| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.54465697T>A | CA413244292 | FGD1 | c.1496A>T (p.Gln499Leu) | |
| X | g.54465697T>C | CA413244297 | FGD1 | c.1496A>G (p.Gln499Arg) | |
| X | g.54465697T>G | CA413244291 | FGD1 | c.1496A>C (p.Gln499Pro) | |
| X | g.54465698G>A | CA413244305 | FGD1 | c.1495C>T (p.Gln499Ter) | |
| X | g.54465698G>C | CA413244302 | FGD1 | c.1495C>G (p.Gln499Glu) | |
| X | g.54465698G>T | CA413244309 | FGD1 | c.1495C>A (p.Gln499Lys) | |
| X | g.54465699C>A | CA516689347 | FGD1 | c.1494G>T (p.Val498=) | |
| X | g.54465699C>G | CA516689348 | FGD1 | c.1494G>C (p.Val498=) | |
| X | g.54465699C>T | CA516689349 | FGD1 | c.1494G>A (p.Val498=) | |
| X | g.54465700A>C | CA413244311 | FGD1 | c.1493T>G (p.Val498Gly) | |
| X | g.54465700A>G | CA413244314 | FGD1 | c.1493T>C (p.Val498Ala) | |
| X | g.54465700A>T | CA413244320 | FGD1 | c.1493T>A (p.Val498Glu) | |
| X | g.54465701C>A | CA413244324 | FGD1 | c.1492G>T (p.Val498Leu) | |
| X | g.54465701C>G | CA413244328 | FGD1 | c.1492G>C (p.Val498Leu) | |
| X | g.54465701C>T | CA413244330 | FGD1 | c.1492G>A (p.Val498Met) | |
| X | g.54465702C>A | CA413244332 | FGD1 | c.1491G>T (p.Glu497Asp) | |
| X | g.54465702C>G | CA413244333 | FGD1 | c.1491G>C (p.Glu497Asp) | |
| X | g.54465702C>T | CA516689353 | FGD1 | c.1491G>A (p.Glu497=) | |
| X | g.54465703T>A | CA413244334 | FGD1 | c.1490A>T (p.Glu497Val) | |
| X | g.54465703T>C | CA413244335 | FGD1 | c.1490A>G (p.Glu497Gly) | |
| X | g.54465703T>G | CA413244338 | FGD1 | c.1490A>C (p.Glu497Ala) | |
| X | g.54465704C>A | CA413244347 | FGD1 | c.1489G>T (p.Glu497Ter) | |
| X | g.54465704C>G | CA413244346 | FGD1 | c.1489G>C (p.Glu497Gln) | |
| X | g.54465704C>T | CA413244343 | FGD1 | c.1489G>A (p.Glu497Lys) | |
| X | g.54465705A>C | CA413244349 | FGD1 | c.1488T>G (p.His496Gln) | gnomAD v4 |
| X | g.54465705A>G | CA516689358 | FGD1 | c.1488T>C (p.His496=) | gnomAD v4 |
| X | g.54465705A>T | CA413244351 | FGD1 | c.1488T>A (p.His496Gln) | gnomAD v4 |
| X | g.54465706T>A | CA413244353 | FGD1 | c.1487A>T (p.His496Leu) | |
| X | g.54465706T>C | CA413244356 | FGD1 | c.1487A>G (p.His496Arg) | dbSNP gnomAD v4 |
| X | g.54465706T>G | CA413244362 | FGD1 | c.1487A>C (p.His496Pro) | |
| X | g.54465706T= | CA2430188897 | FGD1 | c.1487A= (p.His496=) | |
| X | g.54465707G>A | CA413244365 | FGD1 | c.1486C>T (p.His496Tyr) | |
| X | g.54465707G>C | CA413244368 | FGD1 | c.1486C>G (p.His496Asp) | COSMIC |
| X | g.54465707G>T | CA413244371 | FGD1 | c.1486C>A (p.His496Asn) | |
| X | g.54465708G>A | CA516689362 | FGD1 | c.1485C>T (p.Ile495=) | COSMIC |
| X | g.54465708G>C | CA413244376 | FGD1 | c.1485C>G (p.Ile495Met) | |
| X | g.54465708G>T | CA516689361 | FGD1 | c.1485C>A (p.Ile495=) | |
| X | g.54465709A>C | CA413244378 | FGD1 | c.1484T>G (p.Ile495Ser) | |
| X | g.54465709A>G | CA413244389 | FGD1 | c.1484T>C (p.Ile495Thr) | |
| X | g.54465709A>T | CA413244392 | FGD1 | c.1484T>A (p.Ile495Asn) | |
| X | g.54465710T>A | CA413244396 | FGD1 | c.1483A>T (p.Ile495Phe) | |
| X | g.54465710T>C | CA413244397 | FGD1 | c.1483A>G (p.Ile495Val) | gnomAD v4 |
| X | g.54465710T>G | CA413244394 | FGD1 | c.1483A>C (p.Ile495Leu) | |
| X | g.54465711G>A | CA516689367 | FGD1 | c.1482C>T (p.Ile494=) | |
| X | g.54465711G>C | CA413244399 | FGD1 | c.1482C>G (p.Ile494Met) | |
| X | g.54465711G>T | CA516689368 | FGD1 | c.1482C>A (p.Ile494=) | |
| X | g.54465712A>C | CA413244402 | FGD1 | c.1481T>G (p.Ile494Ser) | |
| X | g.54465712A>G | CA413244405 | FGD1 | c.1481T>C (p.Ile494Thr) | |
| X | g.54465712A>T | CA413244407 | FGD1 | c.1481T>A (p.Ile494Asn) | |
| X | g.54465713T>A | CA413244410 | FGD1 | c.1480A>T (p.Ile494Phe) |