| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.74754985T>A | CA393170260 | CYP1A2 | c.1448T>A (p.Val483Glu) | gnomAD v4 |
| 15 | g.74754985T>C | CA393170264 | CYP1A2 | c.1448T>C (p.Val483Ala) | |
| 15 | g.74754985T>G | CA393170265 | CYP1A2 | c.1448T>G (p.Val483Gly) | |
| 15 | g.74754986G>A | CA491489784 | CYP1A2 | c.1449G>A (p.Val483=) | |
| 15 | g.74754986G>C | CA491489782 | CYP1A2 | c.1449G>C (p.Val483=) | |
| 15 | g.74754986G>T | CA491489783 | CYP1A2 | c.1449G>T (p.Val483=) | |
| 15 | g.74754987C>A | CA393170266 | CYP1A2 | c.1450C>A (p.Pro484Thr) | COSMIC |
| 15 | g.74754987C= | CA2187827130 | CYP1A2 | c.1450C= (p.Pro484=) | |
| 15 | g.74754987C>G | CA393170267 | CYP1A2 | c.1450C>G (p.Pro484Ala) | |
| 15 | g.74754987C>T | CA393170268 | CYP1A2 | c.1450C>T (p.Pro484Ser) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.74754988C>A | CA393170272 | CYP1A2 | c.1451C>A (p.Pro484Gln) | |
| 15 | g.74754988C= | CA2187827131 | CYP1A2 | c.1451C= (p.Pro484=) | |
| 15 | g.74754988C>G | CA393170277 | CYP1A2 | c.1451C>G (p.Pro484Arg) | |
| 15 | g.74754988C>T | CA272816156 | CYP1A2 | c.1451C>T (p.Pro484Leu) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.74754989G>A | CA7660116 | CYP1A2 | c.1452G>A (p.Pro484=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.74754989G>C | CA491489785 | CYP1A2 | c.1452G>C (p.Pro484=) | |
| 15 | g.74754989G= | CA2187827132 | CYP1A2 | c.1452G= (p.Pro484=) | |
| 15 | g.74754989G>T | CA491489786 | CYP1A2 | c.1452G>T (p.Pro484=) | |
| 15 | g.74754990C>A | CA393170282 | CYP1A2 | c.1453C>A (p.Pro485Thr) | |
| 15 | g.74754990C>G | CA393170285 | CYP1A2 | c.1453C>G (p.Pro485Ala) | |
| 15 | g.74754990C>T | CA393170289 | CYP1A2 | c.1453C>T (p.Pro485Ser) | |
| 15 | g.74754991C>A | CA393170292 | CYP1A2 | c.1454C>A (p.Pro485Gln) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.74754991C= | CA2187827133 | CYP1A2 | c.1454C= (p.Pro485=) | |
| 15 | g.74754991C>G | CA393170296 | CYP1A2 | c.1454C>G (p.Pro485Arg) | gnomAD v4 |
| 15 | g.74754991C>T | CA7660117 | CYP1A2 | c.1454C>T (p.Pro485Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.74754992G>A | CA7660118 | CYP1A2 | c.1455G>A (p.Pro485=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.74754992G>C | CA491489787 | CYP1A2 | c.1455G>C (p.Pro485=) | |
| 15 | g.74754992G= | CA2187827134 | CYP1A2 | c.1455G= (p.Pro485=) | |
| 15 | g.74754992G>T | CA491489788 | CYP1A2 | c.1455G>T (p.Pro485=) | gnomAD v4 |
| 15 | g.74754993G>A | CA393170305 | CYP1A2 | c.1456G>A (p.Gly486Ser) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.74754993G>C | CA393170311 | CYP1A2 | c.1456G>C (p.Gly486Arg) | |
| 15 | g.74754993G= | CA2187827135 | CYP1A2 | c.1456G= (p.Gly486=) | |
| 15 | g.74754993G>T | CA393170315 | CYP1A2 | c.1456G>T (p.Gly486Cys) | |
| 15 | g.74754994G>A | CA7660119 | CYP1A2 | c.1457G>A (p.Gly486Asp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.74754994G>C | CA393170324 | CYP1A2 | c.1457G>C (p.Gly486Ala) | |
| 15 | g.74754994G= | CA2187827136 | CYP1A2 | c.1457G= (p.Gly486=) | |
| 15 | g.74754994G>T | CA393170319 | CYP1A2 | c.1457G>T (p.Gly486Val) | COSMIC |
| 15 | g.74754995C>A | CA7660120 | CYP1A2 | c.1458C>A (p.Gly486=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.74754995C= | CA2187827137 | CYP1A2 | c.1458C= (p.Gly486=) | |
| 15 | g.74754995C>G | CA491489789 | CYP1A2 | c.1458C>G (p.Gly486=) | |
| 15 | g.74754995C>T | CA491489790 | CYP1A2 | c.1458C>T (p.Gly486=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.74754996G>A | CA7660121 | CYP1A2 | c.1459G>A (p.Val487Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.74754996G>C | CA393170340 | CYP1A2 | c.1459G>C (p.Val487Leu) | |
| 15 | g.74754996G= | CA2187827138 | CYP1A2 | c.1459G= (p.Val487=) | |
| 15 | g.74754996G>T | CA393170342 | CYP1A2 | c.1459G>T (p.Val487Leu) | |
| 15 | g.74754997T>A | CA393170349 | CYP1A2 | c.1460T>A (p.Val487Glu) | |
| 15 | g.74754997T>C | CA393170352 | CYP1A2 | c.1460T>C (p.Val487Ala) | |
| 15 | g.74754997T>G | CA393170355 | CYP1A2 | c.1460T>G (p.Val487Gly) | |
| 15 | g.74754998G>A | CA491489791 | CYP1A2 | c.1461G>A (p.Val487=) | |
| 15 | g.74754998G>C | CA491489792 | CYP1A2 | c.1461G>C (p.Val487=) |