| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.125317657A>C | CA358117504 | FAT4 | c.1246A>C (p.Asn416His) c.-55+1680A>C (n.-55+1680A>C) | |
| 4 | g.125317657A>G | CA358117506 | FAT4 | c.1246A>G (p.Asn416Asp) c.-55+1680A>G (n.-55+1680A>G) | |
| 4 | g.125317657A>T | CA358117505 | FAT4 | c.1246A>T (p.Asn416Tyr) c.-55+1680A>T (n.-55+1680A>T) | |
| 4 | g.125317658A>C | CA358117507 | FAT4 | c.1247A>C (p.Asn416Thr) c.-55+1681A>C (n.-55+1681A>C) | |
| 4 | g.125317658A>G | CA358117508 | FAT4 | c.1247A>G (p.Asn416Ser) c.-55+1681A>G (n.-55+1681A>G) | |
| 4 | g.125317658A>T | CA358117509 | FAT4 | c.1247A>T (p.Asn416Ile) c.-55+1681A>T (n.-55+1681A>T) | |
| 4 | g.125317659C>A | CA358117510 | FAT4 | c.1248C>A (p.Asn416Lys) c.-55+1682C>A (n.-55+1682C>A) | |
| 4 | g.125317659C= | CA1491600381 | FAT4 | c.1248C= (p.Asn416=) c.-55+1682C= (n.-55+1682C=) | |
| 4 | g.125317659C>G | CA358117511 | FAT4 | c.1248C>G (p.Asn416Lys) c.-55+1682C>G (n.-55+1682C>G) | |
| 4 | g.125317659C>T | CA3071948 | FAT4 | c.1248C>T (p.Asn416=) c.-55+1682C>T (n.-55+1682C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.125317660C>A | CA358117512 | FAT4 | c.1249C>A (p.Leu417Met) c.-55+1683C>A (n.-55+1683C>A) | |
| 4 | g.125317660C= | CA1491600394 | FAT4 | c.1249C= (p.Leu417=) c.-55+1683C= (n.-55+1683C=) | |
| 4 | g.125317660C>G | CA358117513 | FAT4 | c.1249C>G (p.Leu417Val) c.-55+1683C>G (n.-55+1683C>G) | |
| 4 | g.125317660C>T | CA441366916 | FAT4 | c.1249C>T (p.Leu417=) c.-55+1683C>T (n.-55+1683C>T) | dbSNP |
| 4 | g.125317661T>A | CA358117514 | FAT4 | c.1250T>A (p.Leu417Gln) c.-55+1684T>A (n.-55+1684T>A) | |
| 4 | g.125317661T>C | CA358117515 | FAT4 | c.1250T>C (p.Leu417Pro) c.-55+1684T>C (n.-55+1684T>C) | dbSNP |
| 4 | g.125317661T>G | CA358117516 | FAT4 | c.1250T>G (p.Leu417Arg) c.-55+1684T>G (n.-55+1684T>G) | |
| 4 | g.125317661T= | CA1491600403 | FAT4 | c.1250T= (p.Leu417=) c.-55+1684T= (n.-55+1684T=) | |
| 4 | g.125317662G>A | CA441366922 | FAT4 | c.1251G>A (p.Leu417=) c.-55+1685G>A (n.-55+1685G>A) | |
| 4 | g.125317662G>C | CA441366920 | FAT4 | c.1251G>C (p.Leu417=) c.-55+1685G>C (n.-55+1685G>C) | |
| 4 | g.125317662G>T | CA441366918 | FAT4 | c.1251G>T (p.Leu417=) c.-55+1685G>T (n.-55+1685G>T) | |
| 4 | g.125317663A= | CA1491600407 | FAT4 | c.1252A= (p.Ser418=) c.-55+1686A= (n.-55+1686A=) | |
| 4 | g.125317663A>C | CA358117519 | FAT4 | c.1252A>C (p.Ser418Arg) c.-55+1686A>C (n.-55+1686A>C) | |
| 4 | g.125317663A>G | CA358117518 | FAT4 | c.1252A>G (p.Ser418Gly) c.-55+1686A>G (n.-55+1686A>G) | |
| 4 | g.125317663A>T | CA358117517 | FAT4 | c.1252A>T (p.Ser418Cys) c.-55+1686A>T (n.-55+1686A>T) | dbSNP |
| 4 | g.125317664G>A | CA358117520 | FAT4 | c.1253G>A (p.Ser418Asn) c.-55+1687G>A (n.-55+1687G>A) | |
