Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.82750625T>A | CA401621842 | FN3K | c.800T>A (p.Ile267Asn) c.650T>A (p.Ile217Asn) | |
17 | g.82750625T>C | CA401621843 | FN3K | c.800T>C (p.Ile267Thr) c.650T>C (p.Ile217Thr) | |
17 | g.82750625T>G | CA401621844 | FN3K | c.800T>G (p.Ile267Ser) c.650T>G (p.Ile217Ser) | |
17 | g.82750625T= | CA2279185691 | FN3K | c.800T= (p.Ile267=) c.650T= (p.Ile217=) | |
17 | g.82750626C>A | CA502803453 | FN3K | c.801C>A (p.Ile267=) c.651C>A (p.Ile217=) | |
17 | g.82750626C= | CA2279185693 | FN3K | c.801C= (p.Ile267=) c.651C= (p.Ile217=) | |
17 | g.82750626C>G | CA401621845 | FN3K | c.801C>G (p.Ile267Met) c.651C>G (p.Ile217Met) | |
17 | g.82750626C>T | CA8861418 | FN3K | c.801C>T (p.Ile267=) c.651C>T (p.Ile217=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.82750629dup | CA2279185692 | FN3K | c.804dup (p.Lys269GlnfsTer16) c.654dup (p.Lys219GlnfsTer16) | dbSNP |
17 | g.82750627C>A | CA401621846 | FN3K | c.802C>A (p.Pro268Thr) c.652C>A (p.Pro218Thr) | |
17 | g.82750627C= | CA2279185694 | FN3K | c.802C= (p.Pro268=) c.652C= (p.Pro218=) | |
17 | g.82750627C>G | CA401621847 | FN3K | c.802C>G (p.Pro268Ala) c.652C>G (p.Pro218Ala) | |
17 | g.82750627C>T | CA401621848 | FN3K | c.802C>T (p.Pro268Ser) c.652C>T (p.Pro218Ser) | dbSNP gnomAD v4 |
17 | g.82750628C>A | CA295246313 | FN3K | c.803C>A (p.Pro268His) c.653C>A (p.Pro218His) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.82750628C= | CA2279185695 | FN3K | c.803C= (p.Pro268=) c.653C= (p.Pro218=) | |
17 | g.82750628C>G | CA401621850 | FN3K | c.803C>G (p.Pro268Arg) c.653C>G (p.Pro218Arg) | gnomAD v4 |
17 | g.82750628C>T | CA401621849 | FN3K | c.803C>T (p.Pro268Leu) c.653C>T (p.Pro218Leu) | gnomAD v4 |
17 | g.82750629C>A | CA502803458 | FN3K | c.804C>A (p.Pro268=) c.654C>A (p.Pro218=) | dbSNP |
17 | g.82750629C= | CA2279185696 | FN3K | c.804C= (p.Pro268=) c.654C= (p.Pro218=) | |
17 | g.82750629C>G | CA502803459 | FN3K | c.804C>G (p.Pro268=) c.654C>G (p.Pro218=) | gnomAD v4 |
17 | g.82750629C>T | CA502803460 | FN3K | c.804C>T (p.Pro268=) c.654C>T (p.Pro218=) | gnomAD v4 |
17 | g.82750630A>C | CA401621853 | FN3K | c.805A>C (p.Lys269Gln) c.655A>C (p.Lys219Gln) | |
17 | g.82750630A>G | CA401621851 | FN3K | c.805A>G (p.Lys269Glu) c.655A>G (p.Lys219Glu) | |
17 | g.82750630A>T | CA401621852 | FN3K | c.805A>T (p.Lys269Ter) c.655A>T (p.Lys219Ter) | |
17 | g.82750630_82750631insCAAACCCAAACACACCCAACAC | CA2810674690 | FN3K | c.805_806insCAAACCCAAACACACCCAACAC (p.Lys269ThrfsTer23) c.655_656insCAAACCCAAACACACCCAACAC (p.Lys219ThrfsTer23) | |
