Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.24122934A=CA1351822161THRBc.1336T= (p.Cys446=)
c.*1965T= (n.*1965T=)
c.1381T= (p.Cys461=)
c.1243T= (p.Cys415=)
c.1165T= (p.Cys389=)
3g.24122934A>CCA351886542THRBc.1336T>G (p.Cys446Gly)
c.*1965T>G (n.*1965T>G)
c.1381T>G (p.Cys461Gly)
c.1243T>G (p.Cys415Gly)
c.1165T>G (p.Cys389Gly)
ClinVar
3g.24122934A>GCA122503THRBc.1336T>C (p.Cys446Arg)
c.*1965T>C (n.*1965T>C)
c.1381T>C (p.Cys461Arg)
c.1243T>C (p.Cys415Arg)
c.1165T>C (p.Cys389Arg)
ClinVar dbSNP
3g.24122934A>TCA351886543THRBc.1336T>A (p.Cys446Ser)
c.*1965T>A (n.*1965T>A)
c.1381T>A (p.Cys461Ser)
c.1243T>A (p.Cys415Ser)
c.1165T>A (p.Cys389Ser)
3g.24122935T>ACA351886544THRBc.1335A>T (p.Glu445Asp)
c.*1964A>T (n.*1964A>T)
c.1380A>T (p.Glu460Asp)
c.1242A>T (p.Glu414Asp)
c.1164A>T (p.Glu388Asp)
ClinVar dbSNP
3g.24122935T>CCA432904143THRBc.1335A>G (p.Glu445=)
c.*1964A>G (n.*1964A>G)
c.1380A>G (p.Glu460=)
c.1242A>G (p.Glu414=)
c.1164A>G (p.Glu388=)
dbSNP
3g.24122935T>GCA351886545THRBc.1335A>C (p.Glu445Asp)
c.*1964A>C (n.*1964A>C)
c.1380A>C (p.Glu460Asp)
c.1242A>C (p.Glu414Asp)
c.1164A>C (p.Glu388Asp)
3g.24122935T=CA1351822165THRBc.1335A= (p.Glu445=)
c.*1964A= (n.*1964A=)
c.1380A= (p.Glu460=)
c.1242A= (p.Glu414=)
c.1164A= (p.Glu388=)
3g.24122936T>ACA351886546THRBc.1334A>T (p.Glu445Val)
c.*1963A>T (n.*1963A>T)
c.1379A>T (p.Glu460Val)
c.1241A>T (p.Glu414Val)
c.1163A>T (p.Glu388Val)
3g.24122936T>CCA351886548THRBc.1334A>G (p.Glu445Gly)
c.*1963A>G (n.*1963A>G)
c.1379A>G (p.Glu460Gly)
c.1241A>G (p.Glu414Gly)
c.1163A>G (p.Glu388Gly)
3g.24122936T>GCA351886547THRBc.1334A>C (p.Glu445Ala)
c.*1963A>C (n.*1963A>C)
c.1379A>C (p.Glu460Ala)
c.1241A>C (p.Glu414Ala)
c.1163A>C (p.Glu388Ala)
3g.24122937C>ACA351886549THRBc.1333G>T (p.Glu445Ter)
c.*1962G>T (n.*1962G>T)
c.1378G>T (p.Glu460Ter)
c.1240G>T (p.Glu414Ter)
c.1162G>T (p.Glu388Ter)
3g.24122937C>GCA351886550THRBc.1333G>C (p.Glu445Gln)
c.*1962G>C (n.*1962G>C)
c.1378G>C (p.Glu460Gln)
c.1240G>C (p.Glu414Gln)
c.1162G>C (p.Glu388Gln)
3g.24122937C>TCA351886551THRBc.1333G>A (p.Glu445Lys)
c.*1962G>A (n.*1962G>A)
c.1378G>A (p.Glu460Lys)
c.1240G>A (p.Glu414Lys)
c.1162G>A (p.Glu388Lys)
3g.24122938C>ACA432904163THRBc.1332G>T (p.Val444=)
c.*1961G>T (n.*1961G>T)
c.1377G>T (p.Val459=)
c.1239G>T (p.Val413=)
c.1161G>T (p.Val387=)
3g.24122938C>GCA432904165THRBc.1332G>C (p.Val444=)
c.*1961G>C (n.*1961G>C)
c.1377G>C (p.Val459=)
c.1239G>C (p.Val413=)
c.1161G>C (p.Val387=)
3g.24122938C>TCA432904167THRBc.1332G>A (p.Val444=)
c.*1961G>A (n.*1961G>A)
c.1377G>A (p.Val459=)
c.1239G>A (p.Val413=)
c.1161G>A (p.Val387=)
