Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.24122868A>CCA2755546932THRBc.*16T>G (n.*16T>G)
c.*2031T>G (n.*2031T>G)
3g.24122870T>GCA71604835THRBc.*14A>C (n.*14A>C)
c.*2029A>C (n.*2029A>C)
dbSNP gnomAD v3 gnomAD v4
3g.24122870T=CA1351822099THRBc.*14A= (n.*14A=)
c.*2029A= (n.*2029A=)
3g.24122871G>ACA2664767998THRBc.*13C>T (n.*13C>T)
c.*2028C>T (n.*2028C>T)
gnomAD v4
3g.24122873A>GCA2577530522THRBc.*11T>C (n.*11T>C)
c.*2026T>C (n.*2026T>C)
gnomAD v4
3g.24122875C>TCA2586965644THRBc.*9G>A (n.*9G>A)
c.*2024G>A (n.*2024G>A)
3g.24122876delCA2755546933THRBc.*9del (n.*9del)
c.*2024del (n.*2024del)
3g.24122876C=CA1351822100THRBc.*8G= (n.*8G=)
c.*2023G= (n.*2023G=)
3g.24122881_24122884delCA2664767999THRBc.*5_*8del (n.*5_*8del)
c.*2020_*2023del (n.*2020_*2023del)
gnomAD v4
3g.24122877_24122879dupCA1045973678THRBc.*5_*7dup (n.*5_*7dup)
c.*2020_*2022dup (n.*2020_*2022dup)
dbSNP gnomAD v3 gnomAD v4
3g.24122880C=CA1351822102THRBc.*4G= (n.*4G=)
c.*2019G= (n.*2019G=)
3g.24122880C>TCA2287075THRBc.*4G>A (n.*4G>A)
c.*2019G>A (n.*2019G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.24122881A>GCA2664768000THRBc.*3T>C (n.*3T>C)
c.*2018T>C (n.*2018T>C)
gnomAD v4
3g.24122882G>ACA2287076THRBc.*2C>T (n.*2C>T)
c.*2017C>T (n.*2017C>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.24122882G>CCA1351822105THRBc.*2C>G (n.*2C>G)
c.*2017C>G (n.*2017C>G)
dbSNP
3g.24122882G=CA1351822104THRBc.*2C= (n.*2C=)
c.*2017C= (n.*2017C=)
3g.24122884C>ACA351886431THRBc.1386G>T (p.Ter462Tyr)
c.*2015G>T (n.*2015G>T)
c.1431G>T (p.Ter477Tyr)
c.1293G>T (p.Ter431Tyr)
c.1215G>T (p.Ter405Tyr)
3g.24122884C=CA1351822106THRBc.1386G= (p.Ter462=)
c.*2015G= (n.*2015G=)
c.1431G= (p.Ter477=)
c.1293G= (p.Ter431=)
c.1215G= (p.Ter405=)
3g.24122884C>GCA351886432THRBc.1386G>C (p.Ter462Tyr)
c.*2015G>C (n.*2015G>C)
c.1431G>C (p.Ter477Tyr)
c.1293G>C (p.Ter431Tyr)
c.1215G>C (p.Ter405Tyr)
dbSNP
3g.24122884C>TCA432903829THRBc.1386G>A (p.Ter462=)
c.*2015G>A (n.*2015G>A)
c.1431G>A (p.Ter477=)
c.1293G>A (p.Ter431=)
c.1215G>A (p.Ter405=)
3g.24122885T>ACA351886435THRBc.1385A>T (p.Ter462Leu)
c.*2014A>T (n.*2014A>T)
c.1430A>T (p.Ter477Leu)
c.1292A>T (p.Ter431Leu)
c.1214A>T (p.Ter405Leu)
