Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.43122738A=CA1779747939POMKc.914A= (p.His305=)
c.*710A= (n.*710A=)
c.632A= (p.His211=)
c.*834A= (n.*834A=)
c.872A= (p.His291=)
c.*699A= (n.*699A=)
8g.43122738A>CCA371122951POMKc.914A>C (p.His305Pro)
c.*710A>C (n.*710A>C)
c.632A>C (p.His211Pro)
c.*834A>C (n.*834A>C)
c.872A>C (p.His291Pro)
c.*699A>C (n.*699A>C)
8g.43122738A>GCA4736378POMKc.914A>G (p.His305Arg)
c.*710A>G (n.*710A>G)
c.632A>G (p.His211Arg)
c.*834A>G (n.*834A>G)
c.872A>G (p.His291Arg)
c.*699A>G (n.*699A>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.43122738A>TCA371122952POMKc.914A>T (p.His305Leu)
c.*710A>T (n.*710A>T)
c.632A>T (p.His211Leu)
c.*834A>T (n.*834A>T)
c.872A>T (p.His291Leu)
c.*699A>T (n.*699A>T)
8g.43122739T>ACA371122953POMKc.915T>A (p.His305Gln)
c.*711T>A (n.*711T>A)
c.633T>A (p.His211Gln)
c.*835T>A (n.*835T>A)
c.873T>A (p.His291Gln)
c.*700T>A (n.*700T>A)
8g.43122739T>CCA460787441POMKc.915T>C (p.His305=)
c.*711T>C (n.*711T>C)
c.633T>C (p.His211=)
c.*835T>C (n.*835T>C)
c.873T>C (p.His291=)
c.*700T>C (n.*700T>C)
8g.43122739T>GCA371122954POMKc.915T>G (p.His305Gln)
c.*711T>G (n.*711T>G)
c.633T>G (p.His211Gln)
c.*835T>G (n.*835T>G)
c.873T>G (p.His291Gln)
c.*700T>G (n.*700T>G)
8g.43122741dupCA10603099POMKc.917dup (p.Leu306PhefsTer3)
c.*713dup (n.*713dup)
c.635dup (p.Leu212PhefsTer3)
c.*837dup (n.*837dup)
c.875dup (p.Leu292PhefsTer3)
c.*702dup (n.*702dup)
ClinVar dbSNP
8g.43122740T>ACA371122955POMKc.916T>A (p.Leu306Met)
c.*712T>A (n.*712T>A)
c.634T>A (p.Leu212Met)
c.*836T>A (n.*836T>A)
c.874T>A (p.Leu292Met)
c.*701T>A (n.*701T>A)
8g.43122740T>CCA460787442POMKc.916T>C (p.Leu306=)
c.*712T>C (n.*712T>C)
c.634T>C (p.Leu212=)
c.*836T>C (n.*836T>C)
c.874T>C (p.Leu292=)
c.*701T>C (n.*701T>C)
8g.43122740T>GCA371122956POMKc.916T>G (p.Leu306Val)
c.*712T>G (n.*712T>G)
c.634T>G (p.Leu212Val)
c.*836T>G (n.*836T>G)
c.874T>G (p.Leu292Val)
c.*701T>G (n.*701T>G)
8g.43122741T>ACA371122959POMKc.917T>A (p.Leu306Ter)
c.*713T>A (n.*713T>A)
c.635T>A (p.Leu212Ter)
c.*837T>A (n.*837T>A)
c.875T>A (p.Leu292Ter)
c.*702T>A (n.*702T>A)
8g.43122741T>CCA371122958POMKc.917T>C (p.Leu306Ser)
c.*713T>C (n.*713T>C)
c.635T>C (p.Leu212Ser)
c.*837T>C (n.*837T>C)
c.875T>C (p.Leu292Ser)
c.*702T>C (n.*702T>C)
8g.43122741T>GCA371122957POMKc.917T>G (p.Leu306Trp)
c.*713T>G (n.*713T>G)
c.635T>G (p.Leu212Trp)
c.*837T>G (n.*837T>G)
c.875T>G (p.Leu292Trp)
c.*702T>G (n.*702T>G)
8g.43122742G>ACA460787447POMKc.918G>A (p.Leu306=)
c.*714G>A (n.*714G>A)
c.636G>A (p.Leu212=)
c.*838G>A (n.*838G>A)
c.876G>A (p.Leu292=)
c.*703G>A (n.*703G>A)
8g.43122742G>CCA371122960POMKc.918G>C (p.Leu306Phe)
c.*714G>C (n.*714G>C)
c.636G>C (p.Leu212Phe)
c.*838G>C (n.*838G>C)
c.876G>C (p.Leu292Phe)
c.*703G>C (n.*703G>C)
8g.43122742G>TCA371122961POMKc.918G>T (p.Leu306Phe)
c.*714G>T (n.*714G>T)
