Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.47449438G>ACA229251ZNF41c.332C>T (p.Pro111Leu)
c.362C>T (p.Pro121Leu)
n.485C>T
c.74C>T (p.Pro25Leu)
c.434C>T (p.Pro145Leu)
c.338C>T (p.Pro113Leu)
c.458C>T (p.Pro153Leu)
c.302-72C>T (n.302-72C>T)
c.296-72C>T (n.296-72C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
Xg.47449438G>CCA413058460ZNF41c.332C>G (p.Pro111Arg)
c.362C>G (p.Pro121Arg)
n.485C>G
c.74C>G (p.Pro25Arg)
c.434C>G (p.Pro145Arg)
c.338C>G (p.Pro113Arg)
c.458C>G (p.Pro153Arg)
c.302-72C>G (n.302-72C>G)
c.296-72C>G (n.296-72C>G)
Xg.47449438G=CA2427930901ZNF41c.332C= (p.Pro111=)
c.362C= (p.Pro121=)
n.485C=
c.74C= (p.Pro25=)
c.434C= (p.Pro145=)
c.338C= (p.Pro113=)
c.458C= (p.Pro153=)
c.302-72C= (n.302-72C=)
c.296-72C= (n.296-72C=)
Xg.47449438G>TCA413058461ZNF41c.332C>A (p.Pro111His)
c.362C>A (p.Pro121His)
n.485C>A
c.74C>A (p.Pro25His)
c.434C>A (p.Pro145His)
c.338C>A (p.Pro113His)
c.458C>A (p.Pro153His)
c.302-72C>A (n.302-72C>A)
c.296-72C>A (n.296-72C>A)
Xg.47449439G>ACA413058462ZNF41c.331C>T (p.Pro111Ser)
c.361C>T (p.Pro121Ser)
n.484C>T
c.73C>T (p.Pro25Ser)
c.433C>T (p.Pro145Ser)
c.337C>T (p.Pro113Ser)
c.457C>T (p.Pro153Ser)
c.302-73C>T (n.302-73C>T)
c.296-73C>T (n.296-73C>T)
dbSNP
Xg.47449439G>CCA413058463ZNF41c.331C>G (p.Pro111Ala)
c.361C>G (p.Pro121Ala)
n.484C>G
c.73C>G (p.Pro25Ala)
c.433C>G (p.Pro145Ala)
c.337C>G (p.Pro113Ala)
c.457C>G (p.Pro153Ala)
c.302-73C>G (n.302-73C>G)
c.296-73C>G (n.296-73C>G)
Xg.47449439G>TCA413058464ZNF41c.331C>A (p.Pro111Thr)
c.361C>A (p.Pro121Thr)
n.484C>A
c.73C>A (p.Pro25Thr)
c.433C>A (p.Pro145Thr)
c.337C>A (p.Pro113Thr)
c.457C>A (p.Pro153Thr)
c.302-73C>A (n.302-73C>A)
c.296-73C>A (n.296-73C>A)
COSMIC COSMIC
Xg.47449440A>CCA413058465ZNF41c.330T>G (p.Ile110Met)
c.360T>G (p.Ile120Met)
n.483T>G
c.72T>G (p.Ile24Met)
c.432T>G (p.Ile144Met)
c.336T>G (p.Ile112Met)
c.456T>G (p.Ile152Met)
c.302-74T>G (n.302-74T>G)
c.296-74T>G (n.296-74T>G)
Xg.47449440A>GCA516373112ZNF41c.330T>C (p.Ile110=)
c.360T>C (p.Ile120=)
n.483T>C
c.72T>C (p.Ile24=)
c.432T>C (p.Ile144=)
c.336T>C (p.Ile112=)
c.456T>C (p.Ile152=)
c.302-74T>C (n.302-74T>C)
c.296-74T>C (n.296-74T>C)
Xg.47449440A>TCA516373114ZNF41c.330T>A (p.Ile110=)
c.360T>A (p.Ile120=)
n.483T>A
c.72T>A (p.Ile24=)
c.432T>A (p.Ile144=)
c.336T>A (p.Ile112=)
