Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.18222507G>ACA370445346NAT1c.460G>A (p.Glu154Lys)
c.646G>A (p.Glu216Lys)
n.812G>A
8g.18222507G>CCA370445347NAT1c.460G>C (p.Glu154Gln)
c.646G>C (p.Glu216Gln)
n.812G>C
dbSNP gnomAD v2 gnomAD v4
8g.18222507G=CA1768101188NAT1c.460G= (p.Glu154=)
c.646G= (p.Glu216=)
n.812G=
8g.18222507G>TCA4651417NAT1c.460G>T (p.Glu154Ter)
c.646G>T (p.Glu216Ter)
n.812G>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.18222508A>CCA370445348NAT1c.461A>C (p.Glu154Ala)
c.647A>C (p.Glu216Ala)
n.813A>C
8g.18222508A>GCA370445350NAT1c.461A>G (p.Glu154Gly)
c.647A>G (p.Glu216Gly)
n.813A>G
8g.18222508A>TCA370445349NAT1c.461A>T (p.Glu154Val)
c.647A>T (p.Glu216Val)
n.813A>T
8g.18222509A=CA1768101189NAT1c.462A= (p.Glu154=)
c.648A= (p.Glu216=)
n.814A=
8g.18222509A>CCA370445351NAT1c.462A>C (p.Glu154Asp)
c.648A>C (p.Glu216Asp)
n.814A>C
8g.18222509A>GCA4651418NAT1c.462A>G (p.Glu154=)
c.648A>G (p.Glu216=)
n.814A>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.18222509A>TCA370445352NAT1c.462A>T (p.Glu154Asp)
c.648A>T (p.Glu216Asp)
n.814A>T
8g.18222510G>ACA370445353NAT1c.463G>A (p.Glu155Lys)
c.649G>A (p.Glu217Lys)
n.815G>A
8g.18222510G>CCA370445354NAT1c.463G>C (p.Glu155Gln)
c.649G>C (p.Glu217Gln)
n.815G>C
8g.18222510G>TCA370445355NAT1c.463G>T (p.Glu155Ter)
c.649G>T (p.Glu217Ter)
n.815G>T
gnomAD v4
8g.18222511A>CCA370445356NAT1c.464A>C (p.Glu155Ala)
c.650A>C (p.Glu217Ala)
n.816A>C
8g.18222511A>GCA370445357NAT1c.464A>G (p.Glu155Gly)
c.650A>G (p.Glu217Gly)
n.816A>G
8g.18222511A>TCA370445358NAT1c.464A>T (p.Glu155Val)
c.650A>T (p.Glu217Val)
n.816A>T
8g.18222512G>ACA459877872NAT1c.465G>A (p.Glu155=)
c.651G>A (p.Glu217=)
n.817G>A
8g.18222512G>CCA370445359NAT1c.465G>C (p.Glu155Asp)
c.651G>C (p.Glu217Asp)
n.817G>C
gnomAD v4
8g.18222512G>TCA370445360NAT1c.465G>T (p.Glu155Asp)
c.651G>T (p.Glu217Asp)
n.817G>T
COSMIC COSMIC
8g.18222513A>CCA370445363NAT1c.466A>C (p.Asn156His)
c.652A>C (p.Asn218His)
n.818A>C
8g.18222513A>GCA370445361NAT1c.466A>G (p.Asn156Asp)
c.652A>G (p.Asn218Asp)
n.818A>G
8g.18222513A>TCA370445362NAT1c.466A>T (p.Asn156Tyr)
c.652A>T (p.Asn218Tyr)
n.818A>T
8g.18222514A>CCA370445364NAT1c.467A>C (p.Asn156Thr)
c.653A>C (p.Asn218Thr)
n.819A>C
8g.18222514A>GCA370445366NAT1c.467A>G (p.Asn156Ser)
