Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.25808998G>ACA2644199749SELENONc.646-97G>A (n.646-97G>A)
c.646-28G>A (n.646-28G>A)
c.748-28G>A (n.748-28G>A)
 gnomAD v4
1g.25808998G>CCA2644199750SELENONc.646-97G>C (n.646-97G>C)
c.646-28G>C (n.646-28G>C)
c.748-28G>C (n.748-28G>C)
 gnomAD v4
1g.25808999C>ACA2742889873SELENONc.646-96C>A (n.646-96C>A)
c.646-27C>A (n.646-27C>A)
c.748-27C>A (n.748-27C>A)
1g.25809000delCA2695675607SELENONc.646-95del (n.646-95del)
c.646-26del (n.646-26del)
c.748-26del (n.748-26del)
 dbSNP
1g.25809002G>ACA2574271267SELENONc.646-93G>A (n.646-93G>A)
c.646-24G>A (n.646-24G>A)
c.748-24G>A (n.748-24G>A)
 gnomAD v4
1g.25809004A=CA1159806116SELENONc.646-91A= (n.646-91A=)
c.646-22A= (n.646-22A=)
c.748-22A= (n.748-22A=)
1g.25809004A>GCA1159806117SELENONc.646-91A>G (n.646-91A>G)
c.646-22A>G (n.646-22A>G)
c.748-22A>G (n.748-22A>G)
 dbSNP
1g.25809004A>TCA2644199752SELENONc.646-91A>T (n.646-91A>T)
c.646-22A>T (n.646-22A>T)
c.748-22A>T (n.748-22A>T)
 gnomAD v4
1g.25809005C=CA1159806118SELENONc.646-90C= (n.646-90C=)
c.646-21C= (n.646-21C=)
c.748-21C= (n.748-21C=)
1g.25809005C>TCA696626SELENONc.646-90C>T (n.646-90C>T)
c.646-21C>T (n.646-21C>T)
c.748-21C>T (n.748-21C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC
1g.25809006G>ACA696627SELENONc.646-89G>A (n.646-89G>A)
c.646-20G>A (n.646-20G>A)
c.748-20G>A (n.748-20G>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.25809006G=CA1159806119SELENONc.646-89G= (n.646-89G=)
c.646-20G= (n.646-20G=)
c.748-20G= (n.748-20G=)
1g.25809006G>TCA521738282SELENONc.646-89G>T (n.646-89G>T)
c.646-20G>T (n.646-20G>T)
c.748-20G>T (n.748-20G>T)
 dbSNP gnomAD v2 gnomAD v4
1g.25809007T>ACA2574271268SELENONc.646-88T>A (n.646-88T>A)
c.646-19T>A (n.646-19T>A)
c.748-19T>A (n.748-19T>A)
1g.25809007T>CCA696628SELENONc.646-88T>C (n.646-88T>C)
c.646-19T>C (n.646-19T>C)
c.748-19T>C (n.748-19T>C)
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.25809007T=CA1159806120SELENONc.646-88T= (n.646-88T=)
c.646-19T= (n.646-19T=)
c.748-19T= (n.748-19T=)
1g.25809008G>ACA2644199755SELENONc.646-87G>A (n.646-87G>A)
c.646-18G>A (n.646-18G>A)
c.748-18G>A (n.748-18G>A)
 gnomAD v4
1g.25809012C=CA1145107027SELENONc.646-83C= (n.646-83C=)
c.646-14C= (n.646-14C=)
c.748-14C= (n.748-14C=)
1g.25809012C>TCA696629SELENONc.646-83C>T (n.646-83C>T)
c.646-14C>T (n.646-14C>T)
c.748-14C>T (n.748-14C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.25809014delCA2573132210SELENONc.646-81del (n.646-81del)
c.646-12del (n.646-12del)
c.748-12del (n.748-12del)
 ClinVar dbSNP
1g.25809013C>GCA2644199756SELENONc.646-82C>G (n.646-82C>G)
c.646-13C>G (n.646-13C>G)
c.748-13C>G (n.748-13C>G)
 gnomAD v4
1g.25809014C=CA1143328089SELENONc.646-81C= (n.646-81C=)
c.646-12C= (n.646-12C=)
c.748-12C= (n.748-12C=)
1g.25809014C>TCA696630SELENONc.646-81C>T (n.646-81C>T)
c.646-12C>T (n.646-12C>T)
c.748-12C>T (n.748-12C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.25809015G>ACA696631SELENONc.646-80G>A (n.646-80G>A)
c.646-11G>A (n.646-11G>A)
c.748-11G>A (n.748-11G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.25809015G=CA1159806121SELENONc.646-80G= (n.646-80G=)
c.646-11G= (n.646-11G=)
c.748-11G= (n.748-11G=)
1g.25809016C=CA1159806122SELENONc.646-79C= (n.646-79C=)
c.646-10C= (n.646-10C=)
c.748-10C= (n.748-10C=)
1g.25809016C>TCA696632SELENONc.646-79C>T (n.646-79C>T)
c.646-10C>T (n.646-10C>T)
c.748-10C>T (n.748-10C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.25809017C>ACA2574271269SELENONc.646-78C>A (n.646-78C>A)
c.646-9C>A (n.646-9C>A)
c.748-9C>A (n.748-9C>A)
1g.25809017C=CA1159806123SELENONc.646-78C= (n.646-78C=)
c.646-9C= (n.646-9C=)
c.748-9C= (n.748-9C=)
1g.25809017C>TCA696633SELENONc.646-78C>T (n.646-78C>T)
c.646-9C>T (n.646-9C>T)
c.748-9C>T (n.748-9C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.25809018G>ACA19698365SELENONc.646-77G>A (n.646-77G>A)
c.646-8G>A (n.646-8G>A)
c.748-8G>A (n.748-8G>A)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.25809018G>CCA2644199757SELENONc.646-77G>C (n.646-77G>C)
c.646-8G>C (n.646-8G>C)
c.748-8G>C (n.748-8G>C)
 gnomAD v4
1g.25809018G=CA1145899418SELENONc.646-77G= (n.646-77G=)