c.456T>A (p.Ile152=)
c.302-74T>A (n.302-74T>A)
c.296-74T>A (n.296-74T>A)
Xg.47449441A>CCA413058466ZNF41c.329T>G (p.Ile110Ser)
c.359T>G (p.Ile120Ser)
n.482T>G
c.71T>G (p.Ile24Ser)
c.431T>G (p.Ile144Ser)
c.335T>G (p.Ile112Ser)
c.455T>G (p.Ile152Ser)
c.302-75T>G (n.302-75T>G)
c.296-75T>G (n.296-75T>G)
Xg.47449441A>GCA413058467ZNF41c.329T>C (p.Ile110Thr)
c.359T>C (p.Ile120Thr)
n.482T>C
c.71T>C (p.Ile24Thr)
c.431T>C (p.Ile144Thr)
c.335T>C (p.Ile112Thr)
c.455T>C (p.Ile152Thr)
c.302-75T>C (n.302-75T>C)
c.296-75T>C (n.296-75T>C)
Xg.47449441A>TCA413058468ZNF41c.329T>A (p.Ile110Asn)
c.359T>A (p.Ile120Asn)
n.482T>A
c.71T>A (p.Ile24Asn)
c.431T>A (p.Ile144Asn)
c.335T>A (p.Ile112Asn)
c.455T>A (p.Ile152Asn)
c.302-75T>A (n.302-75T>A)
c.296-75T>A (n.296-75T>A)
Xg.47449442T>ACA413058470ZNF41c.328A>T (p.Ile110Phe)
c.358A>T (p.Ile120Phe)
n.481A>T
c.70A>T (p.Ile24Phe)
c.430A>T (p.Ile144Phe)
c.334A>T (p.Ile112Phe)
c.454A>T (p.Ile152Phe)
c.302-76A>T (n.302-76A>T)
c.296-76A>T (n.296-76A>T)
Xg.47449442T>CCA413058471ZNF41c.328A>G (p.Ile110Val)
c.358A>G (p.Ile120Val)
n.481A>G
c.70A>G (p.Ile24Val)
c.430A>G (p.Ile144Val)
c.334A>G (p.Ile112Val)
c.454A>G (p.Ile152Val)
c.302-76A>G (n.302-76A>G)
c.296-76A>G (n.296-76A>G)
Xg.47449442T>GCA413058469ZNF41c.328A>C (p.Ile110Leu)
c.358A>C (p.Ile120Leu)
n.481A>C
c.70A>C (p.Ile24Leu)
c.430A>C (p.Ile144Leu)
c.334A>C (p.Ile112Leu)
c.454A>C (p.Ile152Leu)
c.302-76A>C (n.302-76A>C)
c.296-76A>C (n.296-76A>C)
Xg.47449443T>ACA516373116ZNF41c.327A>T (p.Gly109=)
c.357A>T (p.Gly119=)
n.480A>T
c.69A>T (p.Gly23=)
c.429A>T (p.Gly143=)
c.333A>T (p.Gly111=)
c.453A>T (p.Gly151=)
c.302-77A>T (n.302-77A>T)
c.296-77A>T (n.296-77A>T)
Xg.47449443T>CCA516373118ZNF41c.327A>G (p.Gly109=)
c.357A>G (p.Gly119=)
n.480A>G
c.69A>G (p.Gly23=)
c.429A>G (p.Gly143=)
c.333A>G (p.Gly111=)
c.453A>G (p.Gly151=)
c.302-77A>G (n.302-77A>G)
c.296-77A>G (n.296-77A>G)
Xg.47449443T>GCA516373117ZNF41c.327A>C (p.Gly109=)
c.357A>C (p.Gly119=)
n.480A>C
c.69A>C (p.Gly23=)
c.429A>C (p.Gly143=)
c.333A>C (p.Gly111=)
c.453A>C (p.Gly151=)
c.302-77A>C (n.302-77A>C)
c.296-77A>C (n.296-77A>C)
Xg.47449444C>ACA413058472ZNF41c.326G>T (p.Gly109Val)
c.356G>T (p.Gly119Val)
n.479G>T
c.68G>T (p.Gly23Val)
c.428G>T (p.Gly143Val)
c.332G>T (p.Gly111Val)
c.452G>T (p.Gly151Val)
c.302-78G>T (n.302-78G>T)
