSNP ExAC gnomAD
12g.102852772G=CA2059445878PAHc.842+43C= (p.=)
c.827+43C= (p.=)
n.601+43C=
n.3+43C=
12g.102852773C=CA2059445882PAHc.842+42G= (p.=)
c.827+42G= (p.=)
n.601+42G=
n.3+42G=
12g.102852773C>TCA6748829PAHc.842+42G>A (p.=)
c.827+42G>A (p.=)
n.601+42G>A
n.3+42G>A
dbSNP ExAC gnomAD
12g.102852775C=CA2059445888PAHc.842+40G= (p.=)
c.827+40G= (p.=)
n.601+40G=
n.3+40G=
12g.102852775C>TCA6748830PAHc.842+40G>A (p.=)
c.827+40G>A (p.=)
n.601+40G>A
n.3+40G>A
dbSNP ExAC gnomAD
12g.102852782C=CA2059445893PAHc.842+33G= (p.=)
c.827+33G= (p.=)
n.601+33G=
n.3+33G=
12g.102852782C>TCA6748831PAHc.842+33G>A (p.=)
c.827+33G>A (p.=)
n.601+33G>A
n.3+33G>A
dbSNP ExAC gnomAD
12g.102852784T>GCA242471502PAHc.842+31A>C (p.=)
c.827+31A>C (p.=)
n.601+31A>C
n.3+31A>C
dbSNP gnomAD
12g.102852784T=CA2059445903PAHc.842+31A= (p.=)
c.827+31A= (p.=)
n.601+31A=
n.3+31A=

Number of alleles fetched