c.646-8G= (n.646-8G=)
c.748-8G= (n.748-8G=)
1g.25809019C>ACA19698368SELENONc.646-76C>A (n.646-76C>A)
c.646-7C>A (n.646-7C>A)
c.748-7C>A (n.748-7C>A)
 dbSNP gnomAD v2 gnomAD v4
1g.25809019C=CA1159806124SELENONc.646-76C= (n.646-76C=)
c.646-7C= (n.646-7C=)
c.748-7C= (n.748-7C=)
1g.25809019C>TCA696634SELENONc.646-76C>T (n.646-76C>T)
c.646-7C>T (n.646-7C>T)
c.748-7C>T (n.748-7C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.25809020C=CA1159806125SELENONc.646-75C= (n.646-75C=)
c.646-6C= (n.646-6C=)
c.748-6C= (n.748-6C=)
1g.25809020C>TCA521738288SELENONc.646-75C>T (n.646-75C>T)
c.646-6C>T (n.646-6C>T)
c.748-6C>T (n.748-6C>T)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.25809021_25809036delinsCCCAGGTCATCATCCACA1159806126SELENONc.646-74_646-59delinsCCCAGGTCATCATCCA (n.646-74_646-59delinsCCCAGGTCATCATCCA)
c.646-5_656delinsCCCAGGTCATCATCCA
c.748-5_758delinsCCCAGGTCATCATCCA
1g.25809022C=CA1159806127SELENONc.646-73C= (n.646-73C=)
c.646-4C= (n.646-4C=)
c.748-4C= (n.748-4C=)
1g.25809022C>GCA696636SELENONc.646-73C>G (n.646-73C>G)
c.646-4C>G (n.646-4C>G)
c.748-4C>G (n.748-4C>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.25809024_25809038delCA696635SELENONc.646-71_646-57del (n.646-71_646-57del)
c.646-2_658del
c.748-2_760del
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.25809024A>CCA339113275SELENONc.646-71A>C (n.646-71A>C)
c.646-2A>C (n.646-2A>C)
c.748-2A>C (n.748-2A>C)
1g.25809024A>GCA339113272SELENONc.646-71A>G (n.646-71A>G)
c.646-2A>G (n.646-2A>G)
c.748-2A>G (n.748-2A>G)
1g.25809024A>TCA339113271SELENONc.646-71A>T (n.646-71A>T)
c.646-2A>T (n.646-2A>T)
c.748-2A>T (n.748-2A>T)
1g.25809025G>ACA339113291SELENONc.646-70G>A (n.646-70G>A)
c.646-1G>A (n.646-1G>A)
c.748-1G>A (n.748-1G>A)
1g.25809025G>CCA339113295SELENONc.646-70G>C (n.646-70G>C)
c.646-1G>C (n.646-1G>C)
c.748-1G>C (n.748-1G>C)
1g.25809025G=CA1159806128SELENONc.646-70G= (n.646-70G=)
c.646-1G= (n.646-1G=)
c.748-1G= (n.748-1G=)
1g.25809025G>TCA339113302SELENONc.646-70G>T (n.646-70G>T)
c.646-1G>T (n.646-1G>T)
c.748-1G>T (n.748-1G>T)
 dbSNP gnomAD v4
1g.25809026G>ACA339113307SELENONc.646-69G>A (n.646-69G>A)
c.646G>A (p.Val216Ile)
c.748G>A (p.Val250Ile)
1g.25809026G>CCA339113308SELENONc.646-69G>C (n.646-69G>C)
c.646G>C (p.Val216Leu)
c.748G>C (p.Val250Leu)
1g.25809026G>TCA339113311SELENONc.646-69G>T (n.646-69G>T)
c.646G>T (p.Val216Phe)
c.748G>T (p.Val250Phe)
1g.25809027T>ACA339113314SELENONc.646-68T>A (n.646-68T>A)
c.647T>A (p.Val216Asp)
c.749T>A (p.Val250Asp)
1g.25809027T>CCA339113317SELENONc.646-68T>C (n.646-68T>C)
c.647T>C (p.Val216Ala)
c.749T>C (p.Val250Ala)
1g.25809027T>GCA339113320SELENONc.646-68T>G (n.646-68T>G)
c.647T>G (p.Val216Gly)
c.749T>G (p.Val250Gly)
1g.25809028C>ACA416759035SELENONc.646-67C>A (n.646-67C>A)
c.648C>A (p.Val216=)
c.750C>A (p.Val250=)
1g.25809028C>GCA416759036SELENONc.646-67C>G (n.646-67C>G)
c.648C>G (p.Val216=)
c.750C>G (p.Val250=)
1g.25809028C>TCA416759037SELENONc.646-67C>T (n.646-67C>T)
c.648C>T (p.Val216=)
c.750C>T (p.Val250=)
1g.25809029A>CCA339113325SELENONc.646-66A>C (n.646-66A>C)
c.649A>C (p.Ile217Leu)
c.751A>C (p.Ile251Leu)
1g.25809029A>GCA339113331SELENONc.646-66A>G (n.646-66A>G)
c.649A>G (p.Ile217Val)
c.751A>G (p.Ile251Val)
1g.25809029A>TCA339113336SELENONc.646-66A>T (n.646-66A>T)
c.649A>T (p.Ile217Phe)
c.751A>T (p.Ile251Phe)
1g.25809029_25809030dupCA2644199759SELENONc.646-66_646-65dup (n.646-66_646-65dup)
c.649_650dup (p.Ile218SerfsTer6)
c.751_752dup (p.Ile252SerfsTer6)
 gnomAD v4
1g.25809030T>ACA339113340SELENONc.646-65T>A (n.646-65T>A)
c.650T>A (p.Ile217Asn)
c.752T>A (p.Ile251Asn)
1g.25809030T>CCA339113338SELENONc.646-65T>C (n.646-65T>C)
c.650T>C (p.Ile217Thr)
c.752T>C (p.Ile251Thr)
1g.25809030T>GCA339113337SELENONc.646-65T>G (n.646-65T>G)
c.650T>G (p.Ile217Ser)
c.752T>G (p.Ile251Ser)
1g.25809031C>ACA416759038SELENONc.646-64C>A (n.646-64C>A)
c.651C>A (p.Ile217=)
c.753C>A (p.Ile251=)
1g.25809031C>GCA339113351SELENONc.646-64C>G (n.646-64C>G)
c.651C>G (p.Ile217Met)
c.753C>G (p.Ile251Met)
1g.25809031C>TCA416759039SELENONc.646-64C>T (n.646-64C>T)
c.651C>T (p.Ile217=)
c.753C>T (p.Ile251=)
