Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.132313641A>CCA446328495MIR3936HG,SLC22A4c.525A>C (p.Ala175=)
n.329A>C
n.825-1388T>G
c.-4A>C (n.-4A>C)
c.421A>C (p.Asn141His)
5g.132313641A>GCA446328496MIR3936HG,SLC22A4c.525A>G (p.Ala175=)
n.329A>G
n.825-1388T>C
c.-4A>G (n.-4A>G)
c.421A>G (p.Asn141Asp)
5g.132313641A>TCA446328497MIR3936HG,SLC22A4c.525A>T (p.Ala175=)
n.329A>T
n.825-1388T>A
c.-4A>T (n.-4A>T)
c.421A>T (p.Asn141Tyr)
5g.132313642A>CCA360803865MIR3936HG,SLC22A4c.526A>C (p.Thr176Pro)
n.330A>C
n.825-1389T>G
c.-3A>C (n.-3A>C)
c.422A>C (p.Asn141Thr)
5g.132313642A>GCA360803866MIR3936HG,SLC22A4c.526A>G (p.Thr176Ala)
n.330A>G
n.825-1389T>C
c.-3A>G (n.-3A>G)
c.422A>G (p.Asn141Ser)
5g.132313642A>TCA360803867MIR3936HG,SLC22A4c.526A>T (p.Thr176Ser)
n.330A>T
n.825-1389T>A
c.-3A>T (n.-3A>T)
c.422A>T (p.Asn141Ile)
5g.132313643C>ACA360803868MIR3936HG,SLC22A4c.527C>A (p.Thr176Asn)
n.331C>A
n.825-1390G>T
c.-2C>A (n.-2C>A)
c.423C>A (p.Asn141Lys)
5g.132313643C>GCA360803869MIR3936HG,SLC22A4c.527C>G (p.Thr176Ser)
n.331C>G
n.825-1390G>C
c.-2C>G (n.-2C>G)
c.423C>G (p.Asn141Lys)
5g.132313643C>TCA360803870MIR3936HG,SLC22A4c.527C>T (p.Thr176Ile)
n.331C>T
n.825-1390G>A
c.-2C>T (n.-2C>T)
c.423C>T (p.Asn141=)
 gnomAD v4
5g.132313644C>ACA446328506MIR3936HG,SLC22A4c.528C>A (p.Thr176=)
n.332C>A
n.825-1391G>T
c.-1C>A (n.-1C>A)
c.424C>A (p.His142Asn)
5g.132313644C=CA1583118343MIR3936HG,SLC22A4c.528C= (p.Thr176=)
n.332C=
n.825-1391G=
c.-1C= (n.-1C=)
c.424C= (p.His142=)
5g.132313644C>GCA446328504MIR3936HG,SLC22A4c.528C>G (p.Thr176=)
n.332C>G
n.825-1391G>C
c.-1C>G (n.-1C>G)
c.424C>G (p.His142Asp)
5g.132313644C>TCA446328505MIR3936HG,SLC22A4c.528C>T (p.Thr176=)
n.332C>T
n.825-1391G>A
c.-1C>T (n.-1C>T)
c.424C>T (p.His142Tyr)
 dbSNP
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=)

Number of alleles fetched