Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.18400760G>ACA370636563NAT2c.757G>A (p.Val253Ile)
c.367G>A (p.Val123Ile)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.18400760G>CCA370636564NAT2c.757G>C (p.Val253Leu)
c.367G>C (p.Val123Leu)
8g.18400760G=CA1768219135NAT2c.757G= (p.Val253=)
c.367G= (p.Val123=)
8g.18400760G>TCA370636565NAT2c.757G>T (p.Val253Phe)
c.367G>T (p.Val123Phe)
dbSNP gnomAD v4
8g.18400761T>ACA370636566NAT2c.758T>A (p.Val253Asp)
c.368T>A (p.Val123Asp)
8g.18400761T>CCA4651691NAT2c.758T>C (p.Val253Ala)
c.368T>C (p.Val123Ala)
dbSNP ExAC gnomAD v2
8g.18400761T>GCA370636567NAT2c.758T>G (p.Val253Gly)
c.368T>G (p.Val123Gly)
8g.18400761T=CA1768219136NAT2c.758T= (p.Val253=)
c.368T= (p.Val123=)
8g.18400762C>ACA459699616NAT2c.759C>A (p.Val253=)
c.369C>A (p.Val123=)
8g.18400762C=CA1768219137NAT2c.759C= (p.Val253=)
c.369C= (p.Val123=)
8g.18400762C>GCA459699612NAT2c.759C>G (p.Val253=)
c.369C>G (p.Val123=)
8g.18400762C>TCA4651692NAT2c.759C>T (p.Val253=)
c.369C>T (p.Val123=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.18400763G>ACA4651693NAT2c.760G>A (p.Glu254Lys)
c.370G>A (p.Glu124Lys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
8g.18400763G>CCA370636569NAT2c.760G>C (p.Glu254Gln)
c.370G>C (p.Glu124Gln)
dbSNP
8g.18400763G=CA1768219138NAT2c.760G= (p.Glu254=)
c.370G= (p.Glu124=)
8g.18400763G>TCA370636568NAT2c.760G>T (p.Glu254Ter)
c.370G>T (p.Glu124Ter)
gnomAD v4 COSMIC
8g.18400764A>CCA370636570NAT2c.761A>C (p.Glu254Ala)
c.371A>C (p.Glu124Ala)
8g.18400764A>GCA370636572NAT2c.761A>G (p.Glu254Gly)
c.371A>G (p.Glu124Gly)
gnomAD v4
8g.18400764A>TCA370636571NAT2c.761A>T (p.Glu254Val)
c.371A>T (p.Glu124Val)
8g.18400765G>ACA173519942NAT2c.762G>A (p.Glu254=)
c.372G>A (p.Glu124=)
dbSNP
8g.18400765G>CCA370636573NAT2c.762G>C (p.Glu254Asp)
c.372G>C (p.Glu124Asp)
8g.18400765G=CA1768219139NAT2c.762G= (p.Glu254=)
c.372G= (p.Glu124=)
8g.18400765G>TCA370636574NAT2c.762G>T (p.Glu254Asp)
c.372G>T (p.Glu124Asp)
8g.18400765dupCA2539107248NAT2c.762dup (p.Phe255ValfsTer2)
c.372dup (p.Phe125ValfsTer2)
8g.18400766T>ACA370636575NAT2c.763T>A (p.Phe255Ile)
c.373T>A (p.Phe125Ile)
8g.18400766T>CCA370636576NAT2c.763T>C (p.Phe255Leu)
c.373T>C (p.Phe125Leu)
8g.18400766T>GCA370636577NAT2c.763T>G (p.Phe255Val)
c.373T>G (p.Phe125Val)
8g.18400767T>ACA370636578NAT2c.764T>A (p.Phe255Tyr)
c.374T>A (p.Phe125Tyr)
8g.18400767T>CCA370636579NAT2c.764T>C (p.Phe255Ser)
c.374T>C (p.Phe125Ser)
8g.18400767T>GCA370636580NAT2c.764T>G (p.Phe255Cys)
c.374T>G (p.Phe125Cys)
8g.18400767_18400768insCAAGCGTAAACA2550720478NAT2c.764_765insCAAGCGTAAA (p.Thr257ArgfsTer3)
c.374_375insCAAGCGTAAA (p.Thr127ArgfsTer3)
8g.18400768T>ACA370636581NAT2c.765T>A (p.Phe255Leu)
c.375T>A (p.Phe125Leu)
8g.18400768T>CCA459699646NAT2c.765T>C (p.Phe255=)
c.375T>C (p.Phe125=)
8g.18400768T>GCA370636582NAT2c.765T>G (p.Phe255Leu)
c.375T>G (p.Phe125Leu)
gnomAD v3 gnomAD v4
8g.18400769A=CA1768219140NAT2c.766A= (p.Lys256=)
c.376A= (p.Lys126=)
8g.18400769A>CCA370636584NAT2c.766A>C (p.Lys256Gln)
c.376A>C (p.Lys126Gln)
8g.18400769A>GCA4651694NAT2c.766A>G (p.Lys256Glu)
c.376A>G (p.Lys126Glu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.18400769A>TCA370636583NAT2c.766A>T (p.Lys256Ter)
c.376A>T (p.Lys126Ter)
dbSNP gnomAD v2 gnomAD v4
8g.18400770A>CCA370636585NAT2c.767A>C (p.Lys256Thr)
c.377A>C (p.Lys126Thr)
8g.18400770A>GCA370636586NAT2c.767A>G (p.Lys256Arg)
c.377A>G (p.Lys126Arg)
gnomAD v4
8g.18400770A>TCA370636587NAT2c.767A>T (p.Lys256Ile)
c.377A>T (p.Lys126Ile)
8g.18400771A>CCA370636588NAT2c.768A>C (p.Lys256Asn)
c.378A>C (p.Lys126Asn)
gnomAD v4
8g.18400771A>GCA459699661NAT2c.768A>G (p.Lys256=)
c.378A>G (p.Lys126=)
8g.18400771A>TCA370636589NAT2c.768A>T (p.Lys256Asn)
c.378A>T (p.Lys126Asn)
8g.18400772A=CA1768219141NAT2c.769A= (p.Thr257=)
c.379A= (p.Thr127=)
8g.18400772A>CCA370636590NAT2c.769A>C (p.Thr257Pro)
c.379A>C (p.Thr127Pro)
8g.18400772A>GCA4651696NAT2c.769A>G (p.Thr257Ala)
c.379A>G (p.Thr127Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
8g.18400772A>TCA4651695NAT2c.769A>T (p.Thr257Ser)
c.379A>T (p.Thr127Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.18400772_18400774delinsACTCA1768219142NAT2c.769_771delinsACT (p.Thr257=)
c.379_381delinsACT (p.Thr127=)
8g.18400773C>ACA370636591NAT2c.770C>A (p.Thr257Asn)
c.380C>A (p.Thr127Asn)

Number of alleles fetched