| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.115033407T>A | CA341754679 | TSHB | c.45T>A (p.Cys15Ter) | gnomAD v4 |
| 1 | g.115033407T>C | CA1022518 | TSHB | c.45T>C (p.Cys15=) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 1 | g.115033407T>G | CA341754682 | TSHB | c.45T>G (p.Cys15Trp) | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.115033407T= | CA1190425195 | TSHB | c.45T= (p.Cys15=) | |
| 1 | g.115033408G>A | CA341754684 | TSHB | c.46G>A (p.Gly16Arg) | gnomAD v4 |
| 1 | g.115033408G>C | CA341754690 | TSHB | c.46G>C (p.Gly16Arg) | dbSNP gnomAD v4 |
| 1 | g.115033408G= | CA1190425196 | TSHB | c.46G= (p.Gly16=) | |
| 1 | g.115033408G>T | CA341754692 | TSHB | c.46G>T (p.Gly16Trp) | |
| 1 | g.115033409G>A | CA29083450 | TSHB | c.47G>A (p.Gly16Glu) | dbSNP gnomAD v4 |
| 1 | g.115033409G>C | CA341754695 | TSHB | c.47G>C (p.Gly16Ala) | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.115033409G= | CA1190425197 | TSHB | c.47G= (p.Gly16=) | |
| 1 | g.115033409G>T | CA341754697 | TSHB | c.47G>T (p.Gly16Val) | |
| 1 | g.115033410G>A | CA419891299 | TSHB | c.48G>A (p.Gly16=) | |
| 1 | g.115033410G>C | CA419891298 | TSHB | c.48G>C (p.Gly16=) | |
| 1 | g.115033410G>T | CA419891297 | TSHB | c.48G>T (p.Gly16=) | dbSNP |
| 1 | g.115033411C>A | CA341754699 | TSHB | c.49C>A (p.Gln17Lys) | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.115033411C= | CA1190425198 | TSHB | c.49C= (p.Gln17=) | |
| 1 | g.115033411C>G | CA341754701 | TSHB | c.49C>G (p.Gln17Glu) | |
| 1 | g.115033411C>T | CA341754704 | TSHB | c.49C>T (p.Gln17Ter) | |
| 1 | g.115033412A>C | CA341754710 | TSHB | c.50A>C (p.Gln17Pro) | |
| 1 | g.115033412A>G | CA341754708 | TSHB | c.50A>G (p.Gln17Arg) | gnomAD v4 |
| 1 | g.115033412A>T | CA341754706 | TSHB | c.50A>T (p.Gln17Leu) | |
| 1 | g.115033413A>C | CA341754712 | TSHB | c.51A>C (p.Gln17His) | |
| 1 | g.115033413A>G | CA419891300 | TSHB | c.51A>G (p.Gln17=) | |
| 1 | g.115033413A>T | CA341754714 | TSHB | c.51A>T (p.Gln17His) | |
| 1 | g.115033414G>A | CA341754717 | TSHB | c.52G>A (p.Ala18Thr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.115033414G>C | CA341754718 | TSHB | c.52G>C (p.Ala18Pro) | |
| 1 | g.115033414G= | CA1190425199 | TSHB | c.52G= (p.Ala18=) | |
| 1 | g.115033414G>T | CA341754721 | TSHB | c.52G>T (p.Ala18Ser) | |
| 1 | g.115033415C>A | CA341754724 | TSHB | c.53C>A (p.Ala18Glu) | |
| 1 | g.115033415C= | CA1190425200 | TSHB | c.53C= (p.Ala18=) | |
| 1 | g.115033415C>G | CA341754726 | TSHB | c.53C>G (p.Ala18Gly) | |
| 1 | g.115033415C>T | CA1022519 | TSHB | c.53C>T (p.Ala18Val) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 1 | g.115033416G>A | CA1022520 | TSHB | c.54G>A (p.Ala18=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.115033416G>C | CA419891301 | TSHB | c.54G>C (p.Ala18=) | |
| 1 | g.115033416G= | CA1143007628 | TSHB | c.54G= (p.Ala18=) | |
| 1 | g.115033416G>T | CA419891302 | TSHB | c.54G>T (p.Ala18=) | |
| 1 | g.115033417A>C | CA341754732 | TSHB | c.55A>C (p.Met19Leu) | |
| 1 | g.115033417A>G | CA341754734 | TSHB | c.55A>G (p.Met19Val) | gnomAD v4 |
| 1 | g.115033417A>T | CA341754736 | TSHB | c.55A>T (p.Met19Leu) | COSMIC |
| 1 | g.115033418T>A | CA341754739 | TSHB | c.56T>A (p.Met19Lys) | |
| 1 | g.115033418T>C | CA341754743 | TSHB | c.56T>C (p.Met19Thr) | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.115033418T>G | CA341754741 | TSHB | c.56T>G (p.Met19Arg) | |
| 1 | g.115033418T= | CA1190425201 | TSHB | c.56T= (p.Met19=) | |
| 1 | g.115033419G>A | CA341754745 | TSHB | c.57G>A (p.Met19Ile) | dbSNP gnomAD v4 |
| 1 | g.115033419G>C | CA341754751 | TSHB | c.57G>C (p.Met19Ile) | |
| 1 | g.115033419G= | CA1190425202 | TSHB | c.57G= (p.Met19=) | |
| 1 | g.115033419G>T | CA341754748 | TSHB | c.57G>T (p.Met19Ile) | |
| 1 | g.115033420T>A | CA341754754 | TSHB | c.58T>A (p.Ser20Thr) | |
| 1 | g.115033420T>C | CA341754757 | TSHB | c.58T>C (p.Ser20Pro) |