Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.132313731G>ACA3403454MIR3936HG,SLC22A4c.615G>A (p.Met205Ile)
n.419G>A
n.825-1478C>T
c.87G>A (p.Met29Ile)
c.511G>A (p.Gly171Arg)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.132313731G>CCA360804068MIR3936HG,SLC22A4c.615G>C (p.Met205Ile)
n.419G>C
n.825-1478C>G
c.87G>C (p.Met29Ile)
c.511G>C (p.Gly171Arg)
5g.132313731G=CA1583118460MIR3936HG,SLC22A4c.615G= (p.Met205=)
n.419G=
n.825-1478C=
c.87G= (p.Met29=)
c.511G= (p.Gly171=)
5g.132313731G>TCA360804067MIR3936HG,SLC22A4c.615G>T (p.Met205Ile)
n.419G>T
n.825-1478C>A
c.87G>T (p.Met29Ile)
c.511G>T (p.Gly171Trp)
5g.132313732G>ACA360804069MIR3936HG,SLC22A4c.616G>A (p.Gly206Ser)
n.420G>A
n.825-1479C>T
c.88G>A (p.Gly30Ser)
c.512G>A (p.Gly171Glu)
5g.132313732G>CCA360804071MIR3936HG,SLC22A4c.616G>C (p.Gly206Arg)
n.420G>C
n.825-1479C>G
c.88G>C (p.Gly30Arg)
c.512G>C (p.Gly171Ala)
5g.132313732G>TCA360804070MIR3936HG,SLC22A4c.616G>T (p.Gly206Cys)
n.420G>T
n.825-1479C>A
c.88G>T (p.Gly30Cys)
c.512G>T (p.Gly171Val)
5g.132313733G>ACA360804072MIR3936HG,SLC22A4c.617G>A (p.Gly206Asp)
n.421G>A
n.825-1480C>T
c.89G>A (p.Gly30Asp)
c.513G>A (p.Gly171=)
5g.132313733G>CCA360804074MIR3936HG,SLC22A4c.617G>C (p.Gly206Ala)
n.421G>C
n.825-1480C>G
c.89G>C (p.Gly30Ala)
c.513G>C (p.Gly171=)
5g.132313733G>TCA360804073MIR3936HG,SLC22A4c.617G>T (p.Gly206Val)
n.421G>T
n.825-1480C>A
c.89G>T (p.Gly30Val)
c.513G>T (p.Gly171=)
5g.132313734C>ACA446328840MIR3936HG,SLC22A4c.618C>A (p.Gly206=)
n.422C>A
n.825-1481G>T
c.90C>A (p.Gly30=)
c.514C>A (p.Pro172Thr)
5g.132313734C>GCA446328842MIR3936HG,SLC22A4c.618C>G (p.Gly206=)
n.422C>G
n.825-1481G>C
c.90C>G (p.Gly30=)
c.514C>G (p.Pro172Ala)
5g.132313734C>TCA446328844MIR3936HG,SLC22A4c.618C>T (p.Gly206=)
n.422C>T
n.825-1481G>A
c.90C>T (p.Gly30=)
c.514C>T (p.Pro172Ser)
5g.132313735C>ACA360804075MIR3936HG,SLC22A4c.619C>A (p.Gln207Lys)
n.423C>A
n.825-1482G>T
c.91C>A (p.Gln31Lys)
c.515C>A (p.Pro172Gln)
5g.132313735C>GCA360804077MIR3936HG,SLC22A4c.619C>G (p.Gln207Glu)
n.423C>G
n.825-1482G>C
c.91C>G (p.Gln31Glu)
c.515C>G (p.Pro172Arg)
5g.132313735C>TCA360804076MIR3936HG,SLC22A4c.619C>T (p.Gln207Ter)
n.423C>T
n.825-1482G>A
c.91C>T (p.Gln31Ter)
c.515C>T (p.Pro172Leu)
5g.132313736A=CA1583118461MIR3936HG,SLC22A4c.620A= (p.Gln207=)
