Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.108561698G>A | CA365338634 | FOXO3 | c.490G>A (p.Asp164Asn) | |
6 | g.108561698G>C | CA365338632 | FOXO3 | c.490G>C (p.Asp164His) | |
6 | g.108561698G>T | CA365338633 | FOXO3 | c.490G>T (p.Asp164Tyr) | |
6 | g.108561699A>C | CA365338635 | FOXO3 | c.491A>C (p.Asp164Ala) | |
6 | g.108561699A>G | CA365338636 | FOXO3 | c.491A>G (p.Asp164Gly) | |
6 | g.108561699A>T | CA365338637 | FOXO3 | c.491A>T (p.Asp164Val) | |
6 | g.108561700C>A | CA365338638 | FOXO3 | c.492C>A (p.Asp164Glu) | |
6 | g.108561700C>G | CA365338639 | FOXO3 | c.492C>G (p.Asp164Glu) | |
6 | g.108561700C>T | CA451920501 | FOXO3 | c.492C>T (p.Asp164=) | gnomAD v4 COSMIC |
6 | g.108561701C>A | CA365338640 | FOXO3 | c.493C>A (p.Leu165Met) | |
6 | g.108561701C= | CA1654338363 | FOXO3 | c.493C= (p.Leu165=) | |
6 | g.108561701C>G | CA365338641 | FOXO3 | c.493C>G (p.Leu165Val) | |
6 | g.108561701C>T | CA3949235 | FOXO3 | c.493C>T (p.Leu165=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.108561702T>A | CA365338642 | FOXO3 | c.494T>A (p.Leu165Gln) | |
6 | g.108561702T>C | CA365338643 | FOXO3 | c.494T>C (p.Leu165Pro) | |
6 | g.108561702T>G | CA365338644 | FOXO3 | c.494T>G (p.Leu165Arg) | |
6 | g.108561703G>A | CA3949237 | FOXO3 | c.495G>A (p.Leu165=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.108561703G>C | CA3949236 | FOXO3 | c.495G>C (p.Leu165=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.108561703G= | CA1654338366 | FOXO3 | c.495G= (p.Leu165=) | |
6 | g.108561703G>T | CA451920507 | FOXO3 | c.495G>T (p.Leu165=) | COSMIC |
6 | g.108561704_108561779dup | CA2679911224 | FOXO3 | c.496_571dup (p.Val191AspfsTer32) | gnomAD v4 |
6 | g.108561704A>C | CA365338645 | FOXO3 | c.496A>C (p.Ile166Leu) | |
6 | g.108561704A>G | CA365338647 | FOXO3 | c.496A>G (p.Ile166Val) | |
6 | g.108561704A>T | CA365338646 | FOXO3 | c.496A>T (p.Ile166Phe) | |
6 | g.108561705T>A | CA365338648 | FOXO3 | c.497T>A (p.Ile166Asn) | |
6 | g.108561705T>C | CA365338649 | FOXO3 | c.497T>C (p.Ile166Thr) | |
6 | g.108561705T>G | CA365338650 | FOXO3 | c.497T>G (p.Ile166Ser) | |
6 | g.108561706C>A | CA451920513 | FOXO3 | c.498C>A (p.Ile166=) | dbSNP gnomAD v2 gnomAD v4 |
6 | g.108561706C= | CA1654338370 | FOXO3 | c.498C= (p.Ile166=) | |
6 | g.108561706C>G | CA365338651 | FOXO3 | c.498C>G (p.Ile166Met) | |
6 | g.108561706C>T | CA451920512 | FOXO3 | c.498C>T (p.Ile166=) | |
6 | g.108561707A>C | CA365338652 | FOXO3 | c.499A>C (p.Thr167Pro) | |
6 | g.108561707A>G | CA365338653 | FOXO3 | c.499A>G (p.Thr167Ala) | |
6 | g.108561707A>T | CA365338654 | FOXO3 | c.499A>T (p.Thr167Ser) | |
6 | g.108561708C>A | CA365338655 | FOXO3 | c.500C>A (p.Thr167Asn) | |
6 | g.108561708C= | CA1654338378 | FOXO3 | c.500C= (p.Thr167=) | |
6 | g.108561708C>G | CA365338656 | FOXO3 | c.500C>G (p.Thr167Ser) | |
6 | g.108561708C>T | CA365338657 | FOXO3 | c.500C>T (p.Thr167Ile) | dbSNP gnomAD v4 |
6 | g.108561709C>A | CA451920517 | FOXO3 | c.501C>A (p.Thr167=) | |
6 | g.108561709C>G | CA451920519 | FOXO3 | c.501C>G (p.Thr167=) | |
6 | g.108561709C>T | CA451920518 | FOXO3 | c.501C>T (p.Thr167=) | |
6 | g.108561710C>A | CA365338658 | FOXO3 | c.502C>A (p.Arg168Ser) | |
6 | g.108561710C>G | CA365338659 | FOXO3 | c.502C>G (p.Arg168Gly) | gnomAD v4 |
6 | g.108561710C>T | CA365338660 | FOXO3 | c.502C>T (p.Arg168Cys) | gnomAD v4 |
6 | g.108561711G>A | CA3949238 | FOXO3 | c.503G>A (p.Arg168His) | dbSNP ExAC gnomAD v2 COSMIC |
6 | g.108561711G>C | CA365338661 | FOXO3 | c.503G>C (p.Arg168Pro) | |
6 | g.108561711G= | CA1654338381 | FOXO3 | c.503G= (p.Arg168=) | |
6 | g.108561711G>T | CA365338662 | FOXO3 | c.503G>T (p.Arg168Leu) | gnomAD v4 |
6 | g.108561712C>A | CA451920521 | FOXO3 | c.504C>A (p.Arg168=) | |
6 | g.108561712C= | CA1654338394 | FOXO3 | c.504C= (p.Arg168=) |