Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.4860257G>ACA356137863MSX1c.358G>A (p.Val120Met)
gnomAD v4
4g.4860257G>CCA356137866MSX1c.358G>C (p.Val120Leu)
4g.4860257G>TCA356137861MSX1c.358G>T (p.Val120Leu)
gnomAD v4
4g.4860258T>ACA356137870MSX1c.359T>A (p.Val120Glu)
4g.4860258T>CCA356137868MSX1c.359T>C (p.Val120Ala)
gnomAD v4
4g.4860258T>GCA2832949MSX1c.359T>G (p.Val120Gly)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.4860258T=CA1435012217MSX1c.359T= (p.Val120=)
4g.4860259G>ACA438365865MSX1c.360G>A (p.Val120=)
dbSNP gnomAD v2 gnomAD v4
4g.4860259G>CCA438365866MSX1c.360G>C (p.Val120=)
4g.4860259G=CA1435012218MSX1c.360G= (p.Val120=)
4g.4860259G>TCA438365867MSX1c.360G>T (p.Val120=)
gnomAD v4
4g.4860264dupCA549707247MSX1c.365dup (p.Leu123ThrfsTer?)
gnomAD v2 gnomAD v4
4g.4860264delCA2669787885MSX1c.365del (p.Gly122AspfsTer?)
gnomAD v4
4g.4860260G>ACA356137874MSX1c.361G>A (p.Gly121Arg)
gnomAD v4
4g.4860260G>CCA356137875MSX1c.361G>C (p.Gly121Arg)
4g.4860260G=CA1435012219MSX1c.361G= (p.Gly121=)
4g.4860260G>TCA2832950MSX1c.361G>T (p.Gly121Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.4860261G>ACA356137878MSX1c.362G>A (p.Gly121Glu)
4g.4860261G>CCA356137880MSX1c.362G>C (p.Gly121Ala)
4g.4860261G>TCA356137881MSX1c.362G>T (p.Gly121Val)
gnomAD v4
4g.4860261_4860266delCA2669787886MSX1c.362_367del (p.Gly121_Leu123delinsVal)
gnomAD v4
4g.4860262G>ACA438365869MSX1c.363G>A (p.Gly121=)
4g.4860262G>CCA438365870MSX1c.363G>C (p.Gly121=)
gnomAD v4
4g.4860262G>TCA438365871MSX1c.363G>T (p.Gly121=)
gnomAD v4
4g.4860263G>ACA2832951MSX1c.364G>A (p.Gly122Arg)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.4860263G>CCA356137884MSX1c.364G>C (p.Gly122Arg)
4g.4860263G=CA1435012220MSX1c.364G= (p.Gly122=)
4g.4860263G>TCA356137886MSX1c.364G>T (p.Gly122Ter)
gnomAD v4
4g.4860264G>ACA124431MSX1c.365G>A (p.Gly122Glu)
ClinVar dbSNP gnomAD v4
4g.4860264G>CCA356137888MSX1c.365G>C (p.Gly122Ala)
gnomAD v4
4g.4860264G=CA1435012222MSX1c.365G= (p.Gly122=)
4g.4860264G>TCA2832952MSX1c.365G>T (p.Gly122Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.4860264_4860267delinsGACTCA1435012221MSX1c.365_368delinsGACT (p.Gly122=)
4g.4860265A=CA1435012224MSX1c.366A= (p.Gly122=)
4g.4860265A>CCA438365873MSX1c.366A>C (p.Gly122=)
dbSNP gnomAD v3 gnomAD v4
4g.4860265A>GCA438365874MSX1c.366A>G (p.Gly122=)
gnomAD v4
4g.4860265A>TCA438365875MSX1c.366A>T (p.Gly122=)
gnomAD v4
4g.4860265dupCA645527044MSX1c.366dup (p.Leu123ThrfsTer?)
COSMIC
4g.4860265_4860267delCA1435012223MSX1c.366_368del (p.Leu123del)
dbSNP
4g.4860265_4860268delinsACTCCA1435012225MSX1c.366_369delinsACTC (p.Gly122=)
4g.4860266C>ACA356137895MSX1c.367C>A (p.Leu123Ile)
4g.4860266C>GCA356137893MSX1c.367C>G (p.Leu123Val)
4g.4860266C>TCA356137891MSX1c.367C>T (p.Leu123Phe)
gnomAD v4
4g.4860269_4860271delCA1058778182MSX1c.370_372del (p.Leu124del)
dbSNP gnomAD v3 gnomAD v4
4g.4860267T>ACA356137897MSX1c.368T>A (p.Leu123His)
gnomAD v4
4g.4860267T>CCA356137899MSX1c.368T>C (p.Leu123Pro)
gnomAD v4
4g.4860267T>GCA356137901MSX1c.368T>G (p.Leu123Arg)
4g.4860268C>ACA438365879MSX1c.369C>A (p.Leu123=)
4g.4860268C=CA1435012226MSX1c.369C= (p.Leu123=)
4g.4860268C>GCA438365880MSX1c.369C>G (p.Leu123=)
gnomAD v4

Number of alleles fetched