3g.24122939A>CCA351886552THRBc.1331T>G (p.Val444Gly)
c.*1960T>G (n.*1960T>G)
c.1376T>G (p.Val459Gly)
c.1238T>G (p.Val413Gly)
c.1160T>G (p.Val387Gly)
3g.24122939A>GCA351886553THRBc.1331T>C (p.Val444Ala)
c.*1960T>C (n.*1960T>C)
c.1376T>C (p.Val459Ala)
c.1238T>C (p.Val413Ala)
c.1160T>C (p.Val387Ala)
3g.24122939A>TCA351886554THRBc.1331T>A (p.Val444Glu)
c.*1960T>A (n.*1960T>A)
c.1376T>A (p.Val459Glu)
c.1238T>A (p.Val413Glu)
c.1160T>A (p.Val387Glu)
3g.24122940C>ACA351886555THRBc.1330G>T (p.Val444Leu)
c.*1959G>T (n.*1959G>T)
c.1375G>T (p.Val459Leu)
c.1237G>T (p.Val413Leu)
c.1159G>T (p.Val387Leu)
3g.24122940C>GCA351886556THRBc.1330G>C (p.Val444Leu)
c.*1959G>C (n.*1959G>C)
c.1375G>C (p.Val459Leu)
c.1237G>C (p.Val413Leu)
c.1159G>C (p.Val387Leu)
3g.24122940C>TCA351886557THRBc.1330G>A (p.Val444Met)
c.*1959G>A (n.*1959G>A)
c.1375G>A (p.Val459Met)
c.1237G>A (p.Val413Met)
c.1159G>A (p.Val387Met)
3g.24122941C>ACA351886558THRBc.1329G>T (p.Lys443Asn)
c.*1958G>T (n.*1958G>T)
c.1374G>T (p.Lys458Asn)
c.1236G>T (p.Lys412Asn)
c.1158G>T (p.Lys386Asn)
3g.24122941C>GCA351886559THRBc.1329G>C (p.Lys443Asn)
c.*1958G>C (n.*1958G>C)
c.1374G>C (p.Lys458Asn)
c.1236G>C (p.Lys412Asn)
c.1158G>C (p.Lys386Asn)
3g.24122941C>TCA432904182THRBc.1329G>A (p.Lys443=)
c.*1958G>A (n.*1958G>A)
c.1374G>A (p.Lys458=)
c.1236G>A (p.Lys412=)
c.1158G>A (p.Lys386=)
3g.24122942T>ACA351886560THRBc.1328A>T (p.Lys443Met)
c.*1957A>T (n.*1957A>T)
c.1373A>T (p.Lys458Met)
c.1235A>T (p.Lys412Met)
c.1157A>T (p.Lys386Met)
3g.24122942T>CCA351886562THRBc.1328A>G (p.Lys443Arg)
c.*1957A>G (n.*1957A>G)
c.1373A>G (p.Lys458Arg)
c.1235A>G (p.Lys412Arg)
c.1157A>G (p.Lys386Arg)
dbSNP gnomAD v3 gnomAD v4
3g.24122942T>GCA351886561THRBc.1328A>C (p.Lys443Thr)
c.*1957A>C (n.*1957A>C)
c.1373A>C (p.Lys458Thr)
c.1235A>C (p.Lys412Thr)
c.1157A>C (p.Lys386Thr)
3g.24122942T=CA1351822167THRBc.1328A= (p.Lys443=)
c.*1957A= (n.*1957A=)
c.1373A= (p.Lys458=)
c.1235A= (p.Lys412=)
c.1157A= (p.Lys386=)
3g.24122943T>ACA351886563THRBc.1327A>T (p.Lys443Ter)
c.*1956A>T (n.*1956A>T)
c.1372A>T (p.Lys458Ter)
c.1234A>T (p.Lys412Ter)
c.1156A>T (p.Lys386Ter)
3g.24122943T>CCA122483THRBc.1327A>G (p.Lys443Glu)
c.*1956A>G (n.*1956A>G)
c.1372A>G (p.Lys458Glu)
c.1234A>G (p.Lys412Glu)
c.1156A>G (p.Lys386Glu)
ClinVar dbSNP
3g.24122943T>GCA351886564THRBc.1327A>C (p.Lys443Gln)
c.*1956A>C (n.*1956A>C)
c.1372A>C (p.Lys458Gln)
c.1234A>C (p.Lys412Gln)
c.1156A>C (p.Lys386Gln)
3g.24122943T=CA1351822177THRBc.1327A= (p.Lys443=)
c.*1956A= (n.*1956A=)
c.1372A= (p.Lys458=)
c.1234A= (p.Lys412=)
c.1156A= (p.Lys386=)
