Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.18400581C>ACA370636195NAT2c.578C>A (p.Thr193Lys)
c.188C>A (p.Thr63Lys)
8g.18400581C=CA1768219048NAT2c.578C= (p.Thr193=)
c.188C= (p.Thr63=)
8g.18400581C>GCA370636196NAT2c.578C>G (p.Thr193Arg)
c.188C>G (p.Thr63Arg)
gnomAD v4
8g.18400581C>TCA4651645NAT2c.578C>T (p.Thr193Met)
c.188C>T (p.Thr63Met)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
8g.18400582G>ACA4651647NAT2c.579G>A (p.Thr193=)
c.189G>A (p.Thr63=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.18400582G>CCA459881268NAT2c.579G>C (p.Thr193=)
c.189G>C (p.Thr63=)
8g.18400582G=CA1768219049NAT2c.579G= (p.Thr193=)
c.189G= (p.Thr63=)
8g.18400582G>TCA4651646NAT2c.579G>T (p.Thr193=)
c.189G>T (p.Thr63=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.18400583C>ACA370636197NAT2c.580C>A (p.Leu194Ile)
c.190C>A (p.Leu64Ile)
8g.18400583C=CA1768219050NAT2c.580C= (p.Leu194=)
c.190C= (p.Leu64=)
8g.18400583C>GCA4651648NAT2c.580C>G (p.Leu194Val)
c.190C>G (p.Leu64Val)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.18400583C>TCA370636198NAT2c.580C>T (p.Leu194Phe)
c.190C>T (p.Leu64Phe)
gnomAD v4
8g.18400584T>ACA370636199NAT2c.581T>A (p.Leu194His)
c.191T>A (p.Leu64His)
8g.18400584T>CCA370636200NAT2c.581T>C (p.Leu194Pro)
c.191T>C (p.Leu64Pro)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.18400584T>GCA370636201NAT2c.581T>G (p.Leu194Arg)
c.191T>G (p.Leu64Arg)
8g.18400584T=CA1768219051NAT2c.581T= (p.Leu194=)
c.191T= (p.Leu64=)
8g.18400585T>ACA459881270NAT2c.582T>A (p.Leu194=)
c.192T>A (p.Leu64=)
8g.18400585T>CCA459881271NAT2c.582T>C (p.Leu194=)
c.192T>C (p.Leu64=)
8g.18400585T>GCA459881269NAT2c.582T>G (p.Leu194=)
c.192T>G (p.Leu64=)
8g.18400586G>ACA370636203NAT2c.583G>A (p.Glu195Lys)
c.193G>A (p.Glu65Lys)
8g.18400586G>CCA4651649NAT2c.583G>C (p.Glu195Gln)
c.193G>C (p.Glu65Gln)
dbSNP ExAC gnomAD v2 gnomAD v4
8g.18400586G=CA1768219052NAT2c.583G= (p.Glu195=)
c.193G= (p.Glu65=)
8g.18400586G>TCA370636202NAT2c.583G>T (p.Glu195Ter)
c.193G>T (p.Glu65Ter)
gnomAD v3 gnomAD v4
8g.18400587A>CCA370636204NAT2c.584A>C (p.Glu195Ala)
c.194A>C (p.Glu65Ala)
gnomAD v4
8g.18400587A>GCA370636205NAT2c.584A>G (p.Glu195Gly)
c.194A>G (p.Glu65Gly)
8g.18400587A>TCA370636206NAT2c.584A>T (p.Glu195Val)
c.194A>T (p.Glu65Val)
8g.18400588A>CCA370636207NAT2c.585A>C (p.Glu195Asp)
c.195A>C (p.Glu65Asp)
8g.18400588A>GCA459881272NAT2c.585A>G (p.Glu195=)
c.195A>G (p.Glu65=)
8g.18400588A>TCA370636208NAT2c.585A>T (p.Glu195Asp)
c.195A>T (p.Glu65Asp)
8g.18400589C>ACA4651650NAT2c.586C>A (p.Pro196Thr)
c.196C>A (p.Pro66Thr)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.18400589C=CA1768219053NAT2c.586C= (p.Pro196=)
c.196C= (p.Pro66=)
8g.18400589C>GCA370636210NAT2c.586C>G (p.Pro196Ala)
c.196C>G (p.Pro66Ala)
dbSNP gnomAD v4
8g.18400589C>TCA370636209NAT2c.586C>T (p.Pro196Ser)
c.196C>T (p.Pro66Ser)
gnomAD v4
8g.18400590C>ACA370636211NAT2c.587C>A (p.Pro196His)
c.197C>A (p.Pro66His)
8g.18400590C=CA1768219054NAT2c.587C= (p.Pro196=)
c.197C= (p.Pro66=)
8g.18400590C>GCA4651651NAT2c.587C>G (p.Pro196Arg)
c.197C>G (p.Pro66Arg)
dbSNP ExAC gnomAD v2 gnomAD v4
8g.18400590C>TCA370636212NAT2c.587C>T (p.Pro196Leu)
c.197C>T (p.Pro66Leu)
8g.18400591T>ACA459881273NAT2c.588T>A (p.Pro196=)
c.198T>A (p.Pro66=)
8g.18400591T>CCA459881274NAT2c.588T>C (p.Pro196=)
c.198T>C (p.Pro66=)
8g.18400591T>GCA459881275NAT2c.588T>G (p.Pro196=)
c.198T>G (p.Pro66=)
gnomAD v4
8g.18400592C>ACA173519931NAT2c.589C>A (p.Arg197=)
c.199C>A (p.Arg67=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.18400592C=CA1768219055NAT2c.589C= (p.Arg197=)
c.199C= (p.Arg67=)
8g.18400592C>GCA370636213NAT2c.589C>G (p.Arg197Gly)
c.199C>G (p.Arg67Gly)
8g.18400592C>TCA4651652NAT2c.589C>T (p.Arg197Ter)
c.199C>T (p.Arg67Ter)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.18400593G>ACA114447NAT2c.590G>A (p.Arg197Gln)
c.200G>A (p.Arg67Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.18400593G>CCA370636214NAT2c.590G>C (p.Arg197Pro)
c.200G>C (p.Arg67Pro)
dbSNP gnomAD v3 gnomAD v4
8g.18400593G=CA1768219056NAT2c.590G= (p.Arg197=)
c.200G= (p.Arg67=)
8g.18400593G>TCA370636215NAT2c.590G>T (p.Arg197Leu)
c.200G>T (p.Arg67Leu)
gnomAD v4
8g.18400594A>CCA459881276NAT2c.591A>C (p.Arg197=)
c.201A>C (p.Arg67=)
8g.18400594A>GCA459881277NAT2c.591A>G (p.Arg197=)
c.201A>G (p.Arg67=)

Number of alleles fetched