Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.113932282C>ACA2616054429HTR3Bc.369-7C>A (n.369-7C>A)
c.336-7C>A (n.336-7C>A)
c.155-7C>A
c.168-7C>A (n.168-7C>A)
c.162-7C>A (n.162-7C>A)
c.75-7C>A (n.75-7C>A)
n.620-7C>A
 gnomAD v4
11g.113932283A=CA2001397907HTR3Bc.369-6A= (n.369-6A=)
c.336-6A= (n.336-6A=)
c.155-6A=
c.168-6A= (n.168-6A=)
c.162-6A= (n.162-6A=)
c.75-6A= (n.75-6A=)
n.620-6A=
11g.113932283A>GCA6284034HTR3Bc.369-6A>G (n.369-6A>G)
c.336-6A>G (n.336-6A>G)
c.155-6A>G
c.168-6A>G (n.168-6A>G)
c.162-6A>G (n.162-6A>G)
c.75-6A>G (n.75-6A>G)
n.620-6A>G
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.113932284T>CCA2574983877HTR3Bc.369-5T>C (n.369-5T>C)
c.336-5T>C (n.336-5T>C)
c.155-5T>C
c.168-5T>C (n.168-5T>C)
c.162-5T>C (n.162-5T>C)
c.75-5T>C (n.75-5T>C)
n.620-5T>C
 gnomAD v4
11g.113932285A=CA2001397908HTR3Bc.369-4A= (n.369-4A=)
c.336-4A= (n.336-4A=)
c.155-4A=
c.168-4A= (n.168-4A=)
c.162-4A= (n.162-4A=)
c.75-4A= (n.75-4A=)
n.620-4A=
11g.113932285A>CCA2724945732HTR3Bc.369-4A>C (n.369-4A>C)
c.336-4A>C (n.336-4A>C)
c.155-4A>C
c.168-4A>C (n.168-4A>C)
c.162-4A>C (n.162-4A>C)
c.75-4A>C (n.75-4A>C)
n.620-4A>C
 dbSNP
11g.113932285A>GCA2574983878HTR3Bc.369-4A>G (n.369-4A>G)
c.336-4A>G (n.336-4A>G)
c.155-4A>G
c.168-4A>G (n.168-4A>G)
c.162-4A>G (n.162-4A>G)
c.75-4A>G (n.75-4A>G)
n.620-4A>G
11g.113932285A>TCA6284035HTR3Bc.369-4A>T (n.369-4A>T)
c.336-4A>T (n.336-4A>T)
c.155-4A>T
c.168-4A>T (n.168-4A>T)
c.162-4A>T (n.162-4A>T)
c.75-4A>T (n.75-4A>T)
n.620-4A>T
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.113932286T>CCA6284036HTR3Bc.369-3T>C (n.369-3T>C)
c.336-3T>C (n.336-3T>C)
c.155-3T>C
c.168-3T>C (n.168-3T>C)
c.162-3T>C (n.162-3T>C)
c.75-3T>C (n.75-3T>C)
n.620-3T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.113932286T>GCA2616054430HTR3Bc.369-3T>G (n.369-3T>G)
c.336-3T>G (n.336-3T>G)
c.155-3T>G
c.168-3T>G (n.168-3T>G)
c.162-3T>G (n.162-3T>G)
c.75-3T>G (n.75-3T>G)
n.620-3T>G
 gnomAD v4
11g.113932286T=CA2001397909HTR3Bc.369-3T= (n.369-3T=)
c.336-3T= (n.336-3T=)
c.155-3T=
c.168-3T= (n.168-3T=)
c.162-3T= (n.162-3T=)
c.75-3T= (n.75-3T=)
n.620-3T=
11g.113932287A>CCA382668555HTR3Bc.369-2A>C (n.369-2A>C)
