| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.39665858_39665881del | CA2637632742 | TCAP | c.253_276del (p.Tyr85_Pro92del) c.181_204del | gnomAD v4 |
| 17 | g.39665865G>A | CA253520 | TCAP | c.260G>A (p.Arg87Gln) c.188G>A (p.Arg63Gln) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.39665865G>C | CA399304641 | TCAP | c.260G>C (p.Arg87Pro) c.188G>C (p.Arg63Pro) | |
| 17 | g.39665865G= | CA2259200783 | TCAP | c.260G= (p.Arg87=) c.188G= (p.Arg63=) | |
| 17 | g.39665865G>T | CA399304637 | TCAP | c.260G>T (p.Arg87Leu) c.188G>T (p.Arg63Leu) | |
| 17 | g.39665866G>A | CA499889145 | TCAP | c.261G>A (p.Arg87=) c.189G>A (p.Arg63=) | |
| 17 | g.39665866G>C | CA290434072 | TCAP | c.261G>C (p.Arg87=) c.189G>C (p.Arg63=) | dbSNP |
| 17 | g.39665866G= | CA2259200784 | TCAP | c.261G= (p.Arg87=) c.189G= (p.Arg63=) | |
| 17 | g.39665866G>T | CA8532884 | TCAP | c.261G>T (p.Arg87=) c.189G>T (p.Arg63=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.39665867G>A | CA399304654 | TCAP | c.262G>A (p.Val88Ile) c.190G>A (p.Val64Ile) | gnomAD v4 |
| 17 | g.39665867G>C | CA399304649 | TCAP | c.262G>C (p.Val88Leu) c.190G>C (p.Val64Leu) | |
| 17 | g.39665867G= | CA2259200785 | TCAP | c.262G= (p.Val88=) c.190G= (p.Val64=) | |
| 17 | g.39665867G>T | CA8532885 | TCAP | c.262G>T (p.Val88Leu) c.190G>T (p.Val64Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.39665868T>A | CA399304658 | TCAP | c.263T>A (p.Val88Glu) c.191T>A (p.Val64Glu) | ClinVar |
| 17 | g.39665868T>C | CA399304661 | TCAP | c.263T>C (p.Val88Ala) c.191T>C (p.Val64Ala) | |
| 17 | g.39665868T>G | CA399304665 | TCAP | c.263T>G (p.Val88Gly) c.191T>G (p.Val64Gly) | |
| 17 | g.39665869A= | CA2259200786 | TCAP | c.264A= (p.Val88=) c.192A= (p.Val64=) | |
| 17 | g.39665869A>C | CA499889146 | TCAP | c.264A>C (p.Val88=) c.192A>C (p.Val64=) | |
| 17 | g.39665869A>G | CA499889147 | TCAP | c.264A>G (p.Val88=) c.192A>G (p.Val64=) | dbSNP |
| 17 | g.39665869A>T | CA8532886 | TCAP | c.264A>T (p.Val88=) c.192A>T (p.Val64=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.39665870C>A | CA399304673 | TCAP | c.265C>A (p.Leu89Met) c.193C>A (p.Leu65Met) | ClinVar |
| 17 | g.39665870C= | CA2259200787 | TCAP | c.265C= (p.Leu89=) c.193C= (p.Leu65=) | |
| 17 | g.39665870C>G | CA399304676 | TCAP | c.265C>G (p.Leu89Val) c.193C>G (p.Leu65Val) | |
| 17 | g.39665870C>T | CA499889148 | TCAP | c.265C>T (p.Leu89=) c.193C>T (p.Leu65=) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.39665871T>A | CA399304681 | TCAP | c.266T>A (p.Leu89Gln) c.194T>A (p.Leu65Gln) | |
| 17 | g.39665871T>C | CA399304684 | TCAP | c.266T>C (p.Leu89Pro) c.194T>C (p.Leu65Pro) | |
| 17 | g.39665871T>G | CA399304687 | TCAP | c.266T>G (p.Leu89Arg) c.194T>G (p.Leu65Arg) | |
| 17 | g.39665872G>A | CA499889149 | TCAP | c.267G>A (p.Leu89=) c.195G>A (p.Leu65=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.39665872G>C | CA499889150 | TCAP | c.267G>C (p.Leu89=) c.195G>C (p.Leu65=) | |
| 17 | g.39665872G= | CA2259200788 | TCAP | c.267G= (p.Leu89=) c.195G= (p.Leu65=) | |
| 17 | g.39665872G>T | CA499889151 | TCAP | c.267G>T (p.Leu89=) c.195G>T (p.Leu65=) | |
| 17 | g.39665873C>A | CA399304698 | TCAP | c.268C>A (p.Pro90Thr) c.196C>A (p.Pro66Thr) | |
| 17 | g.39665873C= | CA2259200789 | TCAP | c.268C= (p.Pro90=) c.196C= (p.Pro66=) | |
| 17 | g.39665873C>G | CA399304703 | TCAP | c.268C>G (p.Pro90Ala) c.196C>G (p.Pro66Ala) | dbSNP |
| 17 | g.39665873C>T | CA399304705 | TCAP | c.268C>T (p.Pro90Ser) c.196C>T (p.Pro66Ser) | dbSNP gnomAD v2 |
| 17 | g.39665874C>A | CA399304716 | TCAP | c.269C>A (p.Pro90Gln) c.197C>A (p.Pro66Gln) | ClinVar dbSNP |
| 17 | g.39665874C= | CA2259200790 | TCAP | c.269C= (p.Pro90=) c.197C= (p.Pro66=) | |
| 17 | g.39665874C>G | CA399304712 | TCAP | c.269C>G (p.Pro90Arg) c.197C>G (p.Pro66Arg) | |
| 17 | g.39665874C>T | CA181091 | TCAP | c.269C>T (p.Pro90Leu) c.197C>T (p.Pro66Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 17 | g.39665875G>A | CA241513 | TCAP | c.270G>A (p.Pro90=) c.198G>A (p.Pro66=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.39665875G>C | CA499889152 | TCAP | c.270G>C (p.Pro90=) c.198G>C (p.Pro66=) | |
| 17 | g.39665875G= | CA2259200791 | TCAP | c.270G= (p.Pro90=) c.198G= (p.Pro66=) | |
| 17 | g.39665875G>T | CA499889153 | TCAP | c.270G>T (p.Pro90=) c.198G>T (p.Pro66=) | dbSNP |
| 17 | g.39665876C>A | CA399304725 | TCAP | c.271C>A (p.Leu91Met) c.199C>A (p.Leu67Met) | ClinVar |
| 17 | g.39665876C>G | CA399304727 | TCAP | c.271C>G (p.Leu91Val) c.199C>G (p.Leu67Val) | |
| 17 | g.39665876C>T | CA499889154 | TCAP | c.271C>T (p.Leu91=) c.199C>T (p.Leu67=) | |
| 17 | g.39665877T>A | CA399304736 | TCAP | c.272T>A (p.Leu91Gln) c.200T>A (p.Leu67Gln) | |
| 17 | g.39665877T>C | CA399304739 | TCAP | c.272T>C (p.Leu91Pro) c.200T>C (p.Leu67Pro) | |
| 17 | g.39665877T>G | CA399304742 | TCAP | c.272T>G (p.Leu91Arg) c.200T>G (p.Leu67Arg) | |
| 17 | g.39665878G>A | CA499889155 | TCAP | c.273G>A (p.Leu91=) c.201G>A (p.Leu67=) | dbSNP |