3g.24122943_24122944delinsATCA658821264THRBc.1326_1327delinsAT (p.Met442IlefsTer2)
c.*1955_*1956delinsAT (n.*1955_*1956delinsAT)
c.1371_1372delinsAT (p.Met457IlefsTer2)
c.1233_1234delinsAT (p.Met411IlefsTer2)
c.1155_1156delinsAT (p.Met385IlefsTer2)
ClinVar dbSNP
3g.24122943_24122944delinsTCCA1351822170THRBc.1326_1327delinsGA (p.Met442=)
c.*1955_*1956delinsGA (n.*1955_*1956delinsGA)
c.1371_1372delinsGA (p.Met457=)
c.1233_1234delinsGA (p.Met411=)
c.1155_1156delinsGA (p.Met385=)
3g.24122944C>ACA351886565THRBc.1326G>T (p.Met442Ile)
c.*1955G>T (n.*1955G>T)
c.1371G>T (p.Met457Ile)
c.1233G>T (p.Met411Ile)
c.1155G>T (p.Met385Ile)
3g.24122944C>GCA351886566THRBc.1326G>C (p.Met442Ile)
c.*1955G>C (n.*1955G>C)
c.1371G>C (p.Met457Ile)
c.1233G>C (p.Met411Ile)
c.1155G>C (p.Met385Ile)
3g.24122944C>TCA351886567THRBc.1326G>A (p.Met442Ile)
c.*1955G>A (n.*1955G>A)
c.1371G>A (p.Met457Ile)
c.1233G>A (p.Met411Ile)
c.1155G>A (p.Met385Ile)
COSMIC
3g.24122945A>CCA351886568THRBc.1325T>G (p.Met442Arg)
c.*1954T>G (n.*1954T>G)
c.1370T>G (p.Met457Arg)
c.1232T>G (p.Met411Arg)
c.1154T>G (p.Met385Arg)
3g.24122945A>GCA351886569THRBc.1325T>C (p.Met442Thr)
c.*1954T>C (n.*1954T>C)
c.1370T>C (p.Met457Thr)
c.1232T>C (p.Met411Thr)
c.1154T>C (p.Met385Thr)
3g.24122945A>TCA351886570THRBc.1325T>A (p.Met442Lys)
c.*1954T>A (n.*1954T>A)
c.1370T>A (p.Met457Lys)
c.1232T>A (p.Met411Lys)
c.1154T>A (p.Met385Lys)
3g.24122946T>ACA351886571THRBc.1324A>T (p.Met442Leu)
c.*1953A>T (n.*1953A>T)
c.1369A>T (p.Met457Leu)
c.1231A>T (p.Met411Leu)
c.1153A>T (p.Met385Leu)
3g.24122946T>CCA122477THRBc.1324A>G (p.Met442Val)
c.*1953A>G (n.*1953A>G)
c.1369A>G (p.Met457Val)
c.1231A>G (p.Met411Val)
c.1153A>G (p.Met385Val)
ClinVar dbSNP
3g.24122946T>GCA351886572THRBc.1324A>C (p.Met442Leu)
c.*1953A>C (n.*1953A>C)
c.1369A>C (p.Met457Leu)
c.1231A>C (p.Met411Leu)
c.1153A>C (p.Met385Leu)
3g.24122946T=CA1351822182THRBc.1324A= (p.Met442=)
c.*1953A= (n.*1953A=)
c.1369A= (p.Met457=)
c.1231A= (p.Met411=)
c.1153A= (p.Met385=)
3g.24122947G>ACA432904212THRBc.1323C>T (p.His441=)
c.*1952C>T (n.*1952C>T)
c.1368C>T (p.His456=)
c.1230C>T (p.His410=)
c.1152C>T (p.His384=)
dbSNP gnomAD v2 gnomAD v4
3g.24122947G>CCA351886574THRBc.1323C>G (p.His441Gln)
c.*1952C>G (n.*1952C>G)
c.1368C>G (p.His456Gln)
c.1230C>G (p.His410Gln)
c.1152C>G (p.His384Gln)
3g.24122947G=CA1351822186THRBc.1323C= (p.His441=)
c.*1952C= (n.*1952C=)
c.1368C= (p.His456=)
c.1230C= (p.His410=)
c.1152C= (p.His384=)
3g.24122947G>TCA351886573THRBc.1323C>A (p.His441Gln)
c.*1952C>A (n.*1952C>A)
c.1368C>A (p.His456Gln)
c.1230C>A (p.His410Gln)
c.1152C>A (p.His384Gln)

Number of alleles fetched