17 | g.82750631A>C | CA401621854 | FN3K | c.806A>C (p.Lys269Thr) c.656A>C (p.Lys219Thr) | |
17 | g.82750631A>G | CA401621855 | FN3K | c.806A>G (p.Lys269Arg) c.656A>G (p.Lys219Arg) | |
17 | g.82750631A>T | CA401621856 | FN3K | c.806A>T (p.Lys269Met) c.656A>T (p.Lys219Met) | |
17 | g.82750632G>A | CA502803461 | FN3K | c.807G>A (p.Lys269=) c.657G>A (p.Lys219=) | gnomAD v4 |
17 | g.82750632G>C | CA401621857 | FN3K | c.807G>C (p.Lys269Asn) c.657G>C (p.Lys219Asn) | dbSNP |
17 | g.82750632G= | CA2279185697 | FN3K | c.807G= (p.Lys269=) c.657G= (p.Lys219=) | |
17 | g.82750632G>T | CA401621858 | FN3K | c.807G>T (p.Lys269Asn) c.657G>T (p.Lys219Asn) | COSMIC |
17 | g.82750633G>A | CA401621859 | FN3K | c.808G>A (p.Ala270Thr) c.658G>A (p.Ala220Thr) | |
17 | g.82750633G>C | CA401621860 | FN3K | c.808G>C (p.Ala270Pro) c.658G>C (p.Ala220Pro) | |
17 | g.82750633G>T | CA401621861 | FN3K | c.808G>T (p.Ala270Ser) c.658G>T (p.Ala220Ser) | |
17 | g.82750634C>A | CA401621862 | FN3K | c.809C>A (p.Ala270Asp) c.659C>A (p.Ala220Asp) | |
17 | g.82750634C>G | CA401621863 | FN3K | c.809C>G (p.Ala270Gly) c.659C>G (p.Ala220Gly) | |
17 | g.82750634C>T | CA401621864 | FN3K | c.809C>T (p.Ala270Val) c.659C>T (p.Ala220Val) | gnomAD v4 |
17 | g.82750635T>A | CA502803462 | FN3K | c.810T>A (p.Ala270=) c.660T>A (p.Ala220=) | |
17 | g.82750635T>C | CA502803463 | FN3K | c.810T>C (p.Ala270=) c.660T>C (p.Ala220=) | |
17 | g.82750635T>G | CA502803465 | FN3K | c.810T>G (p.Ala270=) c.660T>G (p.Ala220=) | |
17 | g.82750636C>A | CA401621866 | FN3K | c.811C>A (p.Pro271Thr) c.661C>A (p.Pro221Thr) | |
17 | g.82750636C= | CA2279185698 | FN3K | c.811C= (p.Pro271=) c.661C= (p.Pro221=) | |
17 | g.82750636C>G | CA8861419 | FN3K | c.811C>G (p.Pro271Ala) c.661C>G (p.Pro221Ala) | dbSNP ExAC gnomAD v4 |
17 | g.82750636C>T | CA401621865 | FN3K | c.811C>T (p.Pro271Ser) c.661C>T (p.Pro221Ser) | COSMIC |
17 | g.82750637C>A | CA401621867 | FN3K | c.812C>A (p.Pro271Gln) c.662C>A (p.Pro221Gln) | |
17 | g.82750637C= | CA2279185699 | FN3K | c.812C= (p.Pro271=) c.662C= (p.Pro221=) | |
17 | g.82750637C>G | CA401621868 | FN3K | c.812C>G (p.Pro271Arg) c.662C>G (p.Pro221Arg) | |
17 | g.82750637C>T | CA8861420 | FN3K | c.812C>T (p.Pro271Leu) c.662C>T (p.Pro221Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.82750638G>A | CA8861421 | FN3K | c.813G>A (p.Pro271=) c.663G>A (p.Pro221=) | dbSNP ExAC gnomAD v2 gnomAD v4 |