| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.39665765C>A | CA399303807 | TCAP | c.160C>A (p.Gln54Lys) | gnomAD v4 |
| 17 | g.39665765C>G | CA399303806 | TCAP | c.160C>G (p.Gln54Glu) | |
| 17 | g.39665765C>T | CA399303804 | TCAP | c.160C>T (p.Gln54Ter) | |
| 17 | g.39665766A= | CA2259200647 | TCAP | c.161A= (p.Gln54=) | |
| 17 | g.39665766A>C | CA399303808 | TCAP | c.161A>C (p.Gln54Pro) | |
| 17 | g.39665766A>G | CA399303809 | TCAP | c.161A>G (p.Gln54Arg) | |
| 17 | g.39665766A>T | CA399303810 | TCAP | c.161A>T (p.Gln54Leu) | |
| 17 | g.39665767G>A | CA499889084 | TCAP | c.162G>A (p.Gln54=) | gnomAD v4 |
| 17 | g.39665767G>C | CA399303813 | TCAP | c.162G>C (p.Gln54His) | |
| 17 | g.39665767G>T | CA399303818 | TCAP | c.162G>T (p.Gln54His) | |
| 17 | g.39665770dup | CA2259200650 | TCAP | c.165dup (p.Gln56AlafsTer?) c.165dup (p.Gln56AlafsTer28) | dbSNP |
| 17 | g.39665769_39665786dup | CA626209139 | TCAP | c.164_181dup (p.Leu60_Val61insGlyGlnCysGlnValLeu) c.164_174+7dup | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.39665768G>A | CA399303820 | TCAP | c.163G>A (p.Gly55Arg) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.39665768G>C | CA399303822 | TCAP | c.163G>C (p.Gly55Arg) | gnomAD v4 |
| 17 | g.39665768G= | CA2259200653 | TCAP | c.163G= (p.Gly55=) | |
| 17 | g.39665768G>T | CA399303832 | TCAP | c.163G>T (p.Gly55Trp) | |
| 17 | g.39665769G>A | CA399303835 | TCAP | c.164G>A (p.Gly55Glu) | |
| 17 | g.39665769G>C | CA399303837 | TCAP | c.164G>C (p.Gly55Ala) | |
| 17 | g.39665769G>T | CA399303839 | TCAP | c.164G>T (p.Gly55Val) | gnomAD v4 |
| 17 | g.39665770G>A | CA290433989 | TCAP | c.165G>A (p.Gly55=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.39665770G>C | CA499889085 | TCAP | c.165G>C (p.Gly55=) | ClinVar dbSNP gnomAD v4 |
| 17 | g.39665770G= | CA2259200654 | TCAP | c.165G= (p.Gly55=) | |
| 17 | g.39665770G>T | CA499889086 | TCAP | c.165G>T (p.Gly55=) | |
| 17 | g.39665771C>A | CA399303852 | TCAP | c.166C>A (p.Gln56Lys) | |
| 17 | g.39665771C= | CA2259200657 | TCAP | c.166C= (p.Gln56=) | |
| 17 | g.39665771C>G | CA399303850 | TCAP | c.166C>G (p.Gln56Glu) | |
| 17 | g.39665771C>T | CA399303846 | TCAP | c.166C>T (p.Gln56Ter) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.39665772A>C | CA399303854 | TCAP | c.167A>C (p.Gln56Pro) | gnomAD v4 |
| 17 | g.39665772A>G | CA399303856 | TCAP | c.167A>G (p.Gln56Arg) | gnomAD v4 |
| 17 | g.39665772A>T | CA399303858 | TCAP | c.167A>T (p.Gln56Leu) | |
| 17 | g.39665773G>A | CA16615340 | TCAP | c.168G>A (p.Gln56=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.39665773G>C | CA399303860 | TCAP | c.168G>C (p.Gln56His) | |
| 17 | g.39665773G= | CA2259200660 | TCAP | c.168G= (p.Gln56=) | |
| 17 | g.39665773G>T | CA399303864 | TCAP | c.168G>T (p.Gln56His) | |
| 17 | g.39665774T>A | CA399303867 | TCAP | c.169T>A (p.Cys57Ser) | |
| 17 | g.39665774T>C | CA10604666 | TCAP | c.169T>C (p.Cys57Arg) | ClinVar dbSNP gnomAD v4 |
| 17 | g.39665774T>G | CA399303870 | TCAP | c.169T>G (p.Cys57Gly) | |
| 17 | g.39665774T= | CA2259200667 | TCAP | c.169T= (p.Cys57=) | |
| 17 | g.39665775G>A | CA8532868 | TCAP | c.170G>A (p.Cys57Tyr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.39665775G>C | CA399303875 | TCAP | c.170G>C (p.Cys57Ser) | |
| 17 | g.39665775G= | CA2259200678 | TCAP | c.170G= (p.Cys57=) | |
| 17 | g.39665775G>T | CA399303878 | TCAP | c.170G>T (p.Cys57Phe) | |
| 17 | g.39665776C>A | CA290433996 | TCAP | c.171C>A (p.Cys57Ter) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.39665776C= | CA2259200683 | TCAP | c.171C= (p.Cys57=) | |
| 17 | g.39665776C>G | CA8532869 | TCAP | c.171C>G (p.Cys57Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.39665776C>T | CA499889087 | TCAP | c.171C>T (p.Cys57=) | dbSNP |
| 17 | g.39665777C>A | CA399303884 | TCAP | c.172C>A (p.Gln58Lys) | gnomAD v4 |
| 17 | g.39665777C>G | CA399303887 | TCAP | c.172C>G (p.Gln58Glu) | ClinVar gnomAD v4 |
| 17 | g.39665777C>T | CA399303885 | TCAP | c.172C>T (p.Gln58Ter) | |
| 17 | g.39665778A= | CA2259200687 | TCAP | c.173A= (p.Gln58=) |