1g.25809032A>CCA339113355SELENONc.646-63A>C (n.646-63A>C)
c.652A>C (p.Ile218Leu)
c.754A>C (p.Ile252Leu)
1g.25809032A>GCA339113357SELENONc.646-63A>G (n.646-63A>G)
c.652A>G (p.Ile218Val)
c.754A>G (p.Ile252Val)
 COSMIC
1g.25809032A>TCA339113361SELENONc.646-63A>T (n.646-63A>T)
c.652A>T (p.Ile218Phe)
c.754A>T (p.Ile252Phe)
1g.25809033T>ACA339113364SELENONc.646-62T>A (n.646-62T>A)
c.653T>A (p.Ile218Asn)
c.755T>A (p.Ile252Asn)
1g.25809033T>CCA339113367SELENONc.646-62T>C (n.646-62T>C)
c.653T>C (p.Ile218Thr)
c.755T>C (p.Ile252Thr)
1g.25809033T>GCA696637SELENONc.646-62T>G (n.646-62T>G)
c.653T>G (p.Ile218Ser)
c.755T>G (p.Ile252Ser)
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.25809033T=CA1141096141SELENONc.646-62T= (n.646-62T=)
c.653T= (p.Ile218=)
c.755T= (p.Ile252=)
1g.25809034C>ACA416759040SELENONc.646-61C>A (n.646-61C>A)
c.654C>A (p.Ile218=)
c.756C>A (p.Ile252=)
1g.25809034C>GCA339113368SELENONc.646-61C>G (n.646-61C>G)
c.654C>G (p.Ile218Met)
c.756C>G (p.Ile252Met)
1g.25809034C>TCA416759041SELENONc.646-61C>T (n.646-61C>T)
c.654C>T (p.Ile218=)
c.756C>T (p.Ile252=)
 gnomAD v4
1g.25809035C>ACA339113373SELENONc.646-60C>A (n.646-60C>A)
c.655C>A (p.His219Asn)
c.757C>A (p.His253Asn)
1g.25809035C>GCA339113374SELENONc.646-60C>G (n.646-60C>G)
c.655C>G (p.His219Asp)
c.757C>G (p.His253Asp)
1g.25809035C>TCA339113378SELENONc.646-60C>T (n.646-60C>T)
c.655C>T (p.His219Tyr)
c.757C>T (p.His253Tyr)
 gnomAD v4
1g.25809036A>CCA339113382SELENONc.646-59A>C (n.646-59A>C)
c.656A>C (p.His219Pro)
c.758A>C (p.His253Pro)
1g.25809036A>GCA339113385SELENONc.646-59A>G (n.646-59A>G)
c.656A>G (p.His219Arg)
c.758A>G (p.His253Arg)
1g.25809036A>TCA339113389SELENONc.646-59A>T (n.646-59A>T)
c.656A>T (p.His219Leu)
c.758A>T (p.His253Leu)
1g.25809037C>ACA696639SELENONc.646-58C>A (n.646-58C>A)
c.657C>A (p.His219Gln)
c.759C>A (p.His253Gln)
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.25809037C=CA1159806129SELENONc.646-58C= (n.646-58C=)
c.657C= (p.His219=)
c.759C= (p.His253=)
1g.25809037C>GCA339113397SELENONc.646-58C>G (n.646-58C>G)
c.657C>G (p.His219Gln)
c.759C>G (p.His253Gln)
1g.25809037C>TCA696638SELENONc.646-58C>T (n.646-58C>T)
c.657C>T (p.His219=)
c.759C>T (p.His253=)
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
1g.25809038C>ACA416759042SELENONc.646-57C>A (n.646-57C>A)
c.658C>A (p.Arg220=)
c.760C>A (p.Arg254=)
1g.25809038C=CA1143977469SELENONc.646-57C= (n.646-57C=)
c.658C= (p.Arg220=)
c.760C= (p.Arg254=)
1g.25809038C>GCA696641SELENONc.646-57C>G (n.646-57C>G)
c.658C>G (p.Arg220Gly)
c.760C>G (p.Arg254Gly)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.25809038C>TCA696640SELENONc.646-57C>T (n.646-57C>T)
c.658C>T (p.Arg220Trp)
c.760C>T (p.Arg254Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
1g.25809039G>ACA696642SELENONc.646-56G>A (n.646-56G>A)
c.659G>A (p.Arg220Gln)
c.761G>A (p.Arg254Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
1g.25809039G>CCA339113411SELENONc.646-56G>C (n.646-56G>C)
c.659G>C (p.Arg220Pro)
c.761G>C (p.Arg254Pro)
 ClinVar dbSNP
1g.25809039G=CA1159806130SELENONc.646-56G= (n.646-56G=)
c.659G= (p.Arg220=)
c.761G= (p.Arg254=)
1g.25809039G>TCA339113416SELENONc.646-56G>T (n.646-56G>T)
c.659G>T (p.Arg220Leu)
c.761G>T (p.Arg254Leu)
 gnomAD v4
1g.25809040delCA2644199761SELENONc.646-55del (n.646-55del)
c.660del (p.Leu221SerfsTer2)
c.762del (p.Leu255SerfsTer2)
 gnomAD v4
1g.25809040G>ACA416759043SELENONc.646-55G>A (n.646-55G>A)
c.660G>A (p.Arg220=)
c.762G>A (p.Arg254=)
1g.25809040G>CCA416759044SELENONc.646-55G>C (n.646-55G>C)
c.660G>C (p.Arg220=)
c.762G>C (p.Arg254=)
1g.25809040G>TCA416759045SELENONc.646-55G>T (n.646-55G>T)
c.660G>T (p.Arg220=)
c.762G>T (p.Arg254=)
1g.25809041_25809052dupCA1159806131SELENONc.646-54_646-43dup (n.646-54_646-43dup)
c.661_672dup (p.Met224_Phe225insLeuLeuSerMet)
c.763_774dup (p.Met258_Phe259insLeuLeuSerMet)
 dbSNP gnomAD v3 gnomAD v4
1g.25809041C>ACA339113422SELENONc.646-54C>A (n.646-54C>A)
c.661C>A (p.Leu221Ile)
c.763C>A (p.Leu255Ile)
1g.25809041C>GCA339113425SELENONc.646-54C>G (n.646-54C>G)
c.661C>G (p.Leu221Val)
c.763C>G (p.Leu255Val)
1g.25809041C>TCA339113429SELENONc.646-54C>T (n.646-54C>T)