c.296-78G>T (n.296-78G>T)
Xg.47449444C=CA2427930902ZNF41c.326G= (p.Gly109=)
c.356G= (p.Gly119=)
n.479G=
c.68G= (p.Gly23=)
c.428G= (p.Gly143=)
c.332G= (p.Gly111=)
c.452G= (p.Gly151=)
c.302-78G= (n.302-78G=)
c.296-78G= (n.296-78G=)
Xg.47449444C>GCA413058473ZNF41c.326G>C (p.Gly109Ala)
c.356G>C (p.Gly119Ala)
n.479G>C
c.68G>C (p.Gly23Ala)
c.428G>C (p.Gly143Ala)
c.332G>C (p.Gly111Ala)
c.452G>C (p.Gly151Ala)
c.302-78G>C (n.302-78G>C)
c.296-78G>C (n.296-78G>C)
Xg.47449444C>TCA413058474ZNF41c.326G>A (p.Gly109Glu)
c.356G>A (p.Gly119Glu)
n.479G>A
c.68G>A (p.Gly23Glu)
c.428G>A (p.Gly143Glu)
c.332G>A (p.Gly111Glu)
c.452G>A (p.Gly151Glu)
c.302-78G>A (n.302-78G>A)
c.296-78G>A (n.296-78G>A)
dbSNP gnomAD v3 gnomAD v4
Xg.47449445C>ACA413058475ZNF41c.325G>T (p.Gly109Ter)
c.355G>T (p.Gly119Ter)
n.478G>T
c.67G>T (p.Gly23Ter)
c.427G>T (p.Gly143Ter)
c.331G>T (p.Gly111Ter)
c.451G>T (p.Gly151Ter)
c.302-79G>T (n.302-79G>T)
c.296-79G>T (n.296-79G>T)
Xg.47449445C>GCA413058476ZNF41c.325G>C (p.Gly109Arg)
c.355G>C (p.Gly119Arg)
n.478G>C
c.67G>C (p.Gly23Arg)
c.427G>C (p.Gly143Arg)
c.331G>C (p.Gly111Arg)
c.451G>C (p.Gly151Arg)
c.302-79G>C (n.302-79G>C)
c.296-79G>C (n.296-79G>C)
Xg.47449445C>TCA413058477ZNF41c.325G>A (p.Gly109Arg)
c.355G>A (p.Gly119Arg)
n.478G>A
c.67G>A (p.Gly23Arg)
c.427G>A (p.Gly143Arg)
c.331G>A (p.Gly111Arg)
c.451G>A (p.Gly151Arg)
c.302-79G>A (n.302-79G>A)
c.296-79G>A (n.296-79G>A)
Xg.47449446C>ACA413058478ZNF41c.324G>T (p.Gln108His)
c.354G>T (p.Gln118His)
n.477G>T
c.66G>T (p.Gln22His)
c.426G>T (p.Gln142His)
c.330G>T (p.Gln110His)
c.450G>T (p.Gln150His)
c.302-80G>T (n.302-80G>T)
c.296-80G>T (n.296-80G>T)
Xg.47449446C>GCA413058479ZNF41c.324G>C (p.Gln108His)
c.354G>C (p.Gln118His)
n.477G>C
c.66G>C (p.Gln22His)
c.426G>C (p.Gln142His)
c.330G>C (p.Gln110His)
c.450G>C (p.Gln150His)
c.302-80G>C (n.302-80G>C)
c.296-80G>C (n.296-80G>C)
Xg.47449446C>TCA516373121ZNF41c.324G>A (p.Gln108=)
c.354G>A (p.Gln118=)
n.477G>A
c.66G>A (p.Gln22=)
c.426G>A (p.Gln142=)
c.330G>A (p.Gln110=)
c.450G>A (p.Gln150=)
c.302-80G>A (n.302-80G>A)
c.296-80G>A (n.296-80G>A)
Xg.47449447T>ACA413058480ZNF41c.323A>T (p.Gln108Leu)
c.353A>T (p.Gln118Leu)
n.476A>T
c.65A>T (p.Gln22Leu)
c.425A>T (p.Gln142Leu)
c.329A>T (p.Gln110Leu)
c.449A>T (p.Gln150Leu)
c.302-81A>T (n.302-81A>T)
c.296-81A>T (n.296-81A>T)
