Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.124500423_124500505delinsTGGCCCGTGGGCACCGGGCACGGCCATGGGCAGTGCTGGGGCCCCAAAGTCGCCCAGTGGCCCAGCAGGTGGACCGGCGGCCACA1878468864NR5A1c.455_537delinsTGGCCGCCGGTCCACCTGCTGGGCCACTGGGCGACTTTGGGGCCCCAGCACTGCCCATGGCCGTGCCCGGTGCCCACGGGCCA (p.Leu152=)
c.40-233_40-151delinsTGGCCGCCGGTCCACCTGCTGGGCCACTGGGCGACTTTGGGGCCCCAGCACTGCCCATGGCCGTGCCCGGTGCCCACGGGCCA (n.40-233_40-151delinsTGGCCGCCGGTCCACCTGCTGGGCCACTGGGCGACTTTGGGGCCCCAGCACTGCCCATGGCCGTGCCCGGTGCCCACGGGCCA)
c.194_276delinsTGGCCGCCGGTCCACCTGCTGGGCCACTGGGCGACTTTGGGGCCCCAGCACTGCCCATGGCCGTGCCCGGTGCCCACGGGCCA (p.Leu65=)
9g.124500429_124500510delCA915947130NR5A1c.455_536del (p.Leu152HisfsTer?)
c.40-233_40-152del (n.40-233_40-152del)
c.194_275del (p.Leu65HisfsTer?)
ClinVar dbSNP
9g.124500491_124500500delinsGTGGACCGGCCA1878469071NR5A1c.460_469delinsGCCGGTCCAC (p.Ala154=)
c.40-228_40-219delinsGCCGGTCCAC (n.40-228_40-219delinsGCCGGTCCAC)
c.199_208delinsGCCGGTCCAC (p.Ala67=)
9g.124500492_124500500delCA590936669NR5A1c.460_468del (p.Ala154_Pro156del)
c.40-228_40-220del (n.40-228_40-220del)
c.199_207del (p.Ala67_Pro69del)
dbSNP gnomAD v2 gnomAD v4
9g.124500496C>ACA374887705NR5A1c.464G>T (p.Gly155Val)
c.40-224G>T (n.40-224G>T)
c.203G>T (p.Gly68Val)
9g.124500496C=CA1878469089NR5A1c.464G= (p.Gly155=)
c.40-224G= (n.40-224G=)
c.203G= (p.Gly68=)
9g.124500496C>GCA374887698NR5A1c.464G>C (p.Gly155Ala)
c.40-224G>C (n.40-224G>C)
c.203G>C (p.Gly68Ala)
9g.124500496C>TCA374887701NR5A1c.464G>A (p.Gly155Asp)
c.40-224G>A (n.40-224G>A)
c.203G>A (p.Gly68Asp)
dbSNP gnomAD v3 gnomAD v4
9g.124500497C>ACA5235460NR5A1c.463G>T (p.Gly155Cys)
c.40-225G>T (n.40-225G>T)
c.202G>T (p.Gly68Cys)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
9g.124500497C=CA1878469094NR5A1c.463G= (p.Gly155=)
c.40-225G= (n.40-225G=)
c.202G= (p.Gly68=)
9g.124500497C>GCA374887714NR5A1c.463G>C (p.Gly155Arg)
c.40-225G>C (n.40-225G>C)
c.202G>C (p.Gly68Arg)
9g.124500497C>TCA5235461NR5A1c.463G>A (p.Gly155Ser)
c.40-225G>A (n.40-225G>A)
c.202G>A (p.Gly68Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
9g.124500498G>ACA5235462NR5A1c.462C>T (p.Ala154=)
c.40-226C>T (n.40-226C>T)
c.201C>T (p.Ala67=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
9g.124500498G>CCA467208103NR5A1c.462C>G (p.Ala154=)
c.40-226C>G (n.40-226C>G)
c.201C>G (p.Ala67=)
gnomAD v4 COSMIC
9g.124500498G=CA1878469101NR5A1c.462C= (p.Ala154=)
c.40-226C= (n.40-226C=)
c.201C= (p.Ala67=)
9g.124500498G>TCA467208104NR5A1c.462C>A (p.Ala154=)
c.40-226C>A (n.40-226C>A)
c.201C>A (p.Ala67=)
9g.124500499G>ACA374887715NR5A1c.461C>T (p.Ala154Val)
c.40-227C>T (n.40-227C>T)
c.200C>T (p.Ala67Val)
gnomAD v4
9g.124500499G>CCA374887718NR5A1c.461C>G (p.Ala154Gly)
c.40-227C>G (n.40-227C>G)
c.200C>G (p.Ala67Gly)
9g.124500499G>TCA374887720NR5A1c.461C>A (p.Ala154Asp)
c.40-227C>A (n.40-227C>A)
c.200C>A (p.Ala67Asp)
9g.124500500C>ACA374887723NR5A1c.460G>T (p.Ala154Ser)
c.40-228G>T (n.40-228G>T)
c.199G>T (p.Ala67Ser)
dbSNP
9g.124500500C=CA1878469105NR5A1c.460G= (p.Ala154=)
c.40-228G= (n.40-228G=)
c.199G= (p.Ala67=)
9g.124500500C>GCA374887728NR5A1c.460G>C (p.Ala154Pro)