3g.24122885T>CCA351886434THRBc.1385A>G (p.Ter462Trp)
c.*2014A>G (n.*2014A>G)
c.1430A>G (p.Ter477Trp)
c.1292A>G (p.Ter431Trp)
c.1214A>G (p.Ter405Trp)
3g.24122885T>GCA351886433THRBc.1385A>C (p.Ter462Ser)
c.*2014A>C (n.*2014A>C)
c.1430A>C (p.Ter477Ser)
c.1292A>C (p.Ter431Ser)
c.1214A>C (p.Ter405Ser)
3g.24122886A>CCA351886436THRBc.1384T>G (p.Ter462Glu)
c.*2013T>G (n.*2013T>G)
c.1429T>G (p.Ter477Glu)
c.1291T>G (p.Ter431Glu)
c.1213T>G (p.Ter405Glu)
3g.24122886A>GCA351886437THRBc.1384T>C (p.Ter462Gln)
c.*2013T>C (n.*2013T>C)
c.1429T>C (p.Ter477Gln)
c.1291T>C (p.Ter431Gln)
c.1213T>C (p.Ter405Gln)
3g.24122886A>TCA351886438THRBc.1384T>A (p.Ter462Lys)
c.*2013T>A (n.*2013T>A)
c.1429T>A (p.Ter477Lys)
c.1291T>A (p.Ter431Lys)
c.1213T>A (p.Ter405Lys)
3g.24122887A>CCA351886439THRBc.1383T>G (p.Asp461Glu)
c.*2012T>G (n.*2012T>G)
c.1428T>G (p.Asp476Glu)
c.1290T>G (p.Asp430Glu)
c.1212T>G (p.Asp404Glu)
3g.24122887A>GCA432903848THRBc.1383T>C (p.Asp461=)
c.*2012T>C (n.*2012T>C)
c.1428T>C (p.Asp476=)
c.1290T>C (p.Asp430=)
c.1212T>C (p.Asp404=)
3g.24122887A>TCA351886440THRBc.1383T>A (p.Asp461Glu)
c.*2012T>A (n.*2012T>A)
c.1428T>A (p.Asp476Glu)
c.1290T>A (p.Asp430Glu)
c.1212T>A (p.Asp404Glu)
3g.24122888T>ACA351886441THRBc.1382A>T (p.Asp461Val)
c.*2011A>T (n.*2011A>T)
c.1427A>T (p.Asp476Val)
c.1289A>T (p.Asp430Val)
c.1211A>T (p.Asp404Val)
3g.24122888T>CCA351886442THRBc.1382A>G (p.Asp461Gly)
c.*2011A>G (n.*2011A>G)
c.1427A>G (p.Asp476Gly)
c.1289A>G (p.Asp430Gly)
c.1211A>G (p.Asp404Gly)
3g.24122888T>GCA351886443THRBc.1382A>C (p.Asp461Ala)
c.*2011A>C (n.*2011A>C)
c.1427A>C (p.Asp476Ala)
c.1289A>C (p.Asp430Ala)
c.1211A>C (p.Asp404Ala)
3g.24122889C>ACA351886444THRBc.1381G>T (p.Asp461Tyr)
c.*2010G>T (n.*2010G>T)
c.1426G>T (p.Asp476Tyr)
c.1288G>T (p.Asp430Tyr)
c.1210G>T (p.Asp404Tyr)
3g.24122889C>GCA351886445THRBc.1381G>C (p.Asp461His)
c.*2010G>C (n.*2010G>C)
c.1426G>C (p.Asp476His)
c.1288G>C (p.Asp430His)
c.1210G>C (p.Asp404His)
3g.24122889C>TCA351886446THRBc.1381G>A (p.Asp461Asn)
c.*2010G>A (n.*2010G>A)
c.1426G>A (p.Asp476Asn)
c.1288G>A (p.Asp430Asn)
c.1210G>A (p.Asp404Asn)
3g.24122890C>ACA351886447THRBc.1380G>T (p.Glu460Asp)
c.*2009G>T (n.*2009G>T)
c.1425G>T (p.Glu475Asp)
