Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.4110558T>ACA403391400MAP2K2n.840A>T
c.401A>T (p.Tyr134Phe)
c.110A>T (p.Tyr37Phe)
n.598A>T
dbSNP
19g.4110558T>CCA180890MAP2K2n.840A>G
c.401A>G (p.Tyr134Cys)
c.110A>G (p.Tyr37Cys)
n.598A>G
ClinVar dbSNP gnomAD v4 COSMIC COSMIC
19g.4110558T>GCA403391401MAP2K2n.840A>C
c.401A>C (p.Tyr134Ser)
c.110A>C (p.Tyr37Ser)
n.598A>C
dbSNP
19g.4110558T=CA2319230179MAP2K2n.840A=
c.401A= (p.Tyr134=)
c.110A= (p.Tyr37=)
n.598A=
19g.4110559A=CA2319230185MAP2K2n.839T=
c.400T= (p.Tyr134=)
c.109T= (p.Tyr37=)
n.597T=
19g.4110559A>CCA403391404MAP2K2n.839T>G
c.400T>G (p.Tyr134Asp)
c.109T>G (p.Tyr37Asp)
n.597T>G
19g.4110559A>GCA119417MAP2K2n.839T>C
c.400T>C (p.Tyr134His)
c.109T>C (p.Tyr37His)
n.597T>C
ClinVar dbSNP
19g.4110559A>TCA403391406MAP2K2n.839T>A
c.400T>A (p.Tyr134Asn)
c.109T>A (p.Tyr37Asn)
n.597T>A
dbSNP
19g.4110560G>ACA9091008MAP2K2n.838C>T
c.399C>T (p.Phe133=)
c.108C>T (p.Phe36=)
n.596C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.4110560G>CCA403391407MAP2K2n.838C>G
c.399C>G (p.Phe133Leu)
c.108C>G (p.Phe36Leu)
n.596C>G
dbSNP
19g.4110560G=CA2319230190MAP2K2n.838C=
c.399C= (p.Phe133=)
c.108C= (p.Phe36=)
n.596C=
19g.4110560G>TCA403391409MAP2K2n.838C>A
c.399C>A (p.Phe133Leu)
c.108C>A (p.Phe36Leu)
n.596C>A
gnomAD v4
19g.4110561A=CA2319230194MAP2K2n.837T=
c.398T= (p.Phe133=)
c.107T= (p.Phe36=)
n.595T=
19g.4110561A>CCA9091009MAP2K2n.837T>G
c.398T>G (p.Phe133Cys)
c.107T>G (p.Phe36Cys)
n.595T>G
dbSNP ExAC gnomAD v2 gnomAD v4
19g.4110561A>GCA403391413MAP2K2n.837T>C
c.398T>C (p.Phe133Ser)
c.107T>C (p.Phe36Ser)
n.595T>C
dbSNP
19g.4110561A>TCA403391414MAP2K2n.837T>A
c.398T>A (p.Phe133Tyr)
c.107T>A (p.Phe36Tyr)
n.595T>A
dbSNP
19g.4110562A>CCA403391417MAP2K2n.836T>G
c.397T>G (p.Phe133Val)
c.106T>G (p.Phe36Val)
n.594T>G
19g.4110562A>GCA403391419MAP2K2n.836T>C
c.397T>C (p.Phe133Leu)
c.106T>C (p.Phe36Leu)
n.594T>C
19g.4110562A>TCA403391422MAP2K2n.836T>A
c.397T>A (p.Phe133Ile)
c.106T>A (p.Phe36Ile)
n.594T>A
19g.4110563G>ACA504987486MAP2K2n.835C>T
c.396C>T (p.Gly132=)
c.105C>T (p.Gly35=)
n.593C>T
dbSNP
19g.4110563G>CCA504987487MAP2K2n.835C>G
c.396C>G (p.Gly132=)
c.105C>G (p.Gly35=)
n.593C>G
19g.4110563G=CA2319230196MAP2K2n.835C=
c.396C= (p.Gly132=)
c.105C= (p.Gly35=)
n.593C=
19g.4110563G>TCA504987488MAP2K2n.835C>A
c.396C>A (p.Gly132=)
c.105C>A (p.Gly35=)
n.593C>A
19g.4110564C>ACA403391424MAP2K2n.834G>T
c.395G>T (p.Gly132Val)
c.104G>T (p.Gly35Val)
n.592G>T
ClinVar dbSNP
19g.4110564C=CA2319230197MAP2K2n.834G=
c.395G= (p.Gly132=)
c.104G= (p.Gly35=)
n.592G=
19g.4110564C>GCA403391425MAP2K2n.834G>C