c.336-2A>C (n.336-2A>C)
c.155-2A>C
c.168-2A>C (n.168-2A>C)
c.162-2A>C (n.162-2A>C)
c.75-2A>C (n.75-2A>C)
n.620-2A>C
11g.113932287A>GCA382668558HTR3Bc.369-2A>G (n.369-2A>G)
c.336-2A>G (n.336-2A>G)
c.155-2A>G
c.168-2A>G (n.168-2A>G)
c.162-2A>G (n.162-2A>G)
c.75-2A>G (n.75-2A>G)
n.620-2A>G
 gnomAD v4
11g.113932287A>TCA382668559HTR3Bc.369-2A>T (n.369-2A>T)
c.336-2A>T (n.336-2A>T)
c.155-2A>T
c.168-2A>T (n.168-2A>T)
c.162-2A>T (n.162-2A>T)
c.75-2A>T (n.75-2A>T)
n.620-2A>T
11g.113932288G>ACA382668562HTR3Bc.369-1G>A (n.369-1G>A)
c.336-1G>A (n.336-1G>A)
c.155-1G>A
c.168-1G>A (n.168-1G>A)
c.162-1G>A (n.162-1G>A)
c.75-1G>A (n.75-1G>A)
n.620-1G>A
11g.113932288G>CCA382668563HTR3Bc.369-1G>C (n.369-1G>C)
c.336-1G>C (n.336-1G>C)
c.155-1G>C
c.168-1G>C (n.168-1G>C)
c.162-1G>C (n.162-1G>C)
c.75-1G>C (n.75-1G>C)
n.620-1G>C
11g.113932288G>TCA382668565HTR3Bc.369-1G>T (n.369-1G>T)
c.336-1G>T (n.336-1G>T)
c.155-1G>T
c.168-1G>T (n.168-1G>T)
c.162-1G>T (n.162-1G>T)
c.75-1G>T (n.75-1G>T)
n.620-1G>T
11g.113932289T>ACA382668568HTR3Bc.369T>A (p.Phe123Leu)
c.336T>A (p.Phe112Leu)
c.155T>A
c.168T>A (p.Phe56Leu)
c.162T>A (p.Phe54Leu)
c.75T>A (p.Phe25Leu)
n.620T>A
11g.113932289T>CCA476831013HTR3Bc.369T>C (p.Phe123=)
c.336T>C (p.Phe112=)
c.155T>C
c.168T>C (p.Phe56=)
c.162T>C (p.Phe54=)
c.75T>C (p.Phe25=)
n.620T>C
11g.113932289T>GCA382668570HTR3Bc.369T>G (p.Phe123Leu)
c.336T>G (p.Phe112Leu)
c.155T>G
c.168T>G (p.Phe56Leu)
c.162T>G (p.Phe54Leu)
c.75T>G (p.Phe25Leu)
n.620T>G
11g.113932290G>ACA382668573HTR3Bc.370G>A (p.Val124Met)
c.337G>A (p.Val113Met)
c.156G>A
c.169G>A (p.Val57Met)
c.163G>A (p.Val55Met)
c.76G>A (p.Val26Met)
n.621G>A
 dbSNP gnomAD v4
11g.113932290G>CCA382668579HTR3Bc.370G>C (p.Val124Leu)
c.337G>C (p.Val113Leu)
c.156G>C
c.169G>C (p.Val57Leu)
c.163G>C (p.Val55Leu)
c.76G>C (p.Val26Leu)
n.621G>C
11g.113932290G=CA2001397910HTR3Bc.370G= (p.Val124=)
c.337G= (p.Val113=)
c.156G=
c.169G= (p.Val57=)
c.163G= (p.Val55=)
c.76G= (p.Val26=)
n.621G=
11g.113932290G>TCA382668575HTR3Bc.370G>T (p.Val124Leu)
c.337G>T (p.Val113Leu)
c.156G>T
c.169G>T (p.Val57Leu)
c.163G>T (p.Val55Leu)
c.76G>T (p.Val26Leu)
