Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.132313645A=CA1583118346MIR3936HG,SLC22A4c.529A= (p.Met177=)
n.333A=
n.825-1392T=
c.1A= (p.Met1=)
c.425A= (p.His142=)
5g.132313645A>CCA360803871MIR3936HG,SLC22A4c.529A>C (p.Met177Leu)
n.333A>C
n.825-1392T>G
c.1A>C (p.Met1Leu)
c.425A>C (p.His142Pro)
5g.132313645A>GCA360803872MIR3936HG,SLC22A4c.529A>G (p.Met177Val)
n.333A>G
n.825-1392T>C
c.1A>G (p.Met1Val)
c.425A>G (p.His142Arg)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.132313645A>TCA360803873MIR3936HG,SLC22A4c.529A>T (p.Met177Leu)
n.333A>T
n.825-1392T>A
c.1A>T (p.Met1Leu)
c.425A>T (p.His142Leu)
dbSNP
5g.132313646T>ACA360803874MIR3936HG,SLC22A4c.530T>A (p.Met177Lys)
n.334T>A
n.825-1393A>T
c.2T>A (p.Met1Lys)
c.426T>A (p.His142Gln)
5g.132313646T>CCA360803875MIR3936HG,SLC22A4c.530T>C (p.Met177Thr)
n.334T>C
n.825-1393A>G
c.2T>C (p.Met1Thr)
c.426T>C (p.His142=)
5g.132313646T>GCA360803876MIR3936HG,SLC22A4c.530T>G (p.Met177Arg)
n.334T>G
n.825-1393A>C
c.2T>G (p.Met1Arg)
c.426T>G (p.His142Gln)
5g.132313647G>ACA360803879MIR3936HG,SLC22A4c.531G>A (p.Met177Ile)
n.335G>A
n.825-1394C>T
c.3G>A (p.Met1Ile)
c.427G>A (p.Gly143Ser)
5g.132313647G>CCA360803878MIR3936HG,SLC22A4c.531G>C (p.Met177Ile)
n.335G>C
n.825-1394C>G
c.3G>C (p.Met1Ile)
c.427G>C (p.Gly143Arg)
5g.132313647G>TCA360803877MIR3936HG,SLC22A4c.531G>T (p.Met177Ile)
n.335G>T
n.825-1394C>A
c.3G>T (p.Met1Ile)
c.427G>T (p.Gly143Cys)
5g.132313648G>ACA360803880MIR3936HG,SLC22A4c.532G>A (p.Ala178Thr)
n.336G>A
n.825-1395C>T
c.4G>A (p.Ala2Thr)
c.428G>A (p.Gly143Asp)
gnomAD v4
5g.132313648G>CCA360803881MIR3936HG,SLC22A4c.532G>C (p.Ala178Pro)
n.336G>C
n.825-1395C>G
c.4G>C (p.Ala2Pro)
c.428G>C (p.Gly143Ala)
5g.132313648G>TCA360803882MIR3936HG,SLC22A4c.532G>T (p.Ala178Ser)
n.336G>T
n.825-1395C>A
c.4G>T (p.Ala2Ser)
c.428G>T (p.Gly143Val)
5g.132313649C>ACA360803883MIR3936HG,SLC22A4c.533C>A (p.Ala178Asp)
n.337C>A
n.825-1396G>T
c.5C>A (p.Ala2Asp)
c.429C>A (p.Gly143=)
5g.132313649C>GCA360803884MIR3936HG,SLC22A4c.533C>G (p.Ala178Gly)
n.337C>G
n.825-1396G>C
c.5C>G (p.Ala2Gly)
c.429C>G (p.Gly143=)
5g.132313649C>TCA360803885MIR3936HG,SLC22A4c.533C>T (p.Ala178Val)
n.337C>T
n.825-1396G>A
c.5C>T (p.Ala2Val)
c.429C>T (p.Gly143=)
5g.132313650T>ACA446328518MIR3936HG,SLC22A4c.534T>A (p.Ala178=)
