Chr Mutation (hg38) CAid Gene Transcript Linkouts
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)
8g.18400773C=CA1768219143NAT2c.770C= (p.Thr257=)
c.380C= (p.Thr127=)
8g.18400773C>GCA4651697NAT2c.770C>G (p.Thr257Ser)
c.380C>G (p.Thr127Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
8g.18400773C>TCA370636592NAT2c.770C>T (p.Thr257Ile)
c.380C>T (p.Thr127Ile)
dbSNP gnomAD v3 gnomAD v4
8g.18400776_18400777delCA580502475NAT2c.773_774del (p.Leu258HisfsTer2)
c.383_384del (p.Leu128HisfsTer2)
dbSNP gnomAD v2 gnomAD v4
8g.18400774T>ACA459699679NAT2c.771T>A (p.Thr257=)
c.381T>A (p.Thr127=)
8g.18400774T>CCA459699680NAT2c.771T>C (p.Thr257=)
c.381T>C (p.Thr127=)
8g.18400774T>GCA459699683NAT2c.771T>G (p.Thr257=)
c.381T>G (p.Thr127=)
8g.18400775C>ACA370636594NAT2c.772C>A (p.Leu258Ile)
c.382C>A (p.Leu128Ile)
8g.18400775C=CA1768219144NAT2c.772C= (p.Leu258=)
c.382C= (p.Leu128=)
8g.18400775C>GCA4651698NAT2c.772C>G (p.Leu258Val)
c.382C>G (p.Leu128Val)
dbSNP ExAC gnomAD v2 gnomAD v4
8g.18400775C>TCA370636593NAT2c.772C>T (p.Leu258Phe)
c.382C>T (p.Leu128Phe)
8g.18400776T>ACA370636595NAT2c.773T>A (p.Leu258His)
c.383T>A (p.Leu128His)
8g.18400776T>CCA370636596NAT2c.773T>C (p.Leu258Pro)
c.383T>C (p.Leu128Pro)
gnomAD v4
8g.18400776T>GCA370636597NAT2c.773T>G (p.Leu258Arg)
c.383T>G (p.Leu128Arg)
8g.18400777C>ACA173519943NAT2c.774C>A (p.Leu258=)
c.384C>A (p.Leu128=)
dbSNP gnomAD v4
8g.18400777C=CA1768219145NAT2c.774C= (p.Leu258=)
c.384C= (p.Leu128=)
8g.18400777C>GCA459699695NAT2c.774C>G (p.Leu258=)
c.384C>G (p.Leu128=)
dbSNP
8g.18400777C>TCA459699698NAT2c.774C>T (p.Leu258=)
c.384C>T (p.Leu128=)
8g.18400778A=CA1768219146NAT2c.775A= (p.Thr259=)
c.385A= (p.Thr129=)
8g.18400778A>CCA370636598NAT2c.775A>C (p.Thr259Pro)
c.385A>C (p.Thr129Pro)
gnomAD v4
8g.18400778A>GCA370636599NAT2c.775A>G (p.Thr259Ala)
c.385A>G (p.Thr129Ala)
dbSNP gnomAD v2 gnomAD v4 COSMIC
8g.18400778A>TCA370636600NAT2c.775A>T (p.Thr259Ser)
c.385A>T (p.Thr129Ser)
8g.18400779C>ACA370636601NAT2c.776C>A (p.Thr259Asn)
c.386C>A (p.Thr129Asn)
dbSNP
8g.18400779C=CA1768219147NAT2c.776C= (p.Thr259=)
c.386C= (p.Thr129=)
8g.18400779C>GCA370636602NAT2c.776C>G (p.Thr259Ser)
c.386C>G (p.Thr129Ser)
8g.18400779C>TCA370636603NAT2c.776C>T (p.Thr259Ile)
c.386C>T (p.Thr129Ile)
dbSNP gnomAD v4
8g.18400780T>ACA459699712NAT2c.777T>A (p.Thr259=)
c.387T>A (p.Thr129=)

Number of alleles fetched