c.661C>T (p.Leu221Phe)
c.763C>T (p.Leu255Phe)
1g.25809042T>ACA339113433SELENONc.646-53T>A (n.646-53T>A)
c.662T>A (p.Leu221His)
c.764T>A (p.Leu255His)
1g.25809042T>CCA339113434SELENONc.646-53T>C (n.646-53T>C)
c.662T>C (p.Leu221Pro)
c.764T>C (p.Leu255Pro)
1g.25809042T>GCA339113435SELENONc.646-53T>G (n.646-53T>G)
c.662T>G (p.Leu221Arg)
c.764T>G (p.Leu255Arg)
1g.25809043C>ACA416759046SELENONc.646-52C>A (n.646-52C>A)
c.663C>A (p.Leu221=)
c.765C>A (p.Leu255=)
1g.25809043C=CA1159806132SELENONc.646-52C= (n.646-52C=)
c.663C= (p.Leu221=)
c.765C= (p.Leu255=)
1g.25809043C>GCA416759048SELENONc.646-52C>G (n.646-52C>G)
c.663C>G (p.Leu221=)
c.765C>G (p.Leu255=)
1g.25809043C>TCA416759047SELENONc.646-52C>T (n.646-52C>T)
c.663C>T (p.Leu221=)
c.765C>T (p.Leu255=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.25809044C>ACA339113436SELENONc.646-51C>A (n.646-51C>A)
c.664C>A (p.Leu222Met)
c.766C>A (p.Leu256Met)
 dbSNP gnomAD v2 gnomAD v4
1g.25809044C=CA1159806133SELENONc.646-51C= (n.646-51C=)
c.664C= (p.Leu222=)
c.766C= (p.Leu256=)
1g.25809044C>GCA339113438SELENONc.646-51C>G (n.646-51C>G)
c.664C>G (p.Leu222Val)
c.766C>G (p.Leu256Val)
1g.25809044C>TCA416759049SELENONc.646-51C>T (n.646-51C>T)
c.664C>T (p.Leu222=)
c.766C>T (p.Leu256=)
 gnomAD v4
1g.25809045T>ACA339113440SELENONc.646-50T>A (n.646-50T>A)
c.665T>A (p.Leu222Gln)
c.767T>A (p.Leu256Gln)
1g.25809045T>CCA339113446SELENONc.646-50T>C (n.646-50T>C)
c.665T>C (p.Leu222Pro)
c.767T>C (p.Leu256Pro)
 gnomAD v4
1g.25809045T>GCA339113442SELENONc.646-50T>G (n.646-50T>G)
c.665T>G (p.Leu222Arg)
c.767T>G (p.Leu256Arg)
1g.25809046G>ACA416759050SELENONc.646-49G>A (n.646-49G>A)
c.666G>A (p.Leu222=)
c.768G>A (p.Leu256=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.25809046G>CCA416759051SELENONc.646-49G>C (n.646-49G>C)
c.666G>C (p.Leu222=)
c.768G>C (p.Leu256=)
1g.25809046G=CA1159806134SELENONc.646-49G= (n.646-49G=)
c.666G= (p.Leu222=)
c.768G= (p.Leu256=)
1g.25809046G>TCA416759052SELENONc.646-49G>T (n.646-49G>T)
c.666G>T (p.Leu222=)
c.768G>T (p.Leu256=)
1g.25809047A>CCA339113463SELENONc.646-48A>C (n.646-48A>C)
c.667A>C (p.Ser223Arg)
c.769A>C (p.Ser257Arg)
 gnomAD v4
1g.25809047A>GCA339113472SELENONc.646-48A>G (n.646-48A>G)
c.667A>G (p.Ser223Gly)
c.769A>G (p.Ser257Gly)
1g.25809047A>TCA339113465SELENONc.646-48A>T (n.646-48A>T)
c.667A>T (p.Ser223Cys)
c.769A>T (p.Ser257Cys)
1g.25809048G>ACA339113478SELENONc.646-47G>A (n.646-47G>A)
c.668G>A (p.Ser223Asn)
c.770G>A (p.Ser257Asn)
 dbSNP gnomAD v2 gnomAD v4
1g.25809048G>CCA339113481SELENONc.646-47G>C (n.646-47G>C)
c.668G>C (p.Ser223Thr)
c.770G>C (p.Ser257Thr)
1g.25809048G=CA1159806135SELENONc.646-47G= (n.646-47G=)
c.668G= (p.Ser223=)
c.770G= (p.Ser257=)
1g.25809048G>TCA339113486SELENONc.646-47G>T (n.646-47G>T)
c.668G>T (p.Ser223Ile)
c.770G>T (p.Ser257Ile)
1g.25809049C>ACA339113487SELENONc.646-46C>A (n.646-46C>A)
c.669C>A (p.Ser223Arg)
c.771C>A (p.Ser257Arg)
1g.25809049C>GCA339113491SELENONc.646-46C>G (n.646-46C>G)
c.669C>G (p.Ser223Arg)
c.771C>G (p.Ser257Arg)
1g.25809049C>TCA416759053SELENONc.646-46C>T (n.646-46C>T)
c.669C>T (p.Ser223=)
c.771C>T (p.Ser257=)
1g.25809050A>CCA339113502SELENONc.646-45A>C (n.646-45A>C)
c.670A>C (p.Met224Leu)
c.772A>C (p.Met258Leu)
 gnomAD v4
1g.25809050A>GCA339113501SELENONc.646-45A>G (n.646-45A>G)
c.670A>G (p.Met224Val)
c.772A>G (p.Met258Val)
 gnomAD v4
1g.25809050A>TCA339113498SELENONc.646-45A>T (n.646-45A>T)
c.670A>T (p.Met224Leu)
c.772A>T (p.Met258Leu)
1g.25809051delCA2580062604SELENONc.646-44del (n.646-44del)
c.671del (p.Met224SerfsTer8)
c.773del (p.Met258SerfsTer8)
 ClinVar
1g.25809051T>ACA339113503SELENONc.646-44T>A (n.646-44T>A)
c.671T>A (p.Met224Lys)
c.773T>A (p.Met258Lys)
1g.25809051T>CCA339113504SELENONc.646-44T>C (n.646-44T>C)
c.671T>C (p.Met224Thr)
c.773T>C (p.Met258Thr)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.25809051T>GCA339113506SELENONc.646-44T>G (n.646-44T>G)
c.671T>G (p.Met224Arg)
c.773T>G (p.Met258Arg)
 dbSNP gnomAD v4
1g.25809051T=CA1159806136SELENONc.646-44T= (n.646-44T=)
c.671T= (p.Met224=)
c.773T= (p.Met258=)
1g.25809052G>ACA339113512SELENONc.646-43G>A (n.646-43G>A)
