Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.115033372C>A | CA341754519 | TSHB | c.10C>A (p.Leu4Ile) | |
1 | g.115033372C= | CA1190425185 | TSHB | c.10C= (p.Leu4=) | |
1 | g.115033372C>G | CA341754514 | TSHB | c.10C>G (p.Leu4Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.115033372C>T | CA1022514 | TSHB | c.10C>T (p.Leu4Phe) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.115033373T>A | CA341754524 | TSHB | c.11T>A (p.Leu4His) | |
1 | g.115033373T>C | CA341754528 | TSHB | c.11T>C (p.Leu4Pro) | |
1 | g.115033373T>G | CA341754531 | TSHB | c.11T>G (p.Leu4Arg) | |
1 | g.115033374C>A | CA419891272 | TSHB | c.12C>A (p.Leu4=) | |
1 | g.115033374C>G | CA419891273 | TSHB | c.12C>G (p.Leu4=) | |
1 | g.115033374C>T | CA419891274 | TSHB | c.12C>T (p.Leu4=) | ClinVar |
1 | g.115033375T>A | CA341754537 | TSHB | c.13T>A (p.Phe5Ile) | |
1 | g.115033375T>C | CA341754539 | TSHB | c.13T>C (p.Phe5Leu) | dbSNP gnomAD v4 |
1 | g.115033375T>G | CA341754543 | TSHB | c.13T>G (p.Phe5Val) | |
1 | g.115033375T= | CA1190425186 | TSHB | c.13T= (p.Phe5=) | |
1 | g.115033376T>A | CA341754545 | TSHB | c.14T>A (p.Phe5Tyr) | |
1 | g.115033376T>C | CA341754547 | TSHB | c.14T>C (p.Phe5Ser) | gnomAD v4 |
1 | g.115033376T>G | CA341754549 | TSHB | c.14T>G (p.Phe5Cys) | |
1 | g.115033377T>A | CA341754553 | TSHB | c.15T>A (p.Phe5Leu) | |
1 | g.115033377T>C | CA419891276 | TSHB | c.15T>C (p.Phe5=) | |
1 | g.115033377T>G | CA341754554 | TSHB | c.15T>G (p.Phe5Leu) | |
1 | g.115033379_115033385del | CA2647270341 | TSHB | c.17_23del (p.Leu6ProfsTer?) | gnomAD v4 |
1 | g.115033378C>A | CA341754556 | TSHB | c.16C>A (p.Leu6Met) | gnomAD v4 |
1 | g.115033378C>G | CA341754561 | TSHB | c.16C>G (p.Leu6Val) | |
1 | g.115033378C>T | CA419891277 | TSHB | c.16C>T (p.Leu6=) | |
1 | g.115033379T>A | CA341754565 | TSHB | c.17T>A (p.Leu6Gln) | |
1 | g.115033379T>C | CA341754567 | TSHB | c.17T>C (p.Leu6Pro) | |
1 | g.115033379T>G | CA341754569 | TSHB | c.17T>G (p.Leu6Arg) | |
1 | g.115033380G>A | CA419891278 | TSHB | c.18G>A (p.Leu6=) | |
1 | g.115033380G>C | CA419891279 | TSHB | c.18G>C (p.Leu6=) | |
1 | g.115033380G>T | CA419891280 | TSHB | c.18G>T (p.Leu6=) | |
1 | g.115033381A>C | CA341754572 | TSHB | c.19A>C (p.Met7Leu) | |
1 | g.115033381A>G | CA341754573 | TSHB | c.19A>G (p.Met7Val) | |
1 | g.115033381A>T | CA341754576 | TSHB | c.19A>T (p.Met7Leu) | |
1 | g.115033382del | CA2647270342 | TSHB | c.20del (p.Met7SerfsTer?) | gnomAD v4 |
1 | g.115033382T>A | CA341754578 | TSHB | c.20T>A (p.Met7Lys) | |
1 | g.115033382T>C | CA341754579 | TSHB | c.20T>C (p.Met7Thr) | dbSNP |
1 | g.115033382T>G | CA341754580 | TSHB | c.20T>G (p.Met7Arg) | |
1 | g.115033382T= | CA1190425187 | TSHB | c.20T= (p.Met7=) | |
1 | g.115033383G>A | CA341754581 | TSHB | c.21G>A (p.Met7Ile) | dbSNP |
1 | g.115033383G>C | CA341754582 | TSHB | c.21G>C (p.Met7Ile) | |
1 | g.115033383G= | CA1190425188 | TSHB | c.21G= (p.Met7=) | |
1 | g.115033383G>T | CA341754583 | TSHB | c.21G>T (p.Met7Ile) | |
1 | g.115033384T>A | CA341754590 | TSHB | c.22T>A (p.Ser8Thr) | |
1 | g.115033384T>C | CA341754586 | TSHB | c.22T>C (p.Ser8Pro) | |
1 | g.115033384T>G | CA341754588 | TSHB | c.22T>G (p.Ser8Ala) | |
1 | g.115033384_115033386del | CA2647270343 | TSHB | c.22_24del (p.Ser8del) | gnomAD v4 |
1 | g.115033385C>A | CA341754592 | TSHB | c.23C>A (p.Ser8Tyr) | |
1 | g.115033385C>G | CA341754593 | TSHB | c.23C>G (p.Ser8Cys) | |
1 | g.115033385C>T | CA341754594 | TSHB | c.23C>T (p.Ser8Phe) | COSMIC |
1 | g.115033386C>A | CA419891281 | TSHB | c.24C>A (p.Ser8=) |