Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.18400806G>ACA4651704NAT2c.803G>A (p.Arg268Lys)
c.413G>A (p.Arg138Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.18400806G>CCA370636655NAT2c.803G>C (p.Arg268Thr)
c.413G>C (p.Arg138Thr)
 dbSNP gnomAD v4
8g.18400806G=CA114451NAT2c.803G= (p.Arg268=)
c.413G= (p.Arg138=)
8g.18400806G>TCA370636656NAT2c.803G>T (p.Arg268Ile)
c.413G>T (p.Arg138Ile)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.18400807A>CCA370636657NAT2c.804A>C (p.Arg268Ser)
c.414A>C (p.Arg138Ser)
8g.18400807A>GCA459699856NAT2c.804A>G (p.Arg268=)
c.414A>G (p.Arg138=)
8g.18400807A>TCA370636658NAT2c.804A>T (p.Arg268Ser)
c.414A>T (p.Arg138Ser)
8g.18400808A>CCA370636659NAT2c.805A>C (p.Asn269His)
c.415A>C (p.Asn139His)
8g.18400808A>GCA370636660NAT2c.805A>G (p.Asn269Asp)
c.415A>G (p.Asn139Asp)
8g.18400808A>TCA370636661NAT2c.805A>T (p.Asn269Tyr)
c.415A>T (p.Asn139Tyr)
8g.18400809A=CA1768219161NAT2c.806A= (p.Asn269=)
c.416A= (p.Asn139=)
8g.18400809A>CCA370636664NAT2c.806A>C (p.Asn269Thr)
c.416A>C (p.Asn139Thr)
 dbSNP gnomAD v3 gnomAD v4
8g.18400809A>GCA370636663NAT2c.806A>G (p.Asn269Ser)
c.416A>G (p.Asn139Ser)
8g.18400809A>TCA370636662NAT2c.806A>T (p.Asn269Ile)
c.416A>T (p.Asn139Ile)
8g.18400810T>ACA370636665NAT2c.807T>A (p.Asn269Lys)
c.417T>A (p.Asn139Lys)
 dbSNP gnomAD v3 gnomAD v4
8g.18400810T>CCA459699866NAT2c.807T>C (p.Asn269=)
c.417T>C (p.Asn139=)
8g.18400810T>GCA370636666NAT2c.807T>G (p.Asn269Lys)
c.417T>G (p.Asn139Lys)
8g.18400810T=CA1768219162NAT2c.807T= (p.Asn269=)
c.417T= (p.Asn139=)
8g.18400811A>CCA370636667NAT2c.808A>C (p.Ile270Leu)
c.418A>C (p.Ile140Leu)
 gnomAD v4
8g.18400811A>GCA370636668NAT2c.808A>G (p.Ile270Val)
c.418A>G (p.Ile140Val)
8g.18400811A>TCA370636669NAT2c.808A>T (p.Ile270Leu)
c.418A>T (p.Ile140Leu)
8g.18400812T>ACA370636670NAT2c.809T>A (p.Ile270Lys)
c.419T>A (p.Ile140Lys)
8g.18400812T>CCA173519948NAT2c.809T>C (p.Ile270Thr)
c.419T>C (p.Ile140Thr)
 dbSNP gnomAD v2 gnomAD v4
8g.18400812T>GCA370636671NAT2c.809T>G (p.Ile270Arg)
c.419T>G (p.Ile140Arg)
 dbSNP
8g.18400812T=CA1768219163NAT2c.809T= (p.Ile270=)
c.419T= (p.Ile140=)
8g.18400813A=CA1768219164NAT2c.810A= (p.Ile270=)
c.420A= (p.Ile140=)
8g.18400813A>CCA459699879NAT2c.810A>C (p.Ile270=)
c.420A>C (p.Ile140=)
8g.18400813A>GCA370636672NAT2c.810A>G (p.Ile270Met)
c.420A>G (p.Ile140Met)
 dbSNP gnomAD v2 gnomAD v4
8g.18400813A>TCA459699883NAT2c.810A>T (p.Ile270=)
c.420A>T (p.Ile140=)
8g.18400814T>ACA370636673NAT2c.811T>A (p.Phe271Ile)
c.421T>A (p.Phe141Ile)
8g.18400814T>CCA4651705NAT2c.811T>C (p.Phe271Leu)
c.421T>C (p.Phe141Leu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.18400814T>GCA370636674NAT2c.811T>G (p.Phe271Val)
c.421T>G (p.Phe141Val)
8g.18400814T=CA1768219165NAT2c.811T= (p.Phe271=)
c.421T= (p.Phe141=)
8g.18400815T>ACA370636677NAT2c.812T>A (p.Phe271Tyr)
c.422T>A (p.Phe141Tyr)
8g.18400815T>CCA370636676NAT2c.812T>C (p.Phe271Ser)
c.422T>C (p.Phe141Ser)
8g.18400815T>GCA370636675NAT2c.812T>G (p.Phe271Cys)
c.422T>G (p.Phe141Cys)
8g.18400816T>ACA370636678NAT2c.813T>A (p.Phe271Leu)
c.423T>A (p.Phe141Leu)
8g.18400816T>CCA459699893NAT2c.813T>C (p.Phe271=)
c.423T>C (p.Phe141=)
8g.18400816T>GCA370636679NAT2c.813T>G (p.Phe271Leu)
c.423T>G (p.Phe141Leu)
 ClinVar dbSNP gnomAD v3 gnomAD v4
8g.18400816T=CA1768219166NAT2c.813T= (p.Phe271=)
c.423T= (p.Phe141=)
8g.18400817A=CA1768219167NAT2c.814A= (p.Lys272=)
c.424A= (p.Lys142=)
8g.18400817A>CCA370636680NAT2c.814A>C (p.Lys272Gln)
c.424A>C (p.Lys142Gln)
8g.18400817A>GCA370636681NAT2c.814A>G (p.Lys272Glu)
c.424A>G (p.Lys142Glu)
 dbSNP gnomAD v2 gnomAD v4
8g.18400817A>TCA370636682NAT2c.814A>T (p.Lys272Ter)
c.424A>T (p.Lys142Ter)
8g.18400818A>CCA370636683NAT2c.815A>C (p.Lys272Thr)
c.425A>C (p.Lys142Thr)
8g.18400818A>GCA370636684NAT2c.815A>G (p.Lys272Arg)
c.425A>G (p.Lys142Arg)
8g.18400818A>TCA370636685NAT2c.815A>T (p.Lys272Met)
c.425A>T (p.Lys142Met)
8g.18400819G>ACA459699906NAT2c.816G>A (p.Lys272=)
c.426G>A (p.Lys142=)
8g.18400819G>CCA370636686NAT2c.816G>C (p.Lys272Asn)
c.426G>C (p.Lys142Asn)
8g.18400819G>TCA370636687NAT2c.816G>T (p.Lys272Asn)
c.426G>T (p.Lys142Asn)
 COSMIC

Number of alleles fetched