n.338T>A
n.825-1397A>T
c.6T>A (p.Ala2=)
c.430T>A (p.Cys144Ser)
5g.132313650T>CCA3403440MIR3936HG,SLC22A4c.534T>C (p.Ala178=)
n.338T>C
n.825-1397A>G
c.6T>C (p.Ala2=)
c.430T>C (p.Cys144Arg)
dbSNP ExAC gnomAD v2
5g.132313650T>GCA446328521MIR3936HG,SLC22A4c.534T>G (p.Ala178=)
n.338T>G
n.825-1397A>C
c.6T>G (p.Ala2=)
c.430T>G (p.Cys144Gly)
gnomAD v4
5g.132313650T=CA1583118352MIR3936HG,SLC22A4c.534T= (p.Ala178=)
n.338T=
n.825-1397A=
c.6T= (p.Ala2=)
c.430T= (p.Cys144=)
5g.132313651G>ACA3403441MIR3936HG,SLC22A4c.535G>A (p.Val179Ile)
n.339G>A
n.825-1398C>T
c.7G>A (p.Val3Ile)
c.431G>A (p.Cys144Tyr)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.132313651G>CCA360803886MIR3936HG,SLC22A4c.535G>C (p.Val179Leu)
n.339G>C
n.825-1398C>G
c.7G>C (p.Val3Leu)
c.431G>C (p.Cys144Ser)
5g.132313651G=CA1583118356MIR3936HG,SLC22A4c.535G= (p.Val179=)
n.339G=
n.825-1398C=
c.7G= (p.Val3=)
c.431G= (p.Cys144=)
5g.132313651G>TCA360803887MIR3936HG,SLC22A4c.535G>T (p.Val179Leu)
n.339G>T
n.825-1398C>A
c.7G>T (p.Val3Leu)
c.431G>T (p.Cys144Phe)
gnomAD v4
5g.132313652T>ACA360803888MIR3936HG,SLC22A4c.536T>A (p.Val179Glu)
n.340T>A
n.825-1399A>T
c.8T>A (p.Val3Glu)
c.432T>A (p.Cys144Ter)
5g.132313652T>CCA360803889MIR3936HG,SLC22A4c.536T>C (p.Val179Ala)
n.340T>C
n.825-1399A>G
c.8T>C (p.Val3Ala)
c.432T>C (p.Cys144=)
dbSNP gnomAD v2 gnomAD v4
5g.132313652T>GCA360803890MIR3936HG,SLC22A4c.536T>G (p.Val179Gly)
n.340T>G
n.825-1399A>C
c.8T>G (p.Val3Gly)
c.432T>G (p.Cys144Trp)
5g.132313652T=CA1583118360MIR3936HG,SLC22A4c.536T= (p.Val179=)
n.340T=
n.825-1399A=
c.8T= (p.Val3=)
c.432T= (p.Cys144=)
5g.132313653A=CA1583118362MIR3936HG,SLC22A4c.537A= (p.Val179=)
n.341A=
n.825-1400T=
c.9A= (p.Val3=)
c.433A= (p.Thr145=)
5g.132313653A>CCA446328538MIR3936HG,SLC22A4c.537A>C (p.Val179=)
n.341A>C
n.825-1400T>G
c.9A>C (p.Val3=)
c.433A>C (p.Thr145Pro)
5g.132313653A>GCA446328540MIR3936HG,SLC22A4c.537A>G (p.Val179=)
n.341A>G
n.825-1400T>C
c.9A>G (p.Val3=)
c.433A>G (p.Thr145Ala)
dbSNP gnomAD v3 gnomAD v4
5g.132313653A>TCA446328542MIR3936HG,SLC22A4c.537A>T (p.Val179=)
n.341A>T
n.825-1400T>A
c.9A>T (p.Val3=)
c.433A>T (p.Thr145Ser)
5g.132313654C>ACA360803892MIR3936HG,SLC22A4c.538C>A (p.Gln180Lys)
n.342C>A
n.825-1401G>T
c.10C>A (p.Gln4Lys)
c.434C>A (p.Thr145Lys)