c.40-228G>C (n.40-228G>C)
c.199G>C (p.Ala67Pro)
dbSNP gnomAD v3 gnomAD v4
9g.124500500C>TCA5235463NR5A1c.460G>A (p.Ala154Thr)
c.40-228G>A (n.40-228G>A)
c.199G>A (p.Ala67Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.124500501G>ACA5235464NR5A1c.459C>T (p.Ala153=)
c.40-229C>T (n.40-229C>T)
c.198C>T (p.Ala66=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.124500501G>CCA467208105NR5A1c.459C>G (p.Ala153=)
c.40-229C>G (n.40-229C>G)
c.198C>G (p.Ala66=)
dbSNP gnomAD v4
9g.124500501G=CA1878469113NR5A1c.459C= (p.Ala153=)
c.40-229C= (n.40-229C=)
c.198C= (p.Ala66=)
9g.124500501G>TCA467208106NR5A1c.459C>A (p.Ala153=)
c.40-229C>A (n.40-229C>A)
c.198C>A (p.Ala66=)
gnomAD v4
9g.124500502G>ACA374887745NR5A1c.458C>T (p.Ala153Val)
c.40-230C>T (n.40-230C>T)
c.197C>T (p.Ala66Val)
gnomAD v4
9g.124500502G>CCA374887743NR5A1c.458C>G (p.Ala153Gly)
c.40-230C>G (n.40-230C>G)
c.197C>G (p.Ala66Gly)
9g.124500502G=CA1878469120NR5A1c.458C= (p.Ala153=)
c.40-230C= (n.40-230C=)
c.197C= (p.Ala66=)
9g.124500502G>TCA374887741NR5A1c.458C>A (p.Ala153Asp)
c.40-230C>A (n.40-230C>A)
c.197C>A (p.Ala66Asp)
dbSNP
9g.124500503C>ACA374887747NR5A1c.457G>T (p.Ala153Ser)
c.40-231G>T (n.40-231G>T)
c.196G>T (p.Ala66Ser)
gnomAD v4
9g.124500503C>GCA374887753NR5A1c.457G>C (p.Ala153Pro)
c.40-231G>C (n.40-231G>C)
c.196G>C (p.Ala66Pro)
9g.124500503C>TCA374887749NR5A1c.457G>A (p.Ala153Thr)
c.40-231G>A (n.40-231G>A)
c.196G>A (p.Ala66Thr)
gnomAD v4
9g.124500504C>ACA467208107NR5A1c.456G>T (p.Leu152=)
c.40-232G>T (n.40-232G>T)
c.195G>T (p.Leu65=)
gnomAD v4
9g.124500504C>GCA467208108NR5A1c.456G>C (p.Leu152=)
c.40-232G>C (n.40-232G>C)
c.195G>C (p.Leu65=)
gnomAD v4
9g.124500504C>TCA467208109NR5A1c.456G>A (p.Leu152=)
c.40-232G>A (n.40-232G>A)
c.195G>A (p.Leu65=)
9g.124500505A=CA1878469127NR5A1c.455T= (p.Leu152=)
c.40-233T= (n.40-233T=)
c.194T= (p.Leu65=)
9g.124500505A>CCA374887754NR5A1c.455T>G (p.Leu152Arg)
c.40-233T>G (n.40-233T>G)
c.194T>G (p.Leu65Arg)
9g.124500505A>GCA374887756NR5A1c.455T>C (p.Leu152Pro)
c.40-233T>C (n.40-233T>C)
c.194T>C (p.Leu65Pro)
dbSNP
9g.124500505A>TCA374887755NR5A1c.455T>A (p.Leu152Gln)
c.40-233T>A (n.40-233T>A)
c.194T>A (p.Leu65Gln)
9g.124500506G>ACA467208110NR5A1c.454C>T (p.Leu152=)
c.40-234C>T (n.40-234C>T)
c.193C>T (p.Leu65=)
9g.124500506G>CCA374887758NR5A1c.454C>G (p.Leu152Val)
c.40-234C>G (n.40-234C>G)
c.193C>G (p.Leu65Val)
9g.124500506G>TCA374887759NR5A1c.454C>A (p.Leu152Met)
c.40-234C>A (n.40-234C>A)
c.193C>A (p.Leu65Met)
9g.124500507G>ACA467208113NR5A1c.453C>T (p.Gly151=)
c.40-235C>T (n.40-235C>T)
c.192C>T (p.Gly64=)
dbSNP
9g.124500507G>CCA467208112NR5A1c.453C>G (p.Gly151=)
c.40-235C>G (n.40-235C>G)
c.192C>G (p.Gly64=)
9g.124500507G=CA1878469131NR5A1c.453C= (p.Gly151=)
c.40-235C= (n.40-235C=)
c.192C= (p.Gly64=)
9g.124500507G>TCA467208111NR5A1c.453C>A (p.Gly151=)
c.40-235C>A (n.40-235C>A)
c.192C>A (p.Gly64=)
9g.124500508C>ACA374887761NR5A1c.452G>T (p.Gly151Val)
c.40-236G>T (n.40-236G>T)
c.191G>T (p.Gly64Val)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.124500508C=CA1878469136NR5A1c.452G= (p.Gly151=)
c.40-236G= (n.40-236G=)
c.191G= (p.Gly64=)

Number of alleles fetched