Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.18400860G>ACA114453NAT2c.857G>A (p.Gly286Glu)
c.467G>A (p.Gly156Glu)
ClinVar dbSNP ExAC gnomAD
8g.18400860G>CCA370636771NAT2c.857G>C (p.Gly286Ala)
c.467G>C (p.Gly156Ala)
8g.18400860G=CA1768219186NAT2c.857G= (p.Gly286=)
c.467G= (p.Gly156=)
8g.18400860G>TCA370636772NAT2c.857G>T (p.Gly286Val)
c.467G>T (p.Gly156Val)
8g.18400861A=CA1768219187NAT2c.858A= (p.Gly286=)
c.468A= (p.Gly156=)
8g.18400861A>CCA459700137NAT2c.858A>C (p.Gly286=)
c.468A>C (p.Gly156=)
8g.18400861A>GCA459700139NAT2c.858A>G (p.Gly286=)
c.468A>G (p.Gly156=)
gnomAD
8g.18400861A>TCA459700142NAT2c.858A>T (p.Gly286=)
c.468A>T (p.Gly156=)
8g.18400862T>ACA370636773NAT2c.859T>A (p.Ser287Thr)
c.469T>A (p.Ser157Thr)
8g.18400862T>CCA4651715NAT2c.859T>C (p.Ser287Pro)
c.469T>C (p.Ser157Pro)
dbSNP ExAC
8g.18400862T>GCA370636774NAT2c.859T>G (p.Ser287Ala)
c.469T>G (p.Ser157Ala)
8g.18400862T=CA1768219188NAT2c.859T= (p.Ser287=)
c.469T= (p.Ser157=)
8g.18400863C>ACA370636775NAT2c.860C>A (p.Ser287Tyr)
c.470C>A (p.Ser157Tyr)
8g.18400863C=CA1768219189NAT2c.860C= (p.Ser287=)
c.470C= (p.Ser157=)
8g.18400863C>GCA370636776NAT2c.860C>G (p.Ser287Cys)
c.470C>G (p.Ser157Cys)
gnomAD
8g.18400863C>TCA370636777NAT2c.860C>T (p.Ser287Phe)
c.470C>T (p.Ser157Phe)
COSMIC
8g.18400864C>ACA459700154NAT2c.861C>A (p.Ser287=)
c.471C>A (p.Ser157=)
8g.18400864C=CA1768219190NAT2c.861C= (p.Ser287=)
c.471C= (p.Ser157=)
8g.18400864C>GCA459700156NAT2c.861C>G (p.Ser287=)
c.471C>G (p.Ser157=)
8g.18400864C>TCA4651716NAT2c.861C>T (p.Ser287=)
c.471C>T (p.Ser157=)
dbSNP ExAC gnomAD
8g.18400865C>ACA370636778NAT2c.862C>A (p.Leu288Ile)
c.472C>A (p.Leu158Ile)
8g.18400865C>GCA370636779NAT2c.862C>G (p.Leu288Val)
c.472C>G (p.Leu158Val)
8g.18400865C>TCA370636780NAT2c.862C>T (p.Leu288Phe)
c.472C>T (p.Leu158Phe)
8g.18400866T>ACA370636781NAT2c.863T>A (p.Leu288His)
c.473T>A (p.Leu158His)
8g.18400866T>CCA370636782NAT2c.863T>C (p.Leu288Pro)
c.473T>C (p.Leu158Pro)
8g.18400866T>GCA370636783NAT2c.863T>G (p.Leu288Arg)
c.473T>G (p.Leu158Arg)
8g.18400867T>ACA459700168NAT2c.864T>A (p.Leu288=)
c.474T>A (p.Leu158=)
8g.18400867T>CCA459700170NAT2c.864T>C (p.Leu288=)
c.474T>C (p.Leu158=)
8g.18400867T>GCA459700172NAT2c.864T>G (p.Leu288=)
c.474T>G (p.Leu158=)
8g.18400868A=CA1768219191NAT2c.865A= (p.Thr289=)
c.475A= (p.Thr159=)
8g.18400868A>CCA370636784NAT2c.865A>C (p.Thr289Pro)
c.475A>C (p.Thr159Pro)
8g.18400868A>GCA370636785NAT2c.865A>G (p.Thr289Ala)
c.475A>G (p.Thr159Ala)
8g.18400868A>TCA370636786NAT2c.865A>T (p.Thr289Ser)
c.475A>T (p.Thr159Ser)
8g.18400869C>ACA370636787NAT2c.866C>A (p.Thr289Asn)
c.476C>A (p.Thr159Asn)
8g.18400869C>GCA370636788NAT2c.866C>G (p.Thr289Ser)
c.476C>G (p.Thr159Ser)
8g.18400869C>TCA370636789NAT2c.866C>T (p.Thr289Ile)
c.476C>T (p.Thr159Ile)
8g.18400870T>ACA459700185NAT2c.867T>A (p.Thr289=)
c.477T>A (p.Thr159=)
8g.18400870T>CCA173519952NAT2c.867T>C (p.Thr289=)
c.477T>C (p.Thr159=)
dbSNP
8g.18400870T>GCA459700188NAT2c.867T>G (p.Thr289=)
c.477T>G (p.Thr159=)
8g.18400870T=CA1768219192NAT2c.867T= (p.Thr289=)
c.477T= (p.Thr159=)
8g.18400871A=CA1768219193NAT2c.868A= (p.Ile290=)
c.478A= (p.Ile160=)
8g.18400871A>CCA370636792NAT2c.868A>C (p.Ile290Leu)
c.478A>C (p.Ile160Leu)
8g.18400871A>GCA370636791NAT2c.868A>G (p.Ile290Val)
c.478A>G (p.Ile160Val)
8g.18400871A>TCA370636790NAT2c.868A>T (p.Ile290Phe)
c.478A>T (p.Ile160Phe)
8g.18400872T>ACA370636793NAT2c.869T>A (p.Ile290Asn)
c.479T>A (p.Ile160Asn)
8g.18400872T>CCA4651717NAT2c.869T>C (p.Ile290Thr)
c.479T>C (p.Ile160Thr)
dbSNP ExAC gnomAD
8g.18400872T>GCA370636794NAT2c.869T>G (p.Ile290Ser)
c.479T>G (p.Ile160Ser)
8g.18400872T=CA1768219194NAT2c.869T= (p.Ile290=)
c.479T= (p.Ile160=)
8g.18400873T>ACA459700199NAT2c.870T>A (p.Ile290=)
c.480T>A (p.Ile160=)
8g.18400873T>CCA459700202NAT2c.870T>C (p.Ile290=)
c.480T>C (p.Ile160=)

Number of alleles fetched