Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.4862779_4862850delCA2760244033MSX1c.548_619del (p.Gln183_Ser207delinsArg)
n.260_331del
4g.4862833_4862834dupCA549707243MSX1c.602_603dup (p.Arg202SerfsTer16)
n.314_315dup
dbSNP gnomAD v2
4g.4862833A>CCA356138454MSX1c.602A>C (p.Glu201Ala)
n.314A>C
4g.4862833A>GCA356138455MSX1c.602A>G (p.Glu201Gly)
n.314A>G
4g.4862833A>TCA356138456MSX1c.602A>T (p.Glu201Val)
n.314A>T
4g.4862834G>ACA438366065MSX1c.603G>A (p.Glu201=)
n.315G>A
4g.4862834G>CCA356138457MSX1c.603G>C (p.Glu201Asp)
n.315G>C
4g.4862834G>TCA356138458MSX1c.603G>T (p.Glu201Asp)
n.315G>T
4g.4862839_4862840delCA2586973674MSX1c.608_609del (p.Ala203GlyfsTer10)
n.320_321del
4g.4862835C>ACA356138460MSX1c.604C>A (p.Arg202Ser)
n.316C>A
4g.4862835C=CA1435013670MSX1c.604C= (p.Arg202=)
n.316C=
4g.4862835C>GCA2833081MSX1c.604C>G (p.Arg202Gly)
n.316C>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.4862835C>TCA356138459MSX1c.604C>T (p.Arg202Cys)
n.316C>T
gnomAD v4
4g.4862836G>ACA356138461MSX1c.605G>A (p.Arg202His)
n.317G>A
ClinVar dbSNP
4g.4862836G>CCA124423MSX1c.605G>C (p.Arg202Pro)
n.317G>C
ClinVar dbSNP
4g.4862836G=CA1435013671MSX1c.605G= (p.Arg202=)
n.317G=
4g.4862836G>TCA356138462MSX1c.605G>T (p.Arg202Leu)
n.317G>T
4g.4862837C>ACA438366069MSX1c.606C>A (p.Arg202=)
n.318C>A
gnomAD v4
4g.4862837C>GCA438366070MSX1c.606C>G (p.Arg202=)
n.318C>G
4g.4862837C>TCA438366071MSX1c.606C>T (p.Arg202=)
n.318C>T
gnomAD v4
4g.4862838G>ACA356138463MSX1c.607G>A (p.Ala203Thr)
n.319G>A
4g.4862838G>CCA356138464MSX1c.607G>C (p.Ala203Pro)
n.319G>C
4g.4862838G=CA1435013672MSX1c.607G= (p.Ala203=)
n.319G=
4g.4862838G>TCA2833082MSX1c.607G>T (p.Ala203Ser)
n.319G>T
dbSNP ExAC gnomAD v2 gnomAD v4
4g.4862839C>ACA356138465MSX1c.608C>A (p.Ala203Glu)
n.320C>A
4g.4862839C=CA1435013673MSX1c.608C= (p.Ala203=)
n.320C=
4g.4862839C>GCA356138466MSX1c.608C>G (p.Ala203Gly)
n.320C>G
dbSNP
4g.4862839C>TCA356138467MSX1c.608C>T (p.Ala203Val)
n.320C>T
dbSNP gnomAD v3 gnomAD v4
4g.4862840G>ACA438366156MSX1c.609G>A (p.Ala203=)
n.321G>A
4g.4862840G>CCA438366157MSX1c.609G>C (p.Ala203=)
n.321G>C
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.4862840G=CA1435013674MSX1c.609G= (p.Ala203=)
n.321G=
4g.4862840G>TCA438366158MSX1c.609G>T (p.Ala203=)
n.321G>T
dbSNP gnomAD v2
4g.4862841G>ACA356138468MSX1c.610G>A (p.Glu204Lys)
n.322G>A
gnomAD v4
4g.4862841G>CCA356138469MSX1c.610G>C (p.Glu204Gln)
n.322G>C
4g.4862841G>TCA356138470MSX1c.610G>T (p.Glu204Ter)
n.322G>T
4g.4862842A>CCA356138473MSX1c.611A>C (p.Glu204Ala)
n.323A>C
4g.4862842A>GCA356138472MSX1c.611A>G (p.Glu204Gly)
n.323A>G
4g.4862842A>TCA356138471MSX1c.611A>T (p.Glu204Val)
n.323A>T
4g.4862843G>ACA438366159MSX1c.612G>A (p.Glu204=)
n.324G>A
4g.4862843G>CCA356138475MSX1c.612G>C (p.Glu204Asp)
n.324G>C
dbSNP gnomAD v4
4g.4862843G=CA1435013675MSX1c.612G= (p.Glu204=)
n.324G=
4g.4862843G>TCA356138474MSX1c.612G>T (p.Glu204Asp)
n.324G>T
4g.4862844T>ACA356138476MSX1c.613T>A (p.Phe205Ile)
n.325T>A
4g.4862844T>CCA2833083MSX1c.613T>C (p.Phe205Leu)
n.325T>C
dbSNP ExAC gnomAD v2 gnomAD v4
4g.4862844T>GCA356138477MSX1c.613T>G (p.Phe205Val)
n.325T>G
4g.4862844T=CA1435013676MSX1c.613T= (p.Phe205=)
n.325T=
4g.4862845T>ACA356138478MSX1c.614T>A (p.Phe205Tyr)
n.326T>A
4g.4862845T>CCA356138479MSX1c.614T>C (p.Phe205Ser)
n.326T>C
gnomAD v4
4g.4862845T>GCA356138480MSX1c.614T>G (p.Phe205Cys)
n.326T>G
4g.4862846C>ACA356138481MSX1c.615C>A (p.Phe205Leu)
n.327C>A

Number of alleles fetched