c.672G>A (p.Met224Ile)
c.774G>A (p.Met258Ile)
1g.25809052G>CCA339113517SELENONc.646-43G>C (n.646-43G>C)
c.672G>C (p.Met224Ile)
c.774G>C (p.Met258Ile)
1g.25809052G=CA1159806137SELENONc.646-43G= (n.646-43G=)
c.672G= (p.Met224=)
c.774G= (p.Met258=)
1g.25809052G>TCA19698381SELENONc.646-43G>T (n.646-43G>T)
c.672G>T (p.Met224Ile)
c.774G>T (p.Met258Ile)
 dbSNP gnomAD v2 gnomAD v4
1g.25809053T>ACA339113526SELENONc.646-42T>A (n.646-42T>A)
c.673T>A (p.Phe225Ile)
c.775T>A (p.Phe259Ile)
1g.25809053T>CCA339113531SELENONc.646-42T>C (n.646-42T>C)
c.673T>C (p.Phe225Leu)
c.775T>C (p.Phe259Leu)
1g.25809053T>GCA339113529SELENONc.646-42T>G (n.646-42T>G)
c.673T>G (p.Phe225Val)
c.775T>G (p.Phe259Val)
1g.25809054T>ACA339113537SELENONc.646-41T>A (n.646-41T>A)
c.674T>A (p.Phe225Tyr)
c.776T>A (p.Phe259Tyr)
1g.25809054T>CCA339113538SELENONc.646-41T>C (n.646-41T>C)
c.674T>C (p.Phe225Ser)
c.776T>C (p.Phe259Ser)
1g.25809054T>GCA339113541SELENONc.646-41T>G (n.646-41T>G)
c.674T>G (p.Phe225Cys)
c.776T>G (p.Phe259Cys)
1g.25809055C>ACA339113545SELENONc.646-40C>A (n.646-40C>A)
c.675C>A (p.Phe225Leu)
c.777C>A (p.Phe259Leu)
1g.25809055C=CA1159806138SELENONc.646-40C= (n.646-40C=)
c.675C= (p.Phe225=)
c.777C= (p.Phe259=)
1g.25809055C>GCA339113549SELENONc.646-40C>G (n.646-40C>G)
c.675C>G (p.Phe225Leu)
c.777C>G (p.Phe259Leu)
 dbSNP
1g.25809055C>TCA416759054SELENONc.646-40C>T (n.646-40C>T)
c.675C>T (p.Phe225=)
c.777C>T (p.Phe259=)
1g.25809056C>ACA339113554SELENONc.646-39C>A (n.646-39C>A)
c.676C>A (p.His226Asn)
c.778C>A (p.His260Asn)
 dbSNP gnomAD v2 gnomAD v4
1g.25809056C=CA1159806139SELENONc.646-39C= (n.646-39C=)
c.676C= (p.His226=)
c.778C= (p.His260=)
1g.25809056C>GCA339113557SELENONc.646-39C>G (n.646-39C>G)
c.676C>G (p.His226Asp)
c.778C>G (p.His260Asp)
1g.25809056C>TCA339113560SELENONc.646-39C>T (n.646-39C>T)
c.676C>T (p.His226Tyr)
c.778C>T (p.His260Tyr)
 gnomAD v4
1g.25809057A>CCA339113563SELENONc.646-38A>C (n.646-38A>C)
c.677A>C (p.His226Pro)
c.779A>C (p.His260Pro)
1g.25809057A>GCA339113566SELENONc.646-38A>G (n.646-38A>G)
c.677A>G (p.His226Arg)
c.779A>G (p.His260Arg)
 COSMIC
1g.25809057A>TCA339113568SELENONc.646-38A>T (n.646-38A>T)
c.677A>T (p.His226Leu)
c.779A>T (p.His260Leu)
1g.25809058C>ACA339113573SELENONc.646-37C>A (n.646-37C>A)
c.678C>A (p.His226Gln)
c.780C>A (p.His260Gln)
1g.25809058C>GCA339113576SELENONc.646-37C>G (n.646-37C>G)
c.678C>G (p.His226Gln)
c.780C>G (p.His260Gln)
1g.25809058C>TCA416759055SELENONc.646-37C>T (n.646-37C>T)
c.678C>T (p.His226=)
c.780C>T (p.His260=)
1g.25809059C>ACA339113582SELENONc.646-36C>A (n.646-36C>A)
c.679C>A (p.Pro227Thr)
c.781C>A (p.Pro261Thr)
1g.25809059C=CA1159806140SELENONc.646-36C= (n.646-36C=)
c.679C= (p.Pro227=)
c.781C= (p.Pro261=)
1g.25809059C>GCA339113585SELENONc.646-36C>G (n.646-36C>G)
c.679C>G (p.Pro227Ala)
c.781C>G (p.Pro261Ala)
1g.25809059C>TCA339113586SELENONc.646-36C>T (n.646-36C>T)
c.679C>T (p.Pro227Ser)
c.781C>T (p.Pro261Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.25809060C>ACA339113590SELENONc.646-35C>A (n.646-35C>A)
c.680C>A (p.Pro227His)
c.782C>A (p.Pro261His)
1g.25809060C>GCA339113591SELENONc.646-35C>G (n.646-35C>G)
c.680C>G (p.Pro227Arg)
c.782C>G (p.Pro261Arg)
1g.25809060C>TCA339113600SELENONc.646-35C>T (n.646-35C>T)
c.680C>T (p.Pro227Leu)
c.782C>T (p.Pro261Leu)
1g.25809061T>ACA416759056SELENONc.646-34T>A (n.646-34T>A)
c.681T>A (p.Pro227=)
c.783T>A (p.Pro261=)
1g.25809061T>CCA416759057SELENONc.646-34T>C (n.646-34T>C)
c.681T>C (p.Pro227=)
c.783T>C (p.Pro261=)
1g.25809061T>GCA416759058SELENONc.646-34T>G (n.646-34T>G)
c.681T>G (p.Pro227=)
c.783T>G (p.Pro261=)
1g.25809062C>ACA416759059SELENONc.646-33C>A (n.646-33C>A)
c.682C>A (p.Arg228=)
c.784C>A (p.Arg262=)
 dbSNP
1g.25809062C=CA1148427826SELENONc.646-33C= (n.646-33C=)
c.682C= (p.Arg228=)
c.784C= (p.Arg262=)
1g.25809062C>GCA339113619SELENONc.646-33C>G (n.646-33C>G)
c.682C>G (p.Arg228Gly)
c.784C>G (p.Arg262Gly)
 ClinVar gnomAD v4
1g.25809062C>TCA696643SELENONc.646-33C>T (n.646-33C>T)
c.682C>T (p.Arg228Trp)
c.784C>T (p.Arg262Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.25809063G>ACA696644SELENONc.646-32G>A (n.646-32G>A)
c.683G>A (p.Arg228Gln)
