Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.115033466_115033467del | CA913047927 | TSHB | c.104_105del (p.Glu35ValfsTer?) | dbSNP gnomAD v4 |
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) | |
1 | g.115033470T>A | CA341755144 | TSHB | c.108T>A (p.Cys36Ter) | |
1 | g.115033470T>C | CA419891374 | TSHB | c.108T>C (p.Cys36=) | |
1 | g.115033470T>G | CA341755147 | TSHB | c.108T>G (p.Cys36Trp) | |
1 | g.115033471G>A | CA341755152 | TSHB | c.109G>A (p.Ala37Thr) | |
1 | g.115033471G>C | CA341755155 | TSHB | c.109G>C (p.Ala37Pro) | |
1 | g.115033471G>T | CA341755158 | TSHB | c.109G>T (p.Ala37Ser) | |
1 | g.115033472C>A | CA341755164 | TSHB | c.110C>A (p.Ala37Asp) | |
1 | g.115033472C>G | CA341755166 | TSHB | c.110C>G (p.Ala37Gly) | |
1 | g.115033472C>T | CA341755168 | TSHB | c.110C>T (p.Ala37Val) | |
1 | g.115033473T>A | CA419891379 | TSHB | c.111T>A (p.Ala37=) | |
1 | g.115033473T>C | CA419891380 | TSHB | c.111T>C (p.Ala37=) | COSMIC |
1 | g.115033473T>G | CA419891381 | TSHB | c.111T>G (p.Ala37=) | |
1 | g.115033474T>A | CA341755171 | TSHB | c.112T>A (p.Tyr38Asn) | |
1 | g.115033474T>C | CA341755174 | TSHB | c.112T>C (p.Tyr38His) | |
1 | g.115033474T>G | CA341755177 | TSHB | c.112T>G (p.Tyr38Asp) | |
1 | g.115033475A= | CA1190425220 | TSHB | c.113A= (p.Tyr38=) | |
1 | g.115033475A>C | CA341755185 | TSHB | c.113A>C (p.Tyr38Ser) | |
1 | g.115033475A>G | CA341755181 | TSHB | c.113A>G (p.Tyr38Cys) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
1 | g.115033475A>T | CA341755184 | TSHB | c.113A>T (p.Tyr38Phe) | |
1 | g.115033476T>A | CA341755189 | TSHB | c.114T>A (p.Tyr38Ter) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.115033476T>C | CA419891387 | TSHB | c.114T>C (p.Tyr38=) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.115033476T>G | CA341755191 | TSHB | c.114T>G (p.Tyr38Ter) | |
1 | g.115033476T= | CA1190425221 | TSHB | c.114T= (p.Tyr38=) | |
1 | g.115033477T>A | CA341755195 | TSHB | c.115T>A (p.Cys39Ser) | |
1 | g.115033477T>C | CA341755196 | TSHB | c.115T>C (p.Cys39Arg) | |
1 | g.115033477T>G | CA341755199 | TSHB | c.115T>G (p.Cys39Gly) | |
1 | g.115033478G>A | CA341755202 | TSHB | c.116G>A (p.Cys39Tyr) | |
1 | g.115033478G>C | CA341755203 | TSHB | c.116G>C (p.Cys39Ser) | |
1 | g.115033478G>T | CA341755205 | TSHB | c.116G>T (p.Cys39Phe) | |
1 | g.115033479C>A | CA341755208 | TSHB | c.117C>A (p.Cys39Ter) | |
1 | g.115033479C>G | CA341755211 | TSHB | c.117C>G (p.Cys39Trp) | |
1 | g.115033479C>T | CA419891394 | TSHB | c.117C>T (p.Cys39=) | gnomAD v4 |
1 | g.115033480C>A | CA341755214 | TSHB | c.118C>A (p.Leu40Ile) | |
1 | g.115033480C= | CA1190425222 | TSHB | c.118C= (p.Leu40=) | |
1 | g.115033480C>G | CA341755216 | TSHB | c.118C>G (p.Leu40Val) | gnomAD v4 |
1 | g.115033480C>T | CA419891396 | TSHB | c.118C>T (p.Leu40=) | dbSNP |
1 | g.115033481T>A | CA29083516 | TSHB | c.119T>A (p.Leu40Gln) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.115033481T>C | CA341755223 | TSHB | c.119T>C (p.Leu40Pro) | |
1 | g.115033481T>G | CA341755220 | TSHB | c.119T>G (p.Leu40Arg) |