Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.120840029C>A | CA457397855 | TSPAN12 | c.147G>T (p.Thr49=) | |
7 | g.120840029C= | CA1738882808 | TSPAN12 | c.147G= (p.Thr49=) | |
7 | g.120840029C>G | CA457397856 | TSPAN12 | c.147G>C (p.Thr49=) | |
7 | g.120840029C>T | CA4453992 | TSPAN12 | c.147G>A (p.Thr49=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
7 | g.120840030G>A | CA269454 | TSPAN12 | c.146C>T (p.Thr49Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.120840030G>C | CA369141471 | TSPAN12 | c.146C>G (p.Thr49Arg) | |
7 | g.120840030G= | CA1738882809 | TSPAN12 | c.146C= (p.Thr49=) | |
7 | g.120840030G>T | CA4453993 | TSPAN12 | c.146C>A (p.Thr49Lys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.120840031T>A | CA369141474 | TSPAN12 | c.145A>T (p.Thr49Ser) | |
7 | g.120840031T>C | CA369141473 | TSPAN12 | c.145A>G (p.Thr49Ala) | ClinVar |
7 | g.120840031T>G | CA369141472 | TSPAN12 | c.145A>C (p.Thr49Pro) | |
7 | g.120840033del | CA2684648852 | TSPAN12 | c.145del (p.Thr49ArgfsTer3) | gnomAD v4 |
7 | g.120840032T>A | CA369141475 | TSPAN12 | c.144A>T (p.Glu48Asp) | |
7 | g.120840032T>C | CA457397858 | TSPAN12 | c.144A>G (p.Glu48=) | dbSNP gnomAD v4 |
7 | g.120840032T>G | CA369141476 | TSPAN12 | c.144A>C (p.Glu48Asp) | |
7 | g.120840032T= | CA1738882810 | TSPAN12 | c.144A= (p.Glu48=) | |
7 | g.120840033T>A | CA369141477 | TSPAN12 | c.143A>T (p.Glu48Val) | |
7 | g.120840033T>C | CA369141478 | TSPAN12 | c.143A>G (p.Glu48Gly) | |
7 | g.120840033T>G | CA369141479 | TSPAN12 | c.143A>C (p.Glu48Ala) | |
7 | g.120840034C>A | CA369141480 | TSPAN12 | c.142G>T (p.Glu48Ter) | |
7 | g.120840034C>G | CA369141481 | TSPAN12 | c.142G>C (p.Glu48Gln) | |
7 | g.120840034C>T | CA369141482 | TSPAN12 | c.142G>A (p.Glu48Lys) | |
7 | g.120840035T>A | CA457397862 | TSPAN12 | c.141A>T (p.Ala47=) | |
7 | g.120840035T>C | CA4453994 | TSPAN12 | c.141A>G (p.Ala47=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.120840035T>G | CA457397863 | TSPAN12 | c.141A>C (p.Ala47=) | |
7 | g.120840035T= | CA1738882811 | TSPAN12 | c.141A= (p.Ala47=) | |
7 | g.120840036G>A | CA369141483 | TSPAN12 | c.140C>T (p.Ala47Val) | gnomAD v4 |
7 | g.120840036G>C | CA369141484 | TSPAN12 | c.140C>G (p.Ala47Gly) | |
7 | g.120840036G>T | CA369141485 | TSPAN12 | c.140C>A (p.Ala47Glu) | gnomAD v4 |
7 | g.120840037C>A | CA369141488 | TSPAN12 | c.139G>T (p.Ala47Ser) | dbSNP gnomAD v2 |
7 | g.120840037C= | CA1738882812 | TSPAN12 | c.139G= (p.Ala47=) | |
7 | g.120840037C>G | CA369141487 | TSPAN12 | c.139G>C (p.Ala47Pro) | |
7 | g.120840037C>T | CA369141486 | TSPAN12 | c.139G>A (p.Ala47Thr) | gnomAD v4 |
7 | g.120840038A>C | CA457397864 | TSPAN12 | c.138T>G (p.Thr46=) | |
7 | g.120840038A>G | CA457397865 | TSPAN12 | c.138T>C (p.Thr46=) | |
7 | g.120840038A>T | CA457397866 | TSPAN12 | c.138T>A (p.Thr46=) | |
7 | g.120840039G>A | CA369141489 | TSPAN12 | c.137C>T (p.Thr46Ile) | |
7 | g.120840039G>C | CA369141490 | TSPAN12 | c.137C>G (p.Thr46Ser) | |
7 | g.120840039G>T | CA369141491 | TSPAN12 | c.137C>A (p.Thr46Asn) | |
7 | g.120840040T>A | CA369141492 | TSPAN12 | c.136A>T (p.Thr46Ser) | |
7 | g.120840040T>C | CA369141493 | TSPAN12 | c.136A>G (p.Thr46Ala) | |
7 | g.120840040T>G | CA369141494 | TSPAN12 | c.136A>C (p.Thr46Pro) | |
7 | g.120840041T>A | CA369141495 | TSPAN12 | c.135A>T (p.Leu45Phe) | |
7 | g.120840041T>C | CA457397868 | TSPAN12 | c.135A>G (p.Leu45=) | |
7 | g.120840041T>G | CA369141496 | TSPAN12 | c.135A>C (p.Leu45Phe) | |
7 | g.120840042A>C | CA369141497 | TSPAN12 | c.134T>G (p.Leu45Ter) | |
7 | g.120840042A>G | CA369141498 | TSPAN12 | c.134T>C (p.Leu45Ser) | |
7 | g.120840042A>T | CA369141499 | TSPAN12 | c.134T>A (p.Leu45Ter) | |
7 | g.120840043A>C | CA369141500 | TSPAN12 | c.133T>G (p.Leu45Val) | gnomAD v4 |
7 | g.120840043A>G | CA457397870 | TSPAN12 | c.133T>C (p.Leu45=) |