c.785G>A (p.Arg262Gln)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.25809063G>CCA339113620SELENONc.646-32G>C (n.646-32G>C)
c.683G>C (p.Arg228Pro)
c.785G>C (p.Arg262Pro)
 gnomAD v4
1g.25809063G=CA1159806141SELENONc.646-32G= (n.646-32G=)
c.683G= (p.Arg228=)
c.785G= (p.Arg262=)
1g.25809063G>TCA339113621SELENONc.646-32G>T (n.646-32G>T)
c.683G>T (p.Arg228Leu)
c.785G>T (p.Arg262Leu)
1g.25809064G>ACA416759060SELENONc.646-31G>A (n.646-31G>A)
c.684G>A (p.Arg228=)
c.786G>A (p.Arg262=)
 gnomAD v4
1g.25809064G>CCA416759062SELENONc.646-31G>C (n.646-31G>C)
c.684G>C (p.Arg228=)
c.786G>C (p.Arg262=)
1g.25809064G>TCA416759061SELENONc.646-31G>T (n.646-31G>T)
c.684G>T (p.Arg228=)
c.786G>T (p.Arg262=)
1g.25809065C>ACA339113624SELENONc.646-30C>A (n.646-30C>A)
c.685C>A (p.Pro229Thr)
c.787C>A (p.Pro263Thr)
1g.25809065C>GCA339113628SELENONc.646-30C>G (n.646-30C>G)
c.685C>G (p.Pro229Ala)
c.787C>G (p.Pro263Ala)
1g.25809065C>TCA339113630SELENONc.646-30C>T (n.646-30C>T)
c.685C>T (p.Pro229Ser)
c.787C>T (p.Pro263Ser)
1g.25809066C>ACA339113632SELENONc.646-29C>A (n.646-29C>A)
c.686C>A (p.Pro229His)
c.788C>A (p.Pro263His)
1g.25809066C>GCA339113639SELENONc.646-29C>G (n.646-29C>G)
c.686C>G (p.Pro229Arg)
c.788C>G (p.Pro263Arg)
1g.25809066C>TCA339113636SELENONc.646-29C>T (n.646-29C>T)
c.686C>T (p.Pro229Leu)
c.788C>T (p.Pro263Leu)
1g.25809067C>ACA416759063SELENONc.646-28C>A (n.646-28C>A)
c.687C>A (p.Pro229=)
c.789C>A (p.Pro263=)
1g.25809067C>GCA416759064SELENONc.646-28C>G (n.646-28C>G)
c.687C>G (p.Pro229=)
c.789C>G (p.Pro263=)
1g.25809067C>TCA416759065SELENONc.646-28C>T (n.646-28C>T)
c.687C>T (p.Pro229=)
c.789C>T (p.Pro263=)
1g.25809068T>ACA339113643SELENONc.646-27T>A (n.646-27T>A)
c.688T>A (p.Phe230Ile)
c.790T>A (p.Phe264Ile)
 gnomAD v4
1g.25809068T>CCA339113645SELENONc.646-27T>C (n.646-27T>C)
c.688T>C (p.Phe230Leu)
c.790T>C (p.Phe264Leu)
1g.25809068T>GCA339113651SELENONc.646-27T>G (n.646-27T>G)
c.688T>G (p.Phe230Val)
c.790T>G (p.Phe264Val)
1g.25809069T>ACA339113656SELENONc.646-26T>A (n.646-26T>A)
c.689T>A (p.Phe230Tyr)
c.791T>A (p.Phe264Tyr)
1g.25809069T>CCA339113660SELENONc.646-26T>C (n.646-26T>C)
c.689T>C (p.Phe230Ser)
c.791T>C (p.Phe264Ser)
 dbSNP gnomAD v4
1g.25809069T>GCA339113668SELENONc.646-26T>G (n.646-26T>G)
c.689T>G (p.Phe230Cys)
c.791T>G (p.Phe264Cys)
1g.25809069T=CA1159806142SELENONc.646-26T= (n.646-26T=)
c.689T= (p.Phe230=)
c.791T= (p.Phe264=)
1g.25809070T>ACA339113674SELENONc.646-25T>A (n.646-25T>A)
c.690T>A (p.Phe230Leu)
c.792T>A (p.Phe264Leu)
1g.25809070T>CCA416759066SELENONc.646-25T>C (n.646-25T>C)
c.690T>C (p.Phe230=)
c.792T>C (p.Phe264=)
1g.25809070T>GCA339113677SELENONc.646-25T>G (n.646-25T>G)
c.690T>G (p.Phe230Leu)
c.792T>G (p.Phe264Leu)
1g.25809071G>ACA339113681SELENONc.646-24G>A (n.646-24G>A)
c.691G>A (p.Val231Met)
c.793G>A (p.Val265Met)
 ClinVar dbSNP gnomAD v2 gnomAD v4
1g.25809071G>CCA339113684SELENONc.646-24G>C (n.646-24G>C)
c.691G>C (p.Val231Leu)
c.793G>C (p.Val265Leu)
1g.25809071G=CA1159806143SELENONc.646-24G= (n.646-24G=)
c.691G= (p.Val231=)
c.793G= (p.Val265=)
1g.25809071G>TCA339113690SELENONc.646-24G>T (n.646-24G>T)
c.691G>T (p.Val231Leu)
c.793G>T (p.Val265Leu)
1g.25809072T>ACA696645SELENONc.646-23T>A (n.646-23T>A)
c.692T>A (p.Val231Glu)
c.794T>A (p.Val265Glu)
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.25809072T>CCA339113702SELENONc.646-23T>C (n.646-23T>C)
c.692T>C (p.Val231Ala)
c.794T>C (p.Val265Ala)
1g.25809072T>GCA339113698SELENONc.646-23T>G (n.646-23T>G)
c.692T>G (p.Val231Gly)
c.794T>G (p.Val265Gly)
1g.25809072T=CA1159806144SELENONc.646-23T= (n.646-23T=)
c.692T= (p.Val231=)
c.794T= (p.Val265=)
1g.25809073G>ACA416759067SELENONc.646-22G>A (n.646-22G>A)
c.693G>A (p.Val231=)
c.795G>A (p.Val265=)
 ClinVar
1g.25809073G>CCA416759068SELENONc.646-22G>C (n.646-22G>C)
c.693G>C (p.Val231=)
c.795G>C (p.Val265=)
1g.25809073G>TCA416759069SELENONc.646-22G>T (n.646-22G>T)
c.693G>T (p.Val231=)
c.795G>T (p.Val265=)
1g.25809074A>CCA339113706SELENONc.646-21A>C (n.646-21A>C)
c.694A>C (p.Lys232Gln)
c.796A>C (p.Lys266Gln)
1g.25809074A>GCA339113712SELENONc.646-21A>G (n.646-21A>G)
c.694A>G (p.Lys232Glu)