c.1287G>T (p.Glu429Asp)
c.1209G>T (p.Glu403Asp)
3g.24122890C=CA1351822107THRBc.1380G= (p.Glu460=)
c.*2009G= (n.*2009G=)
c.1425G= (p.Glu475=)
c.1287G= (p.Glu429=)
c.1209G= (p.Glu403=)
3g.24122890C>GCA351886448THRBc.1380G>C (p.Glu460Asp)
c.*2009G>C (n.*2009G>C)
c.1425G>C (p.Glu475Asp)
c.1287G>C (p.Glu429Asp)
c.1209G>C (p.Glu403Asp)
3g.24122890C>TCA432903871THRBc.1380G>A (p.Glu460=)
c.*2009G>A (n.*2009G>A)
c.1425G>A (p.Glu475=)
c.1287G>A (p.Glu429=)
c.1209G>A (p.Glu403=)
dbSNP
3g.24122891T>ACA351886451THRBc.1379A>T (p.Glu460Val)
c.*2008A>T (n.*2008A>T)
c.1424A>T (p.Glu475Val)
c.1286A>T (p.Glu429Val)
c.1208A>T (p.Glu403Val)
3g.24122891T>CCA351886450THRBc.1379A>G (p.Glu460Gly)
c.*2008A>G (n.*2008A>G)
c.1424A>G (p.Glu475Gly)
c.1286A>G (p.Glu429Gly)
c.1208A>G (p.Glu403Gly)
3g.24122891T>GCA351886449THRBc.1379A>C (p.Glu460Ala)
c.*2008A>C (n.*2008A>C)
c.1424A>C (p.Glu475Ala)
c.1286A>C (p.Glu429Ala)
c.1208A>C (p.Glu403Ala)
3g.24122892C>ACA351886452THRBc.1378G>T (p.Glu460Ter)
c.*2007G>T (n.*2007G>T)
c.1423G>T (p.Glu475Ter)
c.1285G>T (p.Glu429Ter)
c.1207G>T (p.Glu403Ter)
3g.24122892C=CA1351822108THRBc.1378G= (p.Glu460=)
c.*2007G= (n.*2007G=)
c.1423G= (p.Glu475=)
c.1285G= (p.Glu429=)
c.1207G= (p.Glu403=)
3g.24122892C>GCA351886453THRBc.1378G>C (p.Glu460Gln)
c.*2007G>C (n.*2007G>C)
c.1423G>C (p.Glu475Gln)
c.1285G>C (p.Glu429Gln)
c.1207G>C (p.Glu403Gln)
3g.24122892C>TCA351886454THRBc.1378G>A (p.Glu460Lys)
c.*2007G>A (n.*2007G>A)
c.1423G>A (p.Glu475Lys)
c.1285G>A (p.Glu429Lys)
c.1207G>A (p.Glu403Lys)
ClinVar dbSNP gnomAD v4
3g.24122893G>ACA432903888THRBc.1377C>T (p.Phe459=)
c.*2006C>T (n.*2006C>T)
c.1422C>T (p.Phe474=)
c.1284C>T (p.Phe428=)
c.1206C>T (p.Phe402=)
dbSNP gnomAD v3 gnomAD v4 COSMIC
3g.24122893G>CCA351886455THRBc.1377C>G (p.Phe459Leu)
c.*2006C>G (n.*2006C>G)
c.1422C>G (p.Phe474Leu)
c.1284C>G (p.Phe428Leu)
c.1206C>G (p.Phe402Leu)
3g.24122893G=CA1351822109THRBc.1377C= (p.Phe459=)
c.*2006C= (n.*2006C=)
c.1422C= (p.Phe474=)
c.1284C= (p.Phe428=)
c.1206C= (p.Phe402=)
3g.24122893G>TCA351886456THRBc.1377C>A (p.Phe459Leu)
c.*2006C>A (n.*2006C>A)
c.1422C>A (p.Phe474Leu)
c.1284C>A (p.Phe428Leu)
c.1206C>A (p.Phe402Leu)
ClinVar dbSNP

Number of alleles fetched