Xg.47449447T>CCA413058481ZNF41c.323A>G (p.Gln108Arg)
c.353A>G (p.Gln118Arg)
n.476A>G
c.65A>G (p.Gln22Arg)
c.425A>G (p.Gln142Arg)
c.329A>G (p.Gln110Arg)
c.449A>G (p.Gln150Arg)
c.302-81A>G (n.302-81A>G)
c.296-81A>G (n.296-81A>G)
Xg.47449447T>GCA413058482ZNF41c.323A>C (p.Gln108Pro)
c.353A>C (p.Gln118Pro)
n.476A>C
c.65A>C (p.Gln22Pro)
c.425A>C (p.Gln142Pro)
c.329A>C (p.Gln110Pro)
c.449A>C (p.Gln150Pro)
c.302-81A>C (n.302-81A>C)
c.296-81A>C (n.296-81A>C)
Xg.47449448G>ACA413058483ZNF41c.322C>T (p.Gln108Ter)
c.352C>T (p.Gln118Ter)
n.475C>T
c.64C>T (p.Gln22Ter)
c.424C>T (p.Gln142Ter)
c.328C>T (p.Gln110Ter)
c.448C>T (p.Gln150Ter)
c.302-82C>T (n.302-82C>T)
c.296-82C>T (n.296-82C>T)
Xg.47449448G>CCA413058484ZNF41c.322C>G (p.Gln108Glu)
c.352C>G (p.Gln118Glu)
n.475C>G
c.64C>G (p.Gln22Glu)
c.424C>G (p.Gln142Glu)
c.328C>G (p.Gln110Glu)
c.448C>G (p.Gln150Glu)
c.302-82C>G (n.302-82C>G)
c.296-82C>G (n.296-82C>G)
Xg.47449448G>TCA413058485ZNF41c.322C>A (p.Gln108Lys)
c.352C>A (p.Gln118Lys)
n.475C>A
c.64C>A (p.Gln22Lys)
c.424C>A (p.Gln142Lys)
c.328C>A (p.Gln110Lys)
c.448C>A (p.Gln150Lys)
c.302-82C>A (n.302-82C>A)
c.296-82C>A (n.296-82C>A)
Xg.47449449T>ACA413058487ZNF41c.321A>T (p.Gln107His)
c.351A>T (p.Gln117His)
n.474A>T
c.63A>T (p.Gln21His)
c.423A>T (p.Gln141His)
c.327A>T (p.Gln109His)
c.447A>T (p.Gln149His)
c.302-83A>T (n.302-83A>T)
c.296-83A>T (n.296-83A>T)
Xg.47449449T>CCA516373123ZNF41c.321A>G (p.Gln107=)
c.351A>G (p.Gln117=)
n.474A>G
c.63A>G (p.Gln21=)
c.423A>G (p.Gln141=)
c.327A>G (p.Gln109=)
c.447A>G (p.Gln149=)
c.302-83A>G (n.302-83A>G)
c.296-83A>G (n.296-83A>G)
dbSNP gnomAD v2 gnomAD v4
Xg.47449449T>GCA413058486ZNF41c.321A>C (p.Gln107His)
c.351A>C (p.Gln117His)
n.474A>C
c.63A>C (p.Gln21His)
c.423A>C (p.Gln141His)
c.327A>C (p.Gln109His)
c.447A>C (p.Gln149His)
c.302-83A>C (n.302-83A>C)
c.296-83A>C (n.296-83A>C)
Xg.47449449T=CA2427930903ZNF41c.321A= (p.Gln107=)
c.351A= (p.Gln117=)
n.474A=
c.63A= (p.Gln21=)
c.423A= (p.Gln141=)
c.327A= (p.Gln109=)
c.447A= (p.Gln149=)
c.302-83A= (n.302-83A=)
c.296-83A= (n.296-83A=)
Xg.47449450T>ACA413058488ZNF41c.320A>T (p.Gln107Leu)
c.350A>T (p.Gln117Leu)
n.473A>T
c.62A>T (p.Gln21Leu)
c.422A>T (p.Gln141Leu)
c.326A>T (p.Gln109Leu)
c.446A>T (p.Gln149Leu)
c.302-84A>T (n.302-84A>T)
c.296-84A>T (n.296-84A>T)