n.424A=
n.825-1483T=
c.92A= (p.Gln31=)
c.516A= (p.Pro172=)
5g.132313736A>CCA360804078MIR3936HG,SLC22A4c.620A>C (p.Gln207Pro)
n.424A>C
n.825-1483T>G
c.92A>C (p.Gln31Pro)
c.516A>C (p.Pro172=)
5g.132313736A>GCA360804079MIR3936HG,SLC22A4c.620A>G (p.Gln207Arg)
n.424A>G
n.825-1483T>C
c.92A>G (p.Gln31Arg)
c.516A>G (p.Pro172=)
dbSNP gnomAD v3 gnomAD v4
5g.132313736A>TCA360804080MIR3936HG,SLC22A4c.620A>T (p.Gln207Leu)
n.424A>T
n.825-1483T>A
c.92A>T (p.Gln31Leu)
c.516A>T (p.Pro172=)
5g.132313737G>ACA446328855MIR3936HG,SLC22A4c.621G>A (p.Gln207=)
n.425G>A
n.825-1484C>T
c.93G>A (p.Gln31=)
c.517G>A (p.Asp173Asn)
5g.132313737G>CCA360804081MIR3936HG,SLC22A4c.621G>C (p.Gln207His)
n.425G>C
n.825-1484C>G
c.93G>C (p.Gln31His)
c.517G>C (p.Asp173His)
5g.132313737G>TCA360804082MIR3936HG,SLC22A4c.621G>T (p.Gln207His)
n.425G>T
n.825-1484C>A
c.93G>T (p.Gln31His)
c.517G>T (p.Asp173Tyr)
5g.132313738A=CA1583118466MIR3936HG,SLC22A4c.622A= (p.Ile208=)
n.426A=
n.825-1485T=
c.94A= (p.Ile32=)
c.518A= (p.Asp173=)
5g.132313738A>CCA360804083MIR3936HG,SLC22A4c.622A>C (p.Ile208Leu)
n.426A>C
n.825-1485T>G
c.94A>C (p.Ile32Leu)
c.518A>C (p.Asp173Ala)
5g.132313738A>GCA360804084MIR3936HG,SLC22A4c.622A>G (p.Ile208Val)
n.426A>G
n.825-1485T>C
c.94A>G (p.Ile32Val)
c.518A>G (p.Asp173Gly)
5g.132313738A>TCA360804085MIR3936HG,SLC22A4c.622A>T (p.Ile208Phe)
n.426A>T
n.825-1485T>A
c.94A>T (p.Ile32Phe)
c.518A>T (p.Asp173Val)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.132313739T>ACA360804086MIR3936HG,SLC22A4c.623T>A (p.Ile208Asn)
n.427T>A
n.825-1486A>T
c.95T>A (p.Ile32Asn)
c.519T>A (p.Asp173Glu)
5g.132313739T>CCA360804087MIR3936HG,SLC22A4c.623T>C (p.Ile208Thr)
n.427T>C
n.825-1486A>G
c.95T>C (p.Ile32Thr)
c.519T>C (p.Asp173=)
dbSNP
5g.132313739T>GCA360804088MIR3936HG,SLC22A4c.623T>G (p.Ile208Ser)
n.427T>G
n.825-1486A>C
c.95T>G (p.Ile32Ser)
c.519T>G (p.Asp173Glu)
5g.132313739T=CA1583118468MIR3936HG,SLC22A4c.623T= (p.Ile208=)
n.427T=
n.825-1486A=
c.95T= (p.Ile32=)
c.519T= (p.Asp173=)
5g.132313740C>ACA446328869MIR3936HG,SLC22A4c.624C>A (p.Ile208=)
n.428C>A
n.825-1487G>T
c.96C>A (p.Ile32=)
c.520C>A (p.Leu174Ile)
5g.132313740C>GCA360804089MIR3936HG,SLC22A4c.624C>G (p.Ile208Met)
n.428C>G
n.825-1487G>C
c.96C>G (p.Ile32Met)
c.520C>G (p.Leu174Val)
