Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.24122935T>A | CA351886544 | THRB | c.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 |
3 | g.24122935T>C | CA432904143 | THRB | c.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 |
3 | g.24122935T>G | CA351886545 | THRB | c.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) | |
3 | g.24122935T= | CA1351822165 | THRB | c.1335A= (p.Glu445=) c.*1964A= (n.*1964A=) c.1380A= (p.Glu460=) c.1242A= (p.Glu414=) c.1164A= (p.Glu388=) | |
3 | g.24122936T>A | CA351886546 | THRB | c.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) | |
3 | g.24122936T>C | CA351886548 | THRB | c.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) | |
3 | g.24122936T>G | CA351886547 | THRB | c.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) | |
3 | g.24122937C>A | CA351886549 | THRB | c.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) | |
3 | g.24122937C>G | CA351886550 | THRB | c.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) | |
3 | g.24122937C>T | CA351886551 | THRB | c.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) | |
3 | g.24122938C>A | CA432904163 | THRB | c.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=) | |
3 | g.24122938C>G | CA432904165 | THRB | c.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=) | |
3 | g.24122938C>T | CA432904167 | THRB | c.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=) | |
3 | g.24122939A>C | CA351886552 | THRB | c.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) | |
3 | g.24122939A>G | CA351886553 | THRB | c.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) | |
3 | g.24122939A>T | CA351886554 | THRB | c.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) | |
3 | g.24122940C>A | CA351886555 | THRB | c.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) | |
3 | g.24122940C>G | CA351886556 | THRB | c.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) | |
3 | g.24122940C>T | CA351886557 | THRB | c.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) | |
3 | g.24122941C>A | CA351886558 | THRB | c.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) | |
3 | g.24122941C>G | CA351886559 | THRB | c.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) | |
3 | g.24122941C>T | CA432904182 | THRB | c.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=) | |
3 | g.24122942T>A | CA351886560 | THRB | c.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) | |
3 | g.24122942T>C | CA351886562 | THRB | c.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 |
3 | g.24122942T>G | CA351886561 | THRB | c.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) | |
3 | g.24122942T= | CA1351822167 | THRB | c.1328A= (p.Lys443=) c.*1957A= (n.*1957A=) c.1373A= (p.Lys458=) c.1235A= (p.Lys412=) c.1157A= (p.Lys386=) | |
3 | g.24122943T>A | CA351886563 | THRB | c.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) | |
3 | g.24122943T>C | CA122483 | THRB | c.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 |
3 | g.24122943T>G | CA351886564 | THRB | c.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) | |
3 | g.24122943T= | CA1351822177 | THRB | c.1327A= (p.Lys443=) c.*1956A= (n.*1956A=) c.1372A= (p.Lys458=) c.1234A= (p.Lys412=) c.1156A= (p.Lys386=) | |
3 | g.24122943_24122944delinsAT | CA658821264 | THRB | c.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 |
3 | g.24122943_24122944delinsTC | CA1351822170 | THRB | c.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=) | |
3 | g.24122944C>A | CA351886565 | THRB | c.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) | |
3 | g.24122944C>G | CA351886566 | THRB | c.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) | |
3 | g.24122944C>T | CA351886567 | THRB | c.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 |
3 | g.24122945A>C | CA351886568 | THRB | c.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) | |
3 | g.24122945A>G | CA351886569 | THRB | c.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) | |
3 | g.24122945A>T | CA351886570 | THRB | c.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) | |
3 | g.24122946T>A | CA351886571 | THRB | c.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) | |
3 | g.24122946T>C | CA122477 | THRB | c.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 |
3 | g.24122946T>G | CA351886572 | THRB | c.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) | |
3 | g.24122946T= | CA1351822182 | THRB | c.1324A= (p.Met442=) c.*1953A= (n.*1953A=) c.1369A= (p.Met457=) c.1231A= (p.Met411=) c.1153A= (p.Met385=) | |
3 | g.24122947G>A | CA432904212 | THRB | c.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 |
3 | g.24122947G>C | CA351886574 | THRB | c.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) | |
3 | g.24122947G= | CA1351822186 | THRB | c.1323C= (p.His441=) c.*1952C= (n.*1952C=) c.1368C= (p.His456=) c.1230C= (p.His410=) c.1152C= (p.His384=) | |
3 | g.24122947G>T | CA351886573 | THRB | c.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) | |
3 | g.24122948T>A | CA351886575 | THRB | c.1322A>T (p.His441Leu) c.*1951A>T (n.*1951A>T) c.1367A>T (p.His456Leu) c.1229A>T (p.His410Leu) c.1151A>T (p.His384Leu) | |
3 | g.24122948T>C | CA351886576 | THRB | c.1322A>G (p.His441Arg) c.*1951A>G (n.*1951A>G) c.1367A>G (p.His456Arg) c.1229A>G (p.His410Arg) c.1151A>G (p.His384Arg) | |
3 | g.24122948T>G | CA351886577 | THRB | c.1322A>C (p.His441Pro) c.*1951A>C (n.*1951A>C) c.1367A>C (p.His456Pro) c.1229A>C (p.His410Pro) c.1151A>C (p.His384Pro) | |
3 | g.24122949G>A | CA351886578 | THRB | c.1321C>T (p.His441Tyr) c.*1950C>T (n.*1950C>T) c.1366C>T (p.His456Tyr) c.1228C>T (p.His410Tyr) c.1150C>T (p.His384Tyr) |