c.653A>G (p.Asn218Ser)
n.819A>G
8g.18222514A>TCA370445365NAT1c.467A>T (p.Asn156Ile)
c.653A>T (p.Asn218Ile)
n.819A>T
8g.18222515T>ACA370445367NAT1c.468T>A (p.Asn156Lys)
c.654T>A (p.Asn218Lys)
n.820T>A
8g.18222515T>CCA173180390NAT1c.468T>C (p.Asn156=)
c.654T>C (p.Asn218=)
n.820T>C
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.18222515T>GCA370445368NAT1c.468T>G (p.Asn156Lys)
c.654T>G (p.Asn218Lys)
n.820T>G
gnomAD v4
8g.18222515T=CA1768101190NAT1c.468T= (p.Asn156=)
c.654T= (p.Asn218=)
n.820T=
8g.18222516G>ACA370445369NAT1c.469G>A (p.Gly157Arg)
c.655G>A (p.Gly219Arg)
n.821G>A
COSMIC COSMIC
8g.18222516G>CCA370445370NAT1c.469G>C (p.Gly157Arg)
c.655G>C (p.Gly219Arg)
n.821G>C
8g.18222516G=CA1768101191NAT1c.469G= (p.Gly157=)
c.655G= (p.Gly219=)
n.821G=
8g.18222516G>TCA4651419NAT1c.469G>T (p.Gly157Ter)
c.655G>T (p.Gly219Ter)
n.821G>T
dbSNP ExAC gnomAD v2 gnomAD v4
8g.18222517G>ACA370445371NAT1c.470G>A (p.Gly157Glu)
c.656G>A (p.Gly219Glu)
n.822G>A
8g.18222517G>CCA370445373NAT1c.470G>C (p.Gly157Ala)
c.656G>C (p.Gly219Ala)
n.822G>C
8g.18222517G>TCA370445372NAT1c.470G>T (p.Gly157Val)
c.656G>T (p.Gly219Val)
n.822G>T
gnomAD v4
8g.18222518A>CCA459877889NAT1c.471A>C (p.Gly157=)
c.657A>C (p.Gly219=)
n.823A>C
8g.18222518A>GCA459877891NAT1c.471A>G (p.Gly157=)
c.657A>G (p.Gly219=)
n.823A>G
8g.18222518A>TCA459877892NAT1c.471A>T (p.Gly157=)
c.657A>T (p.Gly219=)
n.823A>T
8g.18222519T>ACA370445374NAT1c.472T>A (p.Phe158Ile)
c.658T>A (p.Phe220Ile)
n.824T>A
8g.18222519T>CCA4651420NAT1c.472T>C (p.Phe158Leu)
c.658T>C (p.Phe220Leu)
n.824T>C
dbSNP ExAC gnomAD v2 gnomAD v4
8g.18222519T>GCA370445375NAT1c.472T>G (p.Phe158Val)
c.658T>G (p.Phe220Val)
n.824T>G
8g.18222519T=CA1768101192NAT1c.472T= (p.Phe158=)
c.658T= (p.Phe220=)
n.824T=
8g.18222520T>ACA370445376NAT1c.473T>A (p.Phe158Tyr)
c.659T>A (p.Phe220Tyr)
n.825T>A
dbSNP gnomAD v4
8g.18222520T>CCA370445377NAT1c.473T>C (p.Phe158Ser)
c.659T>C (p.Phe220Ser)
n.825T>C
8g.18222520T>GCA370445378NAT1c.473T>G (p.Phe158Cys)
c.659T>G (p.Phe220Cys)
n.825T>G
8g.18222520T=CA1768101193NAT1c.473T= (p.Phe158=)
c.659T= (p.Phe220=)
n.825T=
8g.18222521C>ACA370445379NAT1c.474C>A (p.Phe158Leu)
c.660C>A (p.Phe220Leu)
n.826C>A
8g.18222521C=CA1768101194NAT1c.474C= (p.Phe158=)
c.660C= (p.Phe220=)
n.826C=

Number of alleles fetched