| 4 | g.125317664G>C | CA104862100 | FAT4 | c.1253G>C (p.Ser418Thr) c.-55+1687G>C (n.-55+1687G>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.125317664G= | CA1491600418 | FAT4 | c.1253G= (p.Ser418=) c.-55+1687G= (n.-55+1687G=) | |
| 4 | g.125317664G>T | CA358117521 | FAT4 | c.1253G>T (p.Ser418Ile) c.-55+1687G>T (n.-55+1687G>T) | dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.125317665C>A | CA358117522 | FAT4 | c.1254C>A (p.Ser418Arg) c.-55+1688C>A (n.-55+1688C>A) | |
| 4 | g.125317665C= | CA1491600426 | FAT4 | c.1254C= (p.Ser418=) c.-55+1688C= (n.-55+1688C=) | |
| 4 | g.125317665C>G | CA358117523 | FAT4 | c.1254C>G (p.Ser418Arg) c.-55+1688C>G (n.-55+1688C>G) | |
| 4 | g.125317665C>T | CA3071949 | FAT4 | c.1254C>T (p.Ser418=) c.-55+1688C>T (n.-55+1688C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
| 4 | g.125317666C>A | CA358117524 | FAT4 | c.1255C>A (p.Leu419Ile) c.-55+1689C>A (n.-55+1689C>A) | |
| 4 | g.125317666C>G | CA358117525 | FAT4 | c.1255C>G (p.Leu419Val) c.-55+1689C>G (n.-55+1689C>G) | |
| 4 | g.125317666C>T | CA441366940 | FAT4 | c.1255C>T (p.Leu419=) c.-55+1689C>T (n.-55+1689C>T) | gnomAD v4 |
| 4 | g.125317667T>A | CA358117526 | FAT4 | c.1256T>A (p.Leu419Gln) c.-55+1690T>A (n.-55+1690T>A) | |
| 4 | g.125317667T>C | CA358117527 | FAT4 | c.1256T>C (p.Leu419Pro) c.-55+1690T>C (n.-55+1690T>C) | COSMIC COSMIC |
| 4 | g.125317667T>G | CA358117528 | FAT4 | c.1256T>G (p.Leu419Arg) c.-55+1690T>G (n.-55+1690T>G) | |
| 4 | g.125317668A= | CA1491600436 | FAT4 | c.1257A= (p.Leu419=) c.-55+1691A= (n.-55+1691A=) | |
| 4 | g.125317668A>C | CA441366943 | FAT4 | c.1257A>C (p.Leu419=) c.-55+1691A>C (n.-55+1691A>C) | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.125317668A>G | CA441366945 | FAT4 | c.1257A>G (p.Leu419=) c.-55+1691A>G (n.-55+1691A>G) | gnomAD v4 |
| 4 | g.125317668A>T | CA441366944 | FAT4 | c.1257A>T (p.Leu419=) c.-55+1691A>T (n.-55+1691A>T) | |
| 4 | g.125317669A>C | CA358117531 | FAT4 | c.1258A>C (p.Ile420Leu) c.-55+1692A>C (n.-55+1692A>C) | |
| 4 | g.125317669A>G | CA358117530 | FAT4 | c.1258A>G (p.Ile420Val) c.-55+1692A>G (n.-55+1692A>G) | ClinVar dbSNP gnomAD v4 |
| 4 | g.125317669A>T | CA358117529 | FAT4 | c.1258A>T (p.Ile420Phe) c.-55+1692A>T (n.-55+1692A>T) | |
| 4 | g.125317670T>A | CA358117532 | FAT4 | c.1259T>A (p.Ile420Asn) c.-55+1693T>A (n.-55+1693T>A) | |
| 4 | g.125317670T>C | CA358117533 | FAT4 | c.1259T>C (p.Ile420Thr) c.-55+1693T>C (n.-55+1693T>C) | |
| 4 | g.125317670T>G | CA358117534 | FAT4 | c.1259T>G (p.Ile420Ser) c.-55+1693T>G (n.-55+1693T>G) | |
| 4 | g.125317671C>A | CA441366947 | FAT4 | c.1260C>A (p.Ile420=) c.-55+1694C>A (n.-55+1694C>A) |