Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.72007634C>ACA253729CHST3c.603C>A (p.Tyr201Ter)
ClinVar dbSNP
10g.72007634C=CA1918976010CHST3c.603C= (p.Tyr201=)
10g.72007634C>GCA377145137CHST3c.603C>G (p.Tyr201Ter)
10g.72007634C>TCA470284206CHST3c.603C>T (p.Tyr201=)
dbSNP gnomAD v4
10g.72007635G>ACA377145142CHST3c.604G>A (p.Val202Met)
gnomAD v4 COSMIC
10g.72007635G>CCA377145145CHST3c.604G>C (p.Val202Leu)
dbSNP gnomAD v3 gnomAD v4
10g.72007635G=CA1918976018CHST3c.604G= (p.Val202=)
10g.72007635G>TCA377145147CHST3c.604G>T (p.Val202Leu)
dbSNP gnomAD v4
10g.72007636T>ACA377145151CHST3c.605T>A (p.Val202Glu)
10g.72007636T>CCA377145157CHST3c.605T>C (p.Val202Ala)
dbSNP gnomAD v3 gnomAD v4
10g.72007636T>GCA377145163CHST3c.605T>G (p.Val202Gly)
gnomAD v4
10g.72007636T=CA1918976022CHST3c.605T= (p.Val202=)
10g.72007637G>ACA470284222CHST3c.606G>A (p.Val202=)
gnomAD v4
10g.72007637G>CCA470284224CHST3c.606G>C (p.Val202=)
10g.72007637G>TCA470284227CHST3c.606G>T (p.Val202=)
gnomAD v4
10g.72007638C>ACA377145166CHST3c.607C>A (p.Leu203Met)
10g.72007638C=CA1918976025CHST3c.607C= (p.Leu203=)
10g.72007638C>GCA377145167CHST3c.607C>G (p.Leu203Val)
10g.72007638C>TCA470284229CHST3c.607C>T (p.Leu203=)
dbSNP gnomAD v4
10g.72007639T>ACA377145173CHST3c.608T>A (p.Leu203Gln)
10g.72007639T>CCA377145180CHST3c.608T>C (p.Leu203Pro)
10g.72007639T>GCA377145198CHST3c.608T>G (p.Leu203Arg)
10g.72007640G>ACA470284237CHST3c.609G>A (p.Leu203=)
10g.72007640G>CCA470284238CHST3c.609G>C (p.Leu203=)
10g.72007640G>TCA470284239CHST3c.609G>T (p.Leu203=)
10g.72007641G>ACA377145204CHST3c.610G>A (p.Glu204Lys)
gnomAD v4
10g.72007641G>CCA377145200CHST3c.610G>C (p.Glu204Gln)
10g.72007641G>TCA377145199CHST3c.610G>T (p.Glu204Ter)
gnomAD v4
10g.72007642A>CCA377145208CHST3c.611A>C (p.Glu204Ala)
10g.72007642A>GCA377145211CHST3c.611A>G (p.Glu204Gly)
10g.72007642A>TCA377145209CHST3c.611A>T (p.Glu204Val)
10g.72007643G>ACA470284245CHST3c.612G>A (p.Glu204=)
gnomAD v4
10g.72007643G>CCA377145215CHST3c.612G>C (p.Glu204Asp)
10g.72007643G>TCA377145216CHST3c.612G>T (p.Glu204Asp)
gnomAD v4
10g.72007644C>ACA377145217CHST3c.613C>A (p.His205Asn)
10g.72007644C>GCA377145219CHST3c.613C>G (p.His205Asp)
10g.72007644C>TCA377145222CHST3c.613C>T (p.His205Tyr)
ClinVar
10g.72007645A>CCA377145225CHST3c.614A>C (p.His205Pro)
10g.72007645A>GCA377145230CHST3c.614A>G (p.His205Arg)
10g.72007645A>TCA377145231CHST3c.614A>T (p.His205Leu)
10g.72007646C>ACA377145232CHST3c.615C>A (p.His205Gln)
10g.72007646C=CA1918976029CHST3c.615C= (p.His205=)
10g.72007646C>GCA377145233CHST3c.615C>G (p.His205Gln)
dbSNP gnomAD v2 gnomAD v4
10g.72007646C>TCA470284263CHST3c.615C>T (p.His205=)
gnomAD v4
10g.72007647T>ACA377145248CHST3c.616T>A (p.Phe206Ile)
10g.72007647T>CCA377145246CHST3c.616T>C (p.Phe206Leu)
10g.72007647T>GCA377145237CHST3c.616T>G (p.Phe206Val)
10g.72007647_72007655delCA2788492303CHST3c.616_624del (p.Phe206_Thr208del)
10g.72007648T>ACA377145254CHST3c.617T>A (p.Phe206Tyr)
10g.72007648T>CCA377145255CHST3c.617T>C (p.Phe206Ser)

Number of alleles fetched