Chr Mutation (hg38) CAid Gene Transcript Linkouts
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)
5g.132313745A>GCA3403455MIR3936HG,SLC22A4c.629A>G (p.Asn210Ser)
n.433A>G
n.825-1492T>C
c.101A>G (p.Asn34Ser)
c.525A>G (p.Gln175=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.132313745A>TCA360804100MIR3936HG,SLC22A4c.629A>T (p.Asn210Ile)
n.433A>T
n.825-1492T>A
c.101A>T (p.Asn34Ile)
c.525A>T (p.Gln175His)
5g.132313746C>ACA360804101MIR3936HG,SLC22A4c.630C>A (p.Asn210Lys)
n.434C>A
n.825-1493G>T
c.102C>A (p.Asn34Lys)
c.526C>A (p.Leu176Ile)
5g.132313746C=CA1583118477MIR3936HG,SLC22A4c.630C= (p.Asn210=)
n.434C=
n.825-1493G=
c.102C= (p.Asn34=)
c.526C= (p.Leu176=)
5g.132313746C>GCA3403457MIR3936HG,SLC22A4c.630C>G (p.Asn210Lys)
n.434C>G
n.825-1493G>C
c.102C>G (p.Asn34Lys)
c.526C>G (p.Leu176Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.132313746C>TCA3403456MIR3936HG,SLC22A4c.630C>T (p.Asn210=)
n.434C>T
n.825-1493G>A
c.102C>T (p.Asn34=)
c.526C>T (p.Leu176=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.132313747T>ACA360804102MIR3936HG,SLC22A4c.631T>A (p.Tyr211Asn)
n.435T>A
n.825-1494A>T
c.103T>A (p.Tyr35Asn)
c.527T>A (p.Leu176Gln)
5g.132313747T>CCA360804103MIR3936HG,SLC22A4c.631T>C (p.Tyr211His)
n.435T>C
n.825-1494A>G
c.103T>C (p.Tyr35His)
c.527T>C (p.Leu176Pro)
5g.132313747T>GCA360804104MIR3936HG,SLC22A4c.631T>G (p.Tyr211Asp)
n.435T>G
n.825-1494A>C
c.103T>G (p.Tyr35Asp)
c.527T>G (p.Leu176Arg)
5g.132313748A=CA1583118480MIR3936HG,SLC22A4c.632A= (p.Tyr211=)
n.436A=
n.825-1495T=
c.104A= (p.Tyr35=)
c.528A= (p.Leu176=)
5g.132313748A>CCA360804105MIR3936HG,SLC22A4c.632A>C (p.Tyr211Ser)
n.436A>C
n.825-1495T>G
c.104A>C (p.Tyr35Ser)
c.528A>C (p.Leu176=)
5g.132313748A>GCA360804106MIR3936HG,SLC22A4c.632A>G (p.Tyr211Cys)
n.436A>G
n.825-1495T>C
c.104A>G (p.Tyr35Cys)
c.528A>G (p.Leu176=)
 dbSNP gnomAD v3 gnomAD v4
5g.132313748A>TCA360804107MIR3936HG,SLC22A4c.632A>T (p.Tyr211Phe)
n.436A>T
n.825-1495T>A
c.104A>T (p.Tyr35Phe)
c.528A>T (p.Leu176=)
5g.132313749T>ACA360804108MIR3936HG,SLC22A4c.633T>A (p.Tyr211Ter)
n.437T>A
n.825-1496A>T
c.105T>A (p.Tyr35Ter)
c.529T>A (p.Cys177Ser)
5g.132313749T>CCA3403458MIR3936HG,SLC22A4c.633T>C (p.Tyr211=)
n.437T>C
n.825-1496A>G
c.105T>C (p.Tyr35=)
c.529T>C (p.Cys177Arg)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.132313749T>GCA360804110MIR3936HG,SLC22A4c.633T>G (p.Tyr211Ter)
n.437T>G
n.825-1496A>C
c.105T>G (p.Tyr35Ter)
c.529T>G (p.Cys177Gly)
5g.132313749T=CA1583118483MIR3936HG,SLC22A4c.633T= (p.Tyr211=)
n.437T=
n.825-1496A=
c.105T= (p.Tyr35=)
c.529T= (p.Cys177=)
5g.132313750G>ACA3403459MIR3936HG,SLC22A4c.634G>A (p.Val212Met)
n.438G>A
n.825-1497C>T
c.106G>A (p.Val36Met)
c.530G>A (p.Cys177Tyr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.132313750G>CCA360804114MIR3936HG,SLC22A4c.634G>C (p.Val212Leu)
n.438G>C
n.825-1497C>G
c.106G>C (p.Val36Leu)
c.530G>C (p.Cys177Ser)
5g.132313750G=CA1583118485MIR3936HG,SLC22A4c.634G= (p.Val212=)
n.438G=
n.825-1497C=
c.106G= (p.Val36=)
c.530G= (p.Cys177=)

Number of alleles fetched