n.621G>T
11g.113932291T>ACA382668581HTR3Bc.371T>A (p.Val124Glu)
c.338T>A (p.Val113Glu)
c.157T>A
c.170T>A (p.Val57Glu)
c.164T>A (p.Val55Glu)
c.77T>A (p.Val26Glu)
n.622T>A
11g.113932291T>CCA382668583HTR3Bc.371T>C (p.Val124Ala)
c.338T>C (p.Val113Ala)
c.157T>C
c.170T>C (p.Val57Ala)
c.164T>C (p.Val55Ala)
c.77T>C (p.Val26Ala)
n.622T>C
11g.113932291T>GCA382668587HTR3Bc.371T>G (p.Val124Gly)
c.338T>G (p.Val113Gly)
c.157T>G
c.170T>G (p.Val57Gly)
c.164T>G (p.Val55Gly)
c.77T>G (p.Val26Gly)
n.622T>G
11g.113932292G>ACA476831025HTR3Bc.372G>A (p.Val124=)
c.339G>A (p.Val113=)
c.158G>A
c.171G>A (p.Val57=)
c.165G>A (p.Val55=)
c.78G>A (p.Val26=)
n.623G>A
11g.113932292G>CCA476831027HTR3Bc.372G>C (p.Val124=)
c.339G>C (p.Val113=)
c.158G>C
c.171G>C (p.Val57=)
c.165G>C (p.Val55=)
c.78G>C (p.Val26=)
n.623G>C
11g.113932292G>TCA476831032HTR3Bc.372G>T (p.Val124=)
c.339G>T (p.Val113=)
c.158G>T
c.171G>T (p.Val57=)
c.165G>T (p.Val55=)
c.78G>T (p.Val26=)
n.623G>T
11g.113932293G>ACA6284037HTR3Bc.373G>A (p.Asp125Asn)
c.340G>A (p.Asp114Asn)
c.159G>A
c.172G>A (p.Asp58Asn)
c.166G>A (p.Asp56Asn)
c.79G>A (p.Asp27Asn)
n.624G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.113932293G>CCA382668590HTR3Bc.373G>C (p.Asp125His)
c.340G>C (p.Asp114His)
c.159G>C
c.172G>C (p.Asp58His)
c.166G>C (p.Asp56His)
c.79G>C (p.Asp27His)
n.624G>C
11g.113932293G=CA2001397911HTR3Bc.373G= (p.Asp125=)
c.340G= (p.Asp114=)
c.159G=
c.172G= (p.Asp58=)
c.166G= (p.Asp56=)
c.79G= (p.Asp27=)
n.624G=
11g.113932293G>TCA382668592HTR3Bc.373G>T (p.Asp125Tyr)
c.340G>T (p.Asp114Tyr)
c.159G>T
c.172G>T (p.Asp58Tyr)
c.166G>T (p.Asp56Tyr)
c.79G>T (p.Asp27Tyr)
n.624G>T
11g.113932294A=CA2001397912HTR3Bc.374A= (p.Asp125=)
c.341A= (p.Asp114=)
c.160A=
c.173A= (p.Asp58=)
c.167A= (p.Asp56=)
c.80A= (p.Asp27=)
n.625A=
11g.113932294A>CCA382668594HTR3Bc.374A>C (p.Asp125Ala)
c.341A>C (p.Asp114Ala)
c.160A>C
c.173A>C (p.Asp58Ala)
c.167A>C (p.Asp56Ala)
c.80A>C (p.Asp27Ala)
n.625A>C
11g.113932294A>GCA382668597HTR3Bc.374A>G (p.Asp125Gly)
c.341A>G (p.Asp114Gly)
c.160A>G
c.173A>G (p.Asp58Gly)
c.167A>G (p.Asp56Gly)
c.80A>G (p.Asp27Gly)
n.625A>G
 dbSNP gnomAD v4