c.796A>G (p.Lys266Glu)
1g.25809074A>TCA339113709SELENONc.646-21A>T (n.646-21A>T)
c.694A>T (p.Lys232Ter)
c.796A>T (p.Lys266Ter)
1g.25809075A>CCA339113714SELENONc.646-20A>C (n.646-20A>C)
c.695A>C (p.Lys232Thr)
c.797A>C (p.Lys266Thr)
1g.25809075A>GCA339113716SELENONc.646-20A>G (n.646-20A>G)
c.695A>G (p.Lys232Arg)
c.797A>G (p.Lys266Arg)
1g.25809075A>TCA339113719SELENONc.646-20A>T (n.646-20A>T)
c.695A>T (p.Lys232Met)
c.797A>T (p.Lys266Met)
1g.25809076G>ACA416759070SELENONc.646-19G>A (n.646-19G>A)
c.696G>A (p.Lys232=)
c.798G>A (p.Lys266=)
1g.25809076G>CCA339113723SELENONc.646-19G>C (n.646-19G>C)
c.696G>C (p.Lys232Asn)
c.798G>C (p.Lys266Asn)
1g.25809076G>TCA339113724SELENONc.646-19G>T (n.646-19G>T)
c.696G>T (p.Lys232Asn)
c.798G>T (p.Lys266Asn)
1g.25809077A>CCA339113727SELENONc.646-18A>C (n.646-18A>C)
c.697A>C (p.Thr233Pro)
c.799A>C (p.Thr267Pro)
1g.25809077A>GCA339113730SELENONc.646-18A>G (n.646-18A>G)
c.697A>G (p.Thr233Ala)
c.799A>G (p.Thr267Ala)
1g.25809077A>TCA339113731SELENONc.646-18A>T (n.646-18A>T)
c.697A>T (p.Thr233Ser)
c.799A>T (p.Thr267Ser)
1g.25809078C>ACA339113735SELENONc.646-17C>A (n.646-17C>A)
c.698C>A (p.Thr233Asn)
c.800C>A (p.Thr267Asn)
1g.25809078C>GCA339113738SELENONc.646-17C>G (n.646-17C>G)
c.698C>G (p.Thr233Ser)
c.800C>G (p.Thr267Ser)
1g.25809078C>TCA339113740SELENONc.646-17C>T (n.646-17C>T)
c.698C>T (p.Thr233Ile)
c.800C>T (p.Thr267Ile)
1g.25809079C>ACA416759071SELENONc.646-16C>A (n.646-16C>A)
c.699C>A (p.Thr233=)
c.801C>A (p.Thr267=)
1g.25809079C>GCA416759072SELENONc.646-16C>G (n.646-16C>G)
c.699C>G (p.Thr233=)
c.801C>G (p.Thr267=)
 COSMIC
1g.25809079C>TCA416759073SELENONc.646-16C>T (n.646-16C>T)
c.699C>T (p.Thr233=)
c.801C>T (p.Thr267=)
1g.25809080C>ACA339113750SELENONc.646-15C>A (n.646-15C>A)
c.700C>A (p.Arg234Ser)
c.802C>A (p.Arg268Ser)
1g.25809080C=CA1143573366SELENONc.646-15C= (n.646-15C=)
c.700C= (p.Arg234=)
c.802C= (p.Arg268=)
1g.25809080C>GCA339113746SELENONc.646-15C>G (n.646-15C>G)
c.700C>G (p.Arg234Gly)
c.802C>G (p.Arg268Gly)
1g.25809080C>TCA696646SELENONc.646-15C>T (n.646-15C>T)
c.700C>T (p.Arg234Cys)
c.802C>T (p.Arg268Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.25809081G>ACA339113753SELENONc.646-14G>A (n.646-14G>A)
c.701G>A (p.Arg234His)
c.803G>A (p.Arg268His)
 dbSNP gnomAD v4 COSMIC
1g.25809081G>CCA339113756SELENONc.646-14G>C (n.646-14G>C)
c.701G>C (p.Arg234Pro)
c.803G>C (p.Arg268Pro)
1g.25809081G=CA1159806145SELENONc.646-14G= (n.646-14G=)
c.701G= (p.Arg234=)
c.803G= (p.Arg268=)
1g.25809081G>TCA339113760SELENONc.646-14G>T (n.646-14G>T)
c.701G>T (p.Arg234Leu)
c.803G>T (p.Arg268Leu)
 COSMIC
1g.25809082C>ACA416759074SELENONc.646-13C>A (n.646-13C>A)
c.702C>A (p.Arg234=)
c.804C>A (p.Arg268=)
1g.25809082C>GCA416759075SELENONc.646-13C>G (n.646-13C>G)
c.702C>G (p.Arg234=)
c.804C>G (p.Arg268=)
1g.25809082C>TCA416759076SELENONc.646-13C>T (n.646-13C>T)
c.702C>T (p.Arg234=)
c.804C>T (p.Arg268=)
1g.25809083T>ACA339113763SELENONc.646-12T>A (n.646-12T>A)
c.703T>A (p.Phe235Ile)
c.805T>A (p.Phe269Ile)
1g.25809083T>CCA339113770SELENONc.646-12T>C (n.646-12T>C)
c.703T>C (p.Phe235Leu)
c.805T>C (p.Phe269Leu)
 dbSNP gnomAD v2
1g.25809083T>GCA339113771SELENONc.646-12T>G (n.646-12T>G)
c.703T>G (p.Phe235Val)
c.805T>G (p.Phe269Val)
1g.25809083T=CA1159806146SELENONc.646-12T= (n.646-12T=)
c.703T= (p.Phe235=)
c.805T= (p.Phe269=)
1g.25809084T>ACA339113774SELENONc.646-11T>A (n.646-11T>A)
c.704T>A (p.Phe235Tyr)
c.806T>A (p.Phe269Tyr)
1g.25809084T>CCA339113778SELENONc.646-11T>C (n.646-11T>C)
c.704T>C (p.Phe235Ser)
c.806T>C (p.Phe269Ser)
1g.25809084T>GCA339113783SELENONc.646-11T>G (n.646-11T>G)
c.704T>G (p.Phe235Cys)
c.806T>G (p.Phe269Cys)
1g.25809085T>ACA339113786SELENONc.646-10T>A (n.646-10T>A)
c.705T>A (p.Phe235Leu)
c.807T>A (p.Phe269Leu)
1g.25809085T>CCA416759077SELENONc.646-10T>C (n.646-10T>C)
c.705T>C (p.Phe235=)
c.807T>C (p.Phe269=)
1g.25809085T>GCA339113788SELENONc.646-10T>G (n.646-10T>G)
c.705T>G (p.Phe235Leu)
c.807T>G (p.Phe269Leu)
1g.25809086G>ACA696647SELENONc.646-9G>A (n.646-9G>A)
c.706G>A (p.Ala236Thr)
c.808G>A (p.Ala270Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.25809086G>CCA339113791SELENONc.646-9G>C (n.646-9G>C)