5g.132313654C>GCA360803893MIR3936HG,SLC22A4c.538C>G (p.Gln180Glu)
n.342C>G
n.825-1401G>C
c.10C>G (p.Gln4Glu)
c.434C>G (p.Thr145Arg)
5g.132313654C>TCA360803891MIR3936HG,SLC22A4c.538C>T (p.Gln180Ter)
n.342C>T
n.825-1401G>A
c.10C>T (p.Gln4Ter)
c.434C>T (p.Thr145Ile)
5g.132313655A>CCA360803894MIR3936HG,SLC22A4c.539A>C (p.Gln180Pro)
n.343A>C
n.825-1402T>G
c.11A>C (p.Gln4Pro)
c.435A>C (p.Thr145=)
5g.132313655A>GCA360803896MIR3936HG,SLC22A4c.539A>G (p.Gln180Arg)
n.343A>G
n.825-1402T>C
c.11A>G (p.Gln4Arg)
c.435A>G (p.Thr145=)
5g.132313655A>TCA360803895MIR3936HG,SLC22A4c.539A>T (p.Gln180Leu)
n.343A>T
n.825-1402T>A
c.11A>T (p.Gln4Leu)
c.435A>T (p.Thr145=)
5g.132313656G>ACA446328552MIR3936HG,SLC22A4c.540G>A (p.Gln180=)
n.344G>A
n.825-1403C>T
c.12G>A (p.Gln4=)
c.436G>A (p.Asp146Asn)
gnomAD v4
5g.132313656G>CCA127189415MIR3936HG,SLC22A4c.540G>C (p.Gln180His)
n.344G>C
n.825-1403C>G
c.12G>C (p.Gln4His)
c.436G>C (p.Asp146His)
dbSNP
5g.132313656G=CA1583118368MIR3936HG,SLC22A4c.540G= (p.Gln180=)
n.344G=
n.825-1403C=
c.12G= (p.Gln4=)
c.436G= (p.Asp146=)
5g.132313656G>TCA360803897MIR3936HG,SLC22A4c.540G>T (p.Gln180His)
n.344G>T
n.825-1403C>A
c.12G>T (p.Gln4His)
c.436G>T (p.Asp146Tyr)
5g.132313657A>CCA360803898MIR3936HG,SLC22A4c.541A>C (p.Thr181Pro)
n.345A>C
n.825-1404T>G
c.13A>C (p.Thr5Pro)
c.437A>C (p.Asp146Ala)
5g.132313657A>GCA360803899MIR3936HG,SLC22A4c.541A>G (p.Thr181Ala)
n.345A>G
n.825-1404T>C
c.13A>G (p.Thr5Ala)
c.437A>G (p.Asp146Gly)
5g.132313657A>TCA360803900MIR3936HG,SLC22A4c.541A>T (p.Thr181Ser)
n.345A>T
n.825-1404T>A
c.13A>T (p.Thr5Ser)
c.437A>T (p.Asp146Val)
gnomAD v4
5g.132313658C>ACA360803901MIR3936HG,SLC22A4c.542C>A (p.Thr181Asn)
n.346C>A
n.825-1405G>T
c.14C>A (p.Thr5Asn)
c.438C>A (p.Asp146Glu)
5g.132313658C>GCA360803902MIR3936HG,SLC22A4c.542C>G (p.Thr181Ser)
n.346C>G
n.825-1405G>C
c.14C>G (p.Thr5Ser)
c.438C>G (p.Asp146Glu)
5g.132313658C>TCA360803903MIR3936HG,SLC22A4c.542C>T (p.Thr181Ile)
n.346C>T
n.825-1405G>A
c.14C>T (p.Thr5Ile)
c.438C>T (p.Asp146=)
5g.132313659T>ACA446328570MIR3936HG,SLC22A4c.543T>A (p.Thr181=)
n.347T>A
n.825-1406A>T
c.15T>A (p.Thr5=)
c.439T>A (p.Trp147Arg)
5g.132313659T>CCA446328573MIR3936HG,SLC22A4c.543T>C (p.Thr181=)
n.347T>C
n.825-1406A>G
c.15T>C (p.Thr5=)
c.439T>C (p.Trp147Arg)
dbSNP gnomAD v3 gnomAD v4

Number of alleles fetched