11g.113932294A>TCA382668601HTR3Bc.374A>T (p.Asp125Val)
c.341A>T (p.Asp114Val)
c.160A>T
c.173A>T (p.Asp58Val)
c.167A>T (p.Asp56Val)
c.80A>T (p.Asp27Val)
n.625A>T
11g.113932295C>ACA382668603HTR3Bc.375C>A (p.Asp125Glu)
c.342C>A (p.Asp114Glu)
c.161C>A
c.174C>A (p.Asp58Glu)
c.168C>A (p.Asp56Glu)
c.81C>A (p.Asp27Glu)
n.626C>A
 dbSNP
11g.113932295C>GCA382668605HTR3Bc.375C>G (p.Asp125Glu)
c.342C>G (p.Asp114Glu)
c.161C>G
c.174C>G (p.Asp58Glu)
c.168C>G (p.Asp56Glu)
c.81C>G (p.Asp27Glu)
n.626C>G
11g.113932295C>TCA476831043HTR3Bc.375C>T (p.Asp125=)
c.342C>T (p.Asp114=)
c.161C>T
c.174C>T (p.Asp58=)
c.168C>T (p.Asp56=)
c.81C>T (p.Asp27=)
n.626C>T
 gnomAD v4
11g.113932296A>CCA382668611HTR3Bc.376A>C (p.Ile126Leu)
c.343A>C (p.Ile115Leu)
c.162A>C
c.175A>C (p.Ile59Leu)
c.169A>C (p.Ile57Leu)
c.82A>C (p.Ile28Leu)
n.627A>C
11g.113932296A>GCA382668610HTR3Bc.376A>G (p.Ile126Val)
c.343A>G (p.Ile115Val)
c.162A>G
c.175A>G (p.Ile59Val)
c.169A>G (p.Ile57Val)
c.82A>G (p.Ile28Val)
n.627A>G
 COSMIC COSMIC
11g.113932296A>TCA382668609HTR3Bc.376A>T (p.Ile126Phe)
c.343A>T (p.Ile115Phe)
c.162A>T
c.175A>T (p.Ile59Phe)
c.169A>T (p.Ile57Phe)
c.82A>T (p.Ile28Phe)
n.627A>T
11g.113932297T>ACA382668615HTR3Bc.377T>A (p.Ile126Asn)
c.344T>A (p.Ile115Asn)
c.163T>A
c.176T>A (p.Ile59Asn)
c.170T>A (p.Ile57Asn)
c.83T>A (p.Ile28Asn)
n.628T>A
11g.113932297T>CCA382668612HTR3Bc.377T>C (p.Ile126Thr)
c.344T>C (p.Ile115Thr)
c.163T>C
c.176T>C (p.Ile59Thr)
c.170T>C (p.Ile57Thr)
c.83T>C (p.Ile28Thr)
n.628T>C
 dbSNP gnomAD v3 gnomAD v4
11g.113932297T>GCA382668613HTR3Bc.377T>G (p.Ile126Ser)
c.344T>G (p.Ile115Ser)
c.163T>G
c.176T>G (p.Ile59Ser)
c.170T>G (p.Ile57Ser)
c.83T>G (p.Ile28Ser)
n.628T>G
11g.113932297T=CA2001397913HTR3Bc.377T= (p.Ile126=)
c.344T= (p.Ile115=)
c.163T=
c.176T= (p.Ile59=)
c.170T= (p.Ile57=)
c.83T= (p.Ile28=)
n.628T=
11g.113932298T>ACA476831051HTR3Bc.378T>A (p.Ile126=)
c.345T>A (p.Ile115=)
c.164T>A
c.177T>A (p.Ile59=)
c.171T>A (p.Ile57=)
c.84T>A (p.Ile28=)
n.629T>A
11g.113932298T>CCA476831052HTR3Bc.378T>C (p.Ile126=)
c.345T>C (p.Ile115=)
c.164T>C
c.177T>C (p.Ile59=)
c.171T>C (p.Ile57=)
c.84T>C (p.Ile28=)
n.629T>C
 gnomAD v4

Number of alleles fetched