c.636G>T (p.Leu212Phe)
c.*838G>T (n.*838G>T)
c.876G>T (p.Leu292Phe)
c.*703G>T (n.*703G>T)
8g.43122743T>ACA371122962POMKc.919T>A (p.Phe307Ile)
c.*715T>A (n.*715T>A)
c.637T>A (p.Phe213Ile)
c.*839T>A (n.*839T>A)
c.877T>A (p.Phe293Ile)
c.*704T>A (n.*704T>A)
8g.43122743T>CCA176080751POMKc.919T>C (p.Phe307Leu)
c.*715T>C (n.*715T>C)
c.637T>C (p.Phe213Leu)
c.*839T>C (n.*839T>C)
c.877T>C (p.Phe293Leu)
c.*704T>C (n.*704T>C)
dbSNP
8g.43122743T>GCA371122963POMKc.919T>G (p.Phe307Val)
c.*715T>G (n.*715T>G)
c.637T>G (p.Phe213Val)
c.*839T>G (n.*839T>G)
c.877T>G (p.Phe293Val)
c.*704T>G (n.*704T>G)
8g.43122743T=CA1779747950POMKc.919T= (p.Phe307=)
c.*715T= (n.*715T=)
c.637T= (p.Phe213=)
c.*839T= (n.*839T=)
c.877T= (p.Phe293=)
c.*704T= (n.*704T=)
8g.43122744T>ACA371122964POMKc.920T>A (p.Phe307Tyr)
c.*716T>A (n.*716T>A)
c.638T>A (p.Phe213Tyr)
c.*840T>A (n.*840T>A)
c.878T>A (p.Phe293Tyr)
c.*705T>A (n.*705T>A)
8g.43122744T>CCA371122965POMKc.920T>C (p.Phe307Ser)
c.*716T>C (n.*716T>C)
c.638T>C (p.Phe213Ser)
c.*840T>C (n.*840T>C)
c.878T>C (p.Phe293Ser)
c.*705T>C (n.*705T>C)
gnomAD v4
8g.43122744T>GCA371122966POMKc.920T>G (p.Phe307Cys)
c.*716T>G (n.*716T>G)
c.638T>G (p.Phe213Cys)
c.*840T>G (n.*840T>G)
c.878T>G (p.Phe293Cys)
c.*705T>G (n.*705T>G)
8g.43122745T>ACA371122967POMKc.921T>A (p.Phe307Leu)
c.*717T>A (n.*717T>A)
c.639T>A (p.Phe213Leu)
c.*841T>A (n.*841T>A)
c.879T>A (p.Phe293Leu)
c.*706T>A (n.*706T>A)
8g.43122745T>CCA460787449POMKc.921T>C (p.Phe307=)
c.*717T>C (n.*717T>C)
c.639T>C (p.Phe213=)
c.*841T>C (n.*841T>C)
c.879T>C (p.Phe293=)
c.*706T>C (n.*706T>C)
8g.43122745T>GCA371122968POMKc.921T>G (p.Phe307Leu)
c.*717T>G (n.*717T>G)
c.639T>G (p.Phe213Leu)
c.*841T>G (n.*841T>G)
c.879T>G (p.Phe293Leu)
c.*706T>G (n.*706T>G)
8g.43122746G>ACA371122969POMKc.922G>A (p.Asp308Asn)
c.*718G>A (n.*718G>A)
c.640G>A (p.Asp214Asn)
c.*842G>A (n.*842G>A)
c.880G>A (p.Asp294Asn)
c.*707G>A (n.*707G>A)
8g.43122746G>CCA371122970POMKc.922G>C (p.Asp308His)
c.*718G>C (n.*718G>C)
c.640G>C (p.Asp214His)
c.*842G>C (n.*842G>C)
c.880G>C (p.Asp294His)
c.*707G>C (n.*707G>C)
8g.43122746G>TCA371122971POMKc.922G>T (p.Asp308Tyr)
c.*718G>T (n.*718G>T)
c.640G>T (p.Asp214Tyr)
c.*842G>T (n.*842G>T)
c.880G>T (p.Asp294Tyr)
c.*707G>T (n.*707G>T)
gnomAD v4
8g.43122747A>CCA371122973POMKc.923A>C (p.Asp308Ala)
c.*719A>C (n.*719A>C)
c.641A>C (p.Asp214Ala)
c.*843A>C (n.*843A>C)
c.881A>C (p.Asp294Ala)
c.*708A>C (n.*708A>C)
8g.43122747A>GCA371122974POMKc.923A>G (p.Asp308Gly)
c.*719A>G (n.*719A>G)
c.641A>G (p.Asp214Gly)
c.*843A>G (n.*843A>G)
c.881A>G (p.Asp294Gly)
c.*708A>G (n.*708A>G)
gnomAD v4
8g.43122747A>TCA371122972POMKc.923A>T (p.Asp308Val)
c.*719A>T (n.*719A>T)
c.641A>T (p.Asp214Val)
c.*843A>T (n.*843A>T)
c.881A>T (p.Asp294Val)
c.*708A>T (n.*708A>T)
8g.43122748T>ACA371122975POMKc.924T>A (p.Asp308Glu)