c.706G>C (p.Ala236Pro)
c.808G>C (p.Ala270Pro)
1g.25809086G=CA1159806147SELENONc.646-9G= (n.646-9G=)
c.706G= (p.Ala236=)
c.808G= (p.Ala270=)
1g.25809086G>TCA339113789SELENONc.646-9G>T (n.646-9G>T)
c.706G>T (p.Ala236Ser)
c.808G>T (p.Ala270Ser)
1g.25809087C>ACA339113797SELENONc.646-8C>A (n.646-8C>A)
c.707C>A (p.Ala236Asp)
c.809C>A (p.Ala270Asp)
1g.25809087C>GCA339113803SELENONc.646-8C>G (n.646-8C>G)
c.707C>G (p.Ala236Gly)
c.809C>G (p.Ala270Gly)
1g.25809087C>TCA339113805SELENONc.646-8C>T (n.646-8C>T)
c.707C>T (p.Ala236Val)
c.809C>T (p.Ala270Val)
 gnomAD v4
1g.25809088C>ACA416759080SELENONc.646-7C>A (n.646-7C>A)
c.708C>A (p.Ala236=)
c.810C>A (p.Ala270=)
1g.25809088C>GCA416759079SELENONc.646-7C>G (n.646-7C>G)
c.708C>G (p.Ala236=)
c.810C>G (p.Ala270=)
 gnomAD v4
1g.25809088C>TCA416759078SELENONc.646-7C>T (n.646-7C>T)
c.708C>T (p.Ala236=)
c.810C>T (p.Ala270=)
 COSMIC
1g.25809089C>ACA339113809SELENONc.646-6C>A (n.646-6C>A)
c.709C>A (p.Pro237Thr)
c.811C>A (p.Pro271Thr)
1g.25809089C=CA1159806148SELENONc.646-6C= (n.646-6C=)
c.709C= (p.Pro237=)
c.811C= (p.Pro271=)
1g.25809089C>GCA339113814SELENONc.646-6C>G (n.646-6C>G)
c.709C>G (p.Pro237Ala)
c.811C>G (p.Pro271Ala)
1g.25809089C>TCA19698394SELENONc.646-6C>T (n.646-6C>T)
c.709C>T (p.Pro237Ser)
c.811C>T (p.Pro271Ser)
 dbSNP gnomAD v4
1g.25809090C>ACA339113828SELENONc.646-5C>A (n.646-5C>A)
c.710C>A (p.Pro237His)
c.812C>A (p.Pro271His)
1g.25809090C>GCA339113832SELENONc.646-5C>G (n.646-5C>G)
c.710C>G (p.Pro237Arg)
c.812C>G (p.Pro271Arg)
1g.25809090C>TCA339113836SELENONc.646-5C>T (n.646-5C>T)
c.710C>T (p.Pro237Leu)
c.812C>T (p.Pro271Leu)
 gnomAD v4
1g.25809091T>ACA416759081SELENONc.646-4T>A (n.646-4T>A)
c.711T>A (p.Pro237=)
c.813T>A (p.Pro271=)
1g.25809091T>CCA416759083SELENONc.646-4T>C (n.646-4T>C)
c.711T>C (p.Pro237=)
c.813T>C (p.Pro271=)
1g.25809091T>GCA416759082SELENONc.646-4T>G (n.646-4T>G)
c.711T>G (p.Pro237=)
c.813T>G (p.Pro271=)
1g.25809092C>ACA339113851SELENONc.646-3C>A (n.646-3C>A)
c.712C>A (p.Gln238Lys)
c.814C>A (p.Gln272Lys)
1g.25809092C=CA1159806149SELENONc.646-3C= (n.646-3C=)
c.712C= (p.Gln238=)
c.814C= (p.Gln272=)
1g.25809092C>GCA339113852SELENONc.646-3C>G (n.646-3C>G)
c.712C>G (p.Gln238Glu)
c.814C>G (p.Gln272Glu)
 ClinVar dbSNP gnomAD v4
1g.25809092C>TCA339113853SELENONc.646-3C>T (n.646-3C>T)
c.712C>T (p.Gln238Ter)
c.814C>T (p.Gln272Ter)
 ClinVar dbSNP gnomAD v4
1g.25809093A>CCA339113865SELENONc.646-2A>C (n.646-2A>C)
c.713A>C (p.Gln238Pro)
c.815A>C (p.Gln272Pro)
1g.25809093A>GCA339113860SELENONc.646-2A>G (n.646-2A>G)
c.713A>G (p.Gln238Arg)
c.815A>G (p.Gln272Arg)
1g.25809093A>TCA339113857SELENONc.646-2A>T (n.646-2A>T)
c.713A>T (p.Gln238Leu)
c.815A>T (p.Gln272Leu)
1g.25809093_25809094delCA2644199764SELENONc.646-2_646-1del (n.646-2_646-1del)
c.713_714del (p.Gln238ArgfsTer28)
c.815_816del (p.Gln272ArgfsTer28)
 gnomAD v4
1g.25809094G>ACA696648SELENONc.646-1G>A (n.646-1G>A)
c.714G>A (p.Gln238=)
c.816G>A (p.Gln272=)
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.25809094G>CCA339113871SELENONc.646-1G>C (n.646-1G>C)
c.714G>C (p.Gln238His)
c.816G>C (p.Gln272His)
 ClinVar dbSNP gnomAD v4
1g.25809094G=CA1159806150SELENONc.646-1G= (n.646-1G=)
c.714G= (p.Gln238=)
c.816G= (p.Gln272=)
1g.25809094G>TCA339113875SELENONc.646-1G>T (n.646-1G>T)
c.714G>T (p.Gln238His)
c.816G>T (p.Gln272His)
1g.25809095G>ACA339113882SELENONc.646G>A (p.Gly216Arg)
c.715G>A (p.Gly239Arg)
c.817G>A (p.Gly273Arg)
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC
1g.25809095G>CCA339113885SELENONc.646G>C (p.Gly216Arg)
c.715G>C (p.Gly239Arg)
c.817G>C (p.Gly273Arg)
1g.25809095G>TCA339113887SELENONc.646G>T (p.Gly216Ter)
c.715G>T (p.Gly239Ter)
c.817G>T (p.Gly273Ter)
1g.25809096G>ACA253166SELENONc.647G>A (p.Gly216Glu)
c.716G>A (p.Gly239Glu)
c.818G>A (p.Gly273Glu)
 ClinVar dbSNP
1g.25809096G>CCA339113894SELENONc.647G>C (p.Gly216Ala)
c.716G>C (p.Gly239Ala)
c.818G>C (p.Gly273Ala)
1g.25809096G=CA1141580680SELENONc.647G= (p.Gly216=)
c.716G= (p.Gly239=)
c.818G= (p.Gly273=)
1g.25809096G>TCA339113895SELENONc.647G>T (p.Gly216Val)
c.716G>T (p.Gly239Val)
c.818G>T (p.Gly273Val)

Number of alleles fetched