5g.132313740C>TCA446328877MIR3936HG,SLC22A4c.624C>T (p.Ile208=)
n.428C>T
n.825-1487G>A
c.96C>T (p.Ile32=)
c.520C>T (p.Leu174Phe)
5g.132313741T>ACA360804090MIR3936HG,SLC22A4c.625T>A (p.Ser209Thr)
n.429T>A
n.825-1488A>T
c.97T>A (p.Ser33Thr)
c.521T>A (p.Leu174His)
5g.132313741T>CCA360804092MIR3936HG,SLC22A4c.625T>C (p.Ser209Pro)
n.429T>C
n.825-1488A>G
c.97T>C (p.Ser33Pro)
c.521T>C (p.Leu174Pro)
5g.132313741T>GCA360804091MIR3936HG,SLC22A4c.625T>G (p.Ser209Ala)
n.429T>G
n.825-1488A>C
c.97T>G (p.Ser33Ala)
c.521T>G (p.Leu174Arg)
5g.132313742C>ACA360804093MIR3936HG,SLC22A4c.626C>A (p.Ser209Tyr)
n.430C>A
n.825-1489G>T
c.98C>A (p.Ser33Tyr)
c.522C>A (p.Leu174=)
dbSNP gnomAD v2
5g.132313742C=CA1583118471MIR3936HG,SLC22A4c.626C= (p.Ser209=)
n.430C=
n.825-1489G=
c.98C= (p.Ser33=)
c.522C= (p.Leu174=)
5g.132313742C>GCA360804094MIR3936HG,SLC22A4c.626C>G (p.Ser209Cys)
n.430C>G
n.825-1489G>C
c.98C>G (p.Ser33Cys)
c.522C>G (p.Leu174=)
5g.132313742C>TCA360804095MIR3936HG,SLC22A4c.626C>T (p.Ser209Phe)
n.430C>T
n.825-1489G>A
c.98C>T (p.Ser33Phe)
c.522C>T (p.Leu174=)
5g.132313743C>ACA446328883MIR3936HG,SLC22A4c.627C>A (p.Ser209=)
n.431C>A
n.825-1490G>T
c.99C>A (p.Ser33=)
c.523C>A (p.Gln175Lys)
5g.132313743C=CA1583118473MIR3936HG,SLC22A4c.627C= (p.Ser209=)
n.431C=
n.825-1490G=
c.99C= (p.Ser33=)
c.523C= (p.Gln175=)
5g.132313743C>GCA446328887MIR3936HG,SLC22A4c.627C>G (p.Ser209=)
n.431C>G
n.825-1490G>C
c.99C>G (p.Ser33=)
c.523C>G (p.Gln175Glu)
5g.132313743C>TCA446328885MIR3936HG,SLC22A4c.627C>T (p.Ser209=)
n.431C>T
n.825-1490G>A
c.99C>T (p.Ser33=)
c.523C>T (p.Gln175Ter)
dbSNP gnomAD v3 gnomAD v4
5g.132313744A>CCA360804096MIR3936HG,SLC22A4c.628A>C (p.Asn210His)
n.432A>C
n.825-1491T>G
c.100A>C (p.Asn34His)
c.524A>C (p.Gln175Pro)
5g.132313744A>GCA360804097MIR3936HG,SLC22A4c.628A>G (p.Asn210Asp)
n.432A>G
n.825-1491T>C
c.100A>G (p.Asn34Asp)
c.524A>G (p.Gln175Arg)
5g.132313744A>TCA360804098MIR3936HG,SLC22A4c.628A>T (p.Asn210Tyr)
n.432A>T
n.825-1491T>A
c.100A>T (p.Asn34Tyr)
c.524A>T (p.Gln175Leu)
5g.132313745A=CA1583118475MIR3936HG,SLC22A4c.629A= (p.Asn210=)
n.433A=
n.825-1492T=
c.101A= (p.Asn34=)
c.525A= (p.Gln175=)
5g.132313745A>CCA360804099MIR3936HG,SLC22A4c.629A>C (p.Asn210Thr)
n.433A>C
n.825-1492T>G
c.101A>C (p.Asn34Thr)
c.525A>C (p.Gln175His)

Number of alleles fetched