Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.133256264G>ACA040427ABOc.467C>T (p.Pro156Leu)
n.478C>T
c.464C>T (p.Pro155Leu)
dbSNP ExAC gnomAD COSMIC
9g.133256264G>CCA375686297ABOc.467C>G (p.Pro156Arg)
n.478C>G
c.464C>G (p.Pro155Arg)
9g.133256264G>TCA375686298ABOc.467C>A (p.Pro156Gln)
n.478C>A
c.464C>A (p.Pro155Gln)
9g.133256265G>ACA375686301ABOc.466C>T (p.Pro156Ser)
n.477C>T
c.463C>T (p.Pro155Ser)
9g.133256265G>CCA375686299ABOc.466C>G (p.Pro156Ala)
n.477C>G
c.463C>G (p.Pro155Ala)
9g.133256265G>TCA375686300ABOc.466C>A (p.Pro156Thr)
n.477C>A
c.463C>A (p.Pro155Thr)
9g.133256266C>ACA375686302ABOc.465G>T (p.Gln155His)
n.476G>T
c.462G>T (p.Gln154His)
9g.133256266C>GCA375686303ABOc.465G>C (p.Gln155His)
n.476G>C
c.462G>C (p.Gln154His)
9g.133256266C>TCA200765562ABOc.465G>A (p.Gln155=)
n.476G>A
c.462G>A (p.Gln154=)
dbSNP
9g.133256267T>ACA375686304ABOc.464A>T (p.Gln155Leu)
n.475A>T
c.461A>T (p.Gln154Leu)
9g.133256267T>CCA375686305ABOc.464A>G (p.Gln155Arg)
n.475A>G
c.461A>G (p.Gln154Arg)
9g.133256267T>GCA375686306ABOc.464A>C (p.Gln155Pro)
n.475A>C
c.461A>C (p.Gln154Pro)
9g.133256268G>ACA5305841ABOc.463C>T (p.Gln155Ter)
n.474C>T
c.460C>T (p.Gln154Ter)
dbSNP ExAC gnomAD
9g.133256268G>CCA375686308ABOc.463C>G (p.Gln155Glu)
n.474C>G
c.460C>G (p.Gln154Glu)
gnomAD
9g.133256268G>TCA375686307ABOc.463C>A (p.Gln155Lys)
n.474C>A
c.460C>A (p.Gln154Lys)
9g.133256269G>ACA5305842ABOc.462C>T (p.Asp154=)
n.473C>T
c.459C>T (p.Asp153=)
dbSNP ExAC gnomAD
9g.133256269G>CCA375686309ABOc.462C>G (p.Asp154Glu)
n.473C>G
c.459C>G (p.Asp153Glu)
9g.133256269G>TCA375686310ABOc.462C>A (p.Asp154Glu)
n.473C>A
c.459C>A (p.Asp153Glu)
9g.133256270T>ACA375686311ABOc.461A>T (p.Asp154Val)
n.472A>T
c.458A>T (p.Asp153Val)
9g.133256270T>CCA375686312ABOc.461A>G (p.Asp154Gly)
n.472A>G
c.458A>G (p.Asp153Gly)
9g.133256270T>GCA375686313ABOc.461A>C (p.Asp154Ala)
n.472A>C
c.458A>C (p.Asp153Ala)
9g.133256271C>ACA375686314ABOc.460G>T (p.Asp154Tyr)
n.471G>T
c.457G>T (p.Asp153Tyr)
9g.133256271C>GCA375686315ABOc.460G>C (p.Asp154His)
n.471G>C
c.457G>C (p.Asp153His)
9g.133256271C>TCA200765570ABOc.460G>A (p.Asp154Asn)
n.471G>A
c.457G>A (p.Asp153Asn)
dbSNP gnomAD COSMIC
9g.133256272G>ACA200765573ABOc.459C>T (p.Thr153=)
n.470C>T
c.456C>T (p.Thr152=)
dbSNP
9g.133256272G>CCA467782935ABOc.459C>G (p.Thr153=)
n.470C>G
c.456C>G (p.Thr152=)
9g.133256272G>TCA467782937ABOc.459C>A (p.Thr153=)
n.470C>A
c.456C>A (p.Thr152=)
9g.133256273G>ACA375686316ABOc.458C>T (p.Thr153Ile)
n.469C>T
c.455C>T (p.Thr152Ile)
9g.133256273G>CCA375686317ABOc.458C>G (p.Thr153Ser)
n.469C>G
c.455C>G (p.Thr152Ser)
gnomAD
9g.133256273G>TCA375686318ABOc.458C>A (p.Thr153Asn)
n.469C>A
c.455C>A (p.Thr152Asn)
9g.133256274T>ACA375686319ABOc.457A>T (p.Thr153Ser)
n.468A>T
c.454A>T (p.Thr152Ser)
9g.133256274T>CCA375686321ABOc.457A>G (p.Thr153Ala)
n.468A>G
c.454A>G (p.Thr152Ala)
9g.133256274T>GCA375686320ABOc.457A>C (p.Thr153Pro)
n.468A>C
c.454A>C (p.Thr152Pro)
9g.133256275G>ACA467782939ABOc.456C>T (p.Phe152=)
n.467C>T
c.453C>T (p.Phe151=)
9g.133256275G>CCA375686322ABOc.456C>G (p.Phe152Leu)
n.467C>G
c.453C>G (p.Phe151Leu)
9g.133256275G>TCA375686323ABOc.456C>A (p.Phe152Leu)
n.467C>A
c.453C>A (p.Phe151Leu)
9g.133256276A>CCA375686324ABOc.455T>G (p.Phe152Cys)
n.466T>G
c.452T>G (p.Phe151Cys)
9g.133256276A>GCA375686325ABOc.455T>C (p.Phe152Ser)
n.466T>C
c.452T>C (p.Phe151Ser)
9g.133256276A>TCA375686326ABOc.455T>A (p.Phe152Tyr)
n.466T>A
c.452T>A (p.Phe151Tyr)
9g.133256277A>CCA375686327ABOc.454T>G (p.Phe152Val)
n.465T>G
c.451T>G (p.Phe151Val)
9g.133256277A>GCA200765576ABOc.454T>C (p.Phe152Leu)
n.465T>C
c.451T>C (p.Phe151Leu)
dbSNP gnomAD
9g.133256277A>TCA375686328ABOc.454T>A (p.Phe152Ile)
n.465T>A
c.451T>A (p.Phe151Ile)
9g.133256278G>ACA467782944ABOc.453C>T (p.Val151=)
n.464C>T
c.450C>T (p.Val150=)
9g.133256278G>CCA467782946ABOc.453C>G (p.Val151=)
n.464C>G
c.450C>G (p.Val150=)
9g.133256278G>TCA467782945ABOc.453C>A (p.Val151=)
n.464C>A
c.450C>A (p.Val150=)
9g.133256279A>CCA375686329ABOc.452T>G (p.Val151Gly)
n.463T>G
c.449T>G (p.Val150Gly)
9g.133256279A>GCA375686330ABOc.452T>C (p.Val151Ala)
n.463T>C
c.449T>C (p.Val150Ala)
9g.133256279A>TCA375686331ABOc.452T>A (p.Val151Asp)
n.463T>A
c.449T>A (p.Val150Asp)
9g.133256280C>ACA375686332ABOc.451G>T (p.Val151Phe)
n.462G>T
c.448G>T (p.Val150Phe)
9g.133256280C>GCA375686333ABOc.451G>C (p.Val151Leu)
n.462G>C
c.448G>C (p.Val150Leu)

Number of alleles fetched