c.*720T>A (n.*720T>A)
c.642T>A (p.Asp214Glu)
c.*844T>A (n.*844T>A)
c.882T>A (p.Asp294Glu)
c.*709T>A (n.*709T>A)
8g.43122748T>CCA460787517POMKc.924T>C (p.Asp308=)
c.*720T>C (n.*720T>C)
c.642T>C (p.Asp214=)
c.*844T>C (n.*844T>C)
c.882T>C (p.Asp294=)
c.*709T>C (n.*709T>C)
8g.43122748T>GCA371122976POMKc.924T>G (p.Asp308Glu)
c.*720T>G (n.*720T>G)
c.642T>G (p.Asp214Glu)
c.*844T>G (n.*844T>G)
c.882T>G (p.Asp294Glu)
c.*709T>G (n.*709T>G)
8g.43122749A>CCA371122977POMKc.925A>C (p.Ile309Leu)
c.*721A>C (n.*721A>C)
c.643A>C (p.Ile215Leu)
c.*845A>C (n.*845A>C)
c.883A>C (p.Ile295Leu)
c.*710A>C (n.*710A>C)
8g.43122749A>GCA371122978POMKc.925A>G (p.Ile309Val)
c.*721A>G (n.*721A>G)
c.643A>G (p.Ile215Val)
c.*845A>G (n.*845A>G)
c.883A>G (p.Ile295Val)
c.*710A>G (n.*710A>G)
8g.43122749A>TCA371122979POMKc.925A>T (p.Ile309Phe)
c.*721A>T (n.*721A>T)
c.643A>T (p.Ile215Phe)
c.*845A>T (n.*845A>T)
c.883A>T (p.Ile295Phe)
c.*710A>T (n.*710A>T)
8g.43122750T>ACA371122980POMKc.926T>A (p.Ile309Asn)
c.*722T>A (n.*722T>A)
c.644T>A (p.Ile215Asn)
c.*846T>A (n.*846T>A)
c.884T>A (p.Ile295Asn)
c.*711T>A (n.*711T>A)
gnomAD v4
8g.43122750T>CCA4736379POMKc.926T>C (p.Ile309Thr)
c.*722T>C (n.*722T>C)
c.644T>C (p.Ile215Thr)
c.*846T>C (n.*846T>C)
c.884T>C (p.Ile295Thr)
c.*711T>C (n.*711T>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.43122750T>GCA371122981POMKc.926T>G (p.Ile309Ser)
c.*722T>G (n.*722T>G)
c.644T>G (p.Ile215Ser)
c.*846T>G (n.*846T>G)
c.884T>G (p.Ile295Ser)
c.*711T>G (n.*711T>G)
8g.43122750T=CA1779748162POMKc.926T= (p.Ile309=)
c.*722T= (n.*722T=)
c.644T= (p.Ile215=)
c.*846T= (n.*846T=)
c.884T= (p.Ile295=)
c.*711T= (n.*711T=)
8g.43122751T>ACA460787518POMKc.927T>A (p.Ile309=)
c.*723T>A (n.*723T>A)
c.645T>A (p.Ile215=)
c.*847T>A (n.*847T>A)
c.885T>A (p.Ile295=)
c.*712T>A (n.*712T>A)
8g.43122751T>CCA460787519POMKc.927T>C (p.Ile309=)
c.*723T>C (n.*723T>C)
c.645T>C (p.Ile215=)
c.*847T>C (n.*847T>C)
c.885T>C (p.Ile295=)
c.*712T>C (n.*712T>C)
8g.43122751T>GCA371122982POMKc.927T>G (p.Ile309Met)
c.*723T>G (n.*723T>G)
c.645T>G (p.Ile215Met)
c.*847T>G (n.*847T>G)
c.885T>G (p.Ile295Met)
c.*712T>G (n.*712T>G)
8g.43122752C>ACA371122983POMKc.928C>A (p.His310Asn)
c.*724C>A (n.*724C>A)
c.646C>A (p.His216Asn)
c.*848C>A (n.*848C>A)
c.886C>A (p.His296Asn)
c.*713C>A (n.*713C>A)
8g.43122752C>GCA371122984POMKc.928C>G (p.His310Asp)
c.*724C>G (n.*724C>G)
c.646C>G (p.His216Asp)
c.*848C>G (n.*848C>G)
c.886C>G (p.His296Asp)
c.*713C>G (n.*713C>G)
8g.43122752C>TCA371122985POMKc.928C>T (p.His310Tyr)
c.*724C>T (n.*724C>T)
c.646C>T (p.His216Tyr)
c.*848C>T (n.*848C>T)
c.886C>T (p.His296Tyr)
c.*713C>T (n.*713C>T)
8g.43122753A>CCA371122986POMKc.929A>C (p.His310Pro)
c.*725A>C (n.*725A>C)
c.647A>C (p.His216Pro)
c.*849A>C (n.*849A>C)
c.887A>C (p.His296Pro)
c.*714A>C (n.*714A>C)

Number of alleles fetched