| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.115033456G>A | CA1022529 | TSHB | c.94G>A (p.Glu32Lys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 1 | g.115033456G>C | CA341755032 | TSHB | c.94G>C (p.Glu32Gln) | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.115033456G= | CA1141580985 | TSHB | c.94G= (p.Glu32=) | |
| 1 | g.115033456G>T | CA122629 | TSHB | c.94G>T (p.Glu32Ter) | ClinVar dbSNP |
| 1 | g.115033457A= | CA1190425215 | TSHB | c.95A= (p.Glu32=) | |
| 1 | g.115033457A>C | CA341755036 | TSHB | c.95A>C (p.Glu32Ala) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.115033457A>G | CA29083511 | TSHB | c.95A>G (p.Glu32Gly) | dbSNP gnomAD v4 |
| 1 | g.115033457A>T | CA341755041 | TSHB | c.95A>T (p.Glu32Val) | |
| 1 | g.115033458A>C | CA341755044 | TSHB | c.96A>C (p.Glu32Asp) | |
| 1 | g.115033458A>G | CA419891346 | TSHB | c.96A>G (p.Glu32=) | |
| 1 | g.115033458A>T | CA341755047 | TSHB | c.96A>T (p.Glu32Asp) | |
| 1 | g.115033459A>C | CA419891347 | TSHB | c.97A>C (p.Arg33=) | |
| 1 | g.115033459A>G | CA341755052 | TSHB | c.97A>G (p.Arg33Gly) | |
| 1 | g.115033459A>T | CA341755054 | TSHB | c.97A>T (p.Arg33Trp) | |
| 1 | g.115033460G>A | CA341755059 | TSHB | c.98G>A (p.Arg33Lys) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 1 | g.115033460G>C | CA341755062 | TSHB | c.98G>C (p.Arg33Thr) | |
| 1 | g.115033460G= | CA1190425217 | TSHB | c.98G= (p.Arg33=) | |
| 1 | g.115033460G>T | CA341755064 | TSHB | c.98G>T (p.Arg33Met) | COSMIC |
| 1 | g.115033460_115033462delinsGGA | CA1190425216 | TSHB | c.98_100delinsGGA (p.Arg33=) | |
| 1 | g.115033461G>A | CA419891351 | TSHB | c.99G>A (p.Arg33=) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 1 | g.115033461G>C | CA341755068 | TSHB | c.99G>C (p.Arg33Ser) | COSMIC |
| 1 | g.115033461G= | CA1190425218 | TSHB | c.99G= (p.Arg33=) | |
| 1 | g.115033461G>T | CA341755071 | TSHB | c.99G>T (p.Arg33Ser) | |
| 1 | g.115033466_115033467del | CA913047927 | TSHB | c.104_105del (p.Glu35ValfsTer?) | dbSNP gnomAD v4 |
| 1 | g.115033462A>C | CA419891357 | TSHB | c.100A>C (p.Arg34=) | |
| 1 | g.115033462A>G | CA341755079 | TSHB | c.100A>G (p.Arg34Gly) | |
| 1 | g.115033462A>T | CA341755076 | TSHB | c.100A>T (p.Arg34Ter) | |
| 1 | g.115033463G>A | CA341755082 | TSHB | c.101G>A (p.Arg34Lys) | gnomAD v4 |
| 1 | g.115033463G>C | CA341755086 | TSHB | c.101G>C (p.Arg34Thr) | |
| 1 | g.115033463G= | CA1190425219 | TSHB | c.101G= (p.Arg34=) | |
| 1 | g.115033463G>T | CA341755089 | TSHB | c.101G>T (p.Arg34Ile) | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.115033464A>C | CA341755092 | TSHB | c.102A>C (p.Arg34Ser) | |
| 1 | g.115033464A>G | CA419891362 | TSHB | c.102A>G (p.Arg34=) | |
| 1 | g.115033464A>T | CA341755094 | TSHB | c.102A>T (p.Arg34Ser) | |
| 1 | g.115033465G>A | CA341755097 | TSHB | c.103G>A (p.Glu35Lys) | gnomAD v4 |
| 1 | g.115033465G>C | CA341755100 | TSHB | c.103G>C (p.Glu35Gln) | |
| 1 | g.115033465G>T | CA341755105 | TSHB | c.103G>T (p.Glu35Ter) | |
| 1 | g.115033466A>C | CA341755108 | TSHB | c.104A>C (p.Glu35Ala) | |
| 1 | g.115033466A>G | CA341755110 | TSHB | c.104A>G (p.Glu35Gly) | |
| 1 | g.115033466A>T | CA341755113 | TSHB | c.104A>T (p.Glu35Val) | |
| 1 | g.115033467G>A | CA419891369 | TSHB | c.105G>A (p.Glu35=) | |
| 1 | g.115033467G>C | CA341755116 | TSHB | c.105G>C (p.Glu35Asp) | |
| 1 | g.115033467G>T | CA341755119 | TSHB | c.105G>T (p.Glu35Asp) | |
| 1 | g.115033470_115033471del | CA2580611475 | TSHB | c.108_109del (p.Ala37LeufsTer?) | ClinVar dbSNP gnomAD v4 |
| 1 | g.115033468T>A | CA341755127 | TSHB | c.106T>A (p.Cys36Ser) | |
| 1 | g.115033468T>C | CA341755131 | TSHB | c.106T>C (p.Cys36Arg) | |
| 1 | g.115033468T>G | CA341755124 | TSHB | c.106T>G (p.Cys36Gly) | |
| 1 | g.115033469G>A | CA341755141 | TSHB | c.107G>A (p.Cys36Tyr) | COSMIC |
| 1 | g.115033469G>C | CA341755136 | TSHB | c.107G>C (p.Cys36Ser) | |
| 1 | g.115033469G>T | CA341755139 | TSHB | c.107G>T (p.Cys36Phe) |