c.395G>C (p.Gly132Ala)
c.104G>C (p.Gly35Ala)
n.592G>C
dbSNP
19g.4110564C>TCA250288MAP2K2n.834G>A
c.395G>A (p.Gly132Asp)
c.104G>A (p.Gly35Asp)
n.592G>A
ClinVar dbSNP
19g.4110565C>ACA403391427MAP2K2n.833G>T
c.394G>T (p.Gly132Cys)
c.103G>T (p.Gly35Cys)
n.591G>T
dbSNP
19g.4110565C>GCA403391428MAP2K2n.833G>C
c.394G>C (p.Gly132Arg)
c.103G>C (p.Gly35Arg)
n.591G>C
dbSNP
19g.4110565C>TCA403391430MAP2K2n.833G>A
c.394G>A (p.Gly132Ser)
c.103G>A (p.Gly35Ser)
n.591G>A
dbSNP
19g.4110566C>ACA504987490MAP2K2n.832G>T
c.393G>T (p.Val131=)
c.102G>T (p.Val34=)
n.590G>T
19g.4110566C=CA2319230198MAP2K2n.832G=
c.393G= (p.Val131=)
c.102G= (p.Val34=)
n.590G=
19g.4110566C>GCA504987492MAP2K2n.832G>C
c.393G>C (p.Val131=)
c.102G>C (p.Val34=)
n.590G>C
dbSNP
19g.4110566C>TCA504987493MAP2K2n.832G>A
c.393G>A (p.Val131=)
c.102G>A (p.Val34=)
n.590G>A
dbSNP gnomAD v2 gnomAD v4
19g.4110567A>CCA403391435MAP2K2n.831T>G
c.392T>G (p.Val131Gly)
c.101T>G (p.Val34Gly)
n.589T>G
dbSNP gnomAD v4
19g.4110567A>GCA403391434MAP2K2n.831T>C
c.392T>C (p.Val131Ala)
c.101T>C (p.Val34Ala)
n.589T>C
dbSNP
19g.4110567A>TCA403391432MAP2K2n.831T>A
c.392T>A (p.Val131Glu)
c.101T>A (p.Val34Glu)
n.589T>A
dbSNP
19g.4110568C>ACA403391439MAP2K2n.830G>T
c.391G>T (p.Val131Leu)
c.100G>T (p.Val34Leu)
n.588G>T
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.4110568C=CA2319230201MAP2K2n.830G=
c.391G= (p.Val131=)
c.100G= (p.Val34=)
n.588G=
19g.4110568C>GCA403391437MAP2K2n.830G>C
c.391G>C (p.Val131Leu)
c.100G>C (p.Val34Leu)
n.588G>C
dbSNP
19g.4110568C>TCA137932MAP2K2n.830G>A
c.391G>A (p.Val131Met)
c.100G>A (p.Val34Met)
n.588G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.4110569G>ACA9091010MAP2K2n.829C>T
c.390C>T (p.Ile130=)
c.99C>T (p.Ile33=)
n.587C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
19g.4110569G>CCA403391443MAP2K2n.829C>G
c.390C>G (p.Ile130Met)
c.99C>G (p.Ile33Met)
n.587C>G
19g.4110569G=CA2319230208MAP2K2n.829C=
c.390C= (p.Ile130=)
c.99C= (p.Ile33=)
n.587C=
19g.4110569G>TCA504987494MAP2K2n.829C>A
c.390C>A (p.Ile130=)
c.99C>A (p.Ile33=)
n.587C>A
19g.4110570A>CCA403391445MAP2K2n.828T>G
c.389T>G (p.Ile130Ser)
c.98T>G (p.Ile33Ser)
n.586T>G
19g.4110570A>GCA403391447MAP2K2n.828T>C
c.389T>C (p.Ile130Thr)
c.98T>C (p.Ile33Thr)
n.586T>C
19g.4110570A>TCA403391449MAP2K2n.828T>A
c.389T>A (p.Ile130Asn)
c.98T>A (p.Ile33Asn)
n.586T>A
dbSNP
19g.4110571T>ACA403391451MAP2K2n.827A>T
c.388A>T (p.Ile130Phe)
c.97A>T (p.Ile33Phe)
n.585A>T
19g.4110571T>CCA403391454MAP2K2n.827A>G
c.388A>G (p.Ile130Val)
c.97A>G (p.Ile33Val)
n.585A>G
ClinVar dbSNP gnomAD v3 gnomAD v4

Number of alleles fetched