Xg.47449450T>CCA413058489ZNF41c.320A>G (p.Gln107Arg)
c.350A>G (p.Gln117Arg)
n.473A>G
c.62A>G (p.Gln21Arg)
c.422A>G (p.Gln141Arg)
c.326A>G (p.Gln109Arg)
c.446A>G (p.Gln149Arg)
c.302-84A>G (n.302-84A>G)
c.296-84A>G (n.296-84A>G)
Xg.47449450T>GCA413058490ZNF41c.320A>C (p.Gln107Pro)
c.350A>C (p.Gln117Pro)
n.473A>C
c.62A>C (p.Gln21Pro)
c.422A>C (p.Gln141Pro)
c.326A>C (p.Gln109Pro)
c.446A>C (p.Gln149Pro)
c.302-84A>C (n.302-84A>C)
c.296-84A>C (n.296-84A>C)
Xg.47449451G>ACA413058491ZNF41c.319C>T (p.Gln107Ter)
c.349C>T (p.Gln117Ter)
n.472C>T
c.61C>T (p.Gln21Ter)
c.421C>T (p.Gln141Ter)
c.325C>T (p.Gln109Ter)
c.445C>T (p.Gln149Ter)
c.302-85C>T (n.302-85C>T)
c.296-85C>T (n.296-85C>T)
Xg.47449451G>CCA413058492ZNF41c.319C>G (p.Gln107Glu)
c.349C>G (p.Gln117Glu)
n.472C>G
c.61C>G (p.Gln21Glu)
c.421C>G (p.Gln141Glu)
c.325C>G (p.Gln109Glu)
c.445C>G (p.Gln149Glu)
c.302-85C>G (n.302-85C>G)
c.296-85C>G (n.296-85C>G)
Xg.47449451G>TCA413058493ZNF41c.319C>A (p.Gln107Lys)
c.349C>A (p.Gln117Lys)
n.472C>A
c.61C>A (p.Gln21Lys)
c.421C>A (p.Gln141Lys)
c.325C>A (p.Gln109Lys)
c.445C>A (p.Gln149Lys)
c.302-85C>A (n.302-85C>A)
c.296-85C>A (n.296-85C>A)
Xg.47449452C>ACA413058495ZNF41c.318G>T (p.Gln106His)
c.348G>T (p.Gln116His)
n.471G>T
c.60G>T (p.Gln20His)
c.420G>T (p.Gln140His)
c.324G>T (p.Gln108His)
c.444G>T (p.Gln148His)
c.302-86G>T (n.302-86G>T)
c.296-86G>T (n.296-86G>T)
Xg.47449452C=CA2427930904ZNF41c.318G= (p.Gln106=)
c.348G= (p.Gln116=)
n.471G=
c.60G= (p.Gln20=)
c.420G= (p.Gln140=)
c.324G= (p.Gln108=)
c.444G= (p.Gln148=)
c.302-86G= (n.302-86G=)
c.296-86G= (n.296-86G=)
Xg.47449452C>GCA413058494ZNF41c.318G>C (p.Gln106His)
c.348G>C (p.Gln116His)
n.471G>C
c.60G>C (p.Gln20His)
c.420G>C (p.Gln140His)
c.324G>C (p.Gln108His)
c.444G>C (p.Gln148His)
c.302-86G>C (n.302-86G>C)
c.296-86G>C (n.296-86G>C)
Xg.47449452C>TCA329720552ZNF41c.318G>A (p.Gln106=)
c.348G>A (p.Gln116=)
n.471G>A
c.60G>A (p.Gln20=)
c.420G>A (p.Gln140=)
c.324G>A (p.Gln108=)
c.444G>A (p.Gln148=)
c.302-86G>A (n.302-86G>A)
c.296-86G>A (n.296-86G>A)
dbSNP gnomAD v3 gnomAD v4
Xg.47449453T>ACA413058496ZNF41c.317A>T (p.Gln106Leu)
c.347A>T (p.Gln116Leu)
n.470A>T
c.59A>T (p.Gln20Leu)
c.419A>T (p.Gln140Leu)
c.323A>T (p.Gln108Leu)
c.443A>T (p.Gln148Leu)
c.302-87A>T (n.302-87A>T)
c.296-87A>T (n.296-87A>T)

Number of alleles fetched