Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.151663761G>A | CA429453134 | NEB | c.5550C>T (p.Ala1850=) | gnomAD v4 |
2 | g.151663761G>C | CA429453135 | NEB | c.5550C>G (p.Ala1850=) | |
2 | g.151663761G>T | CA429453136 | NEB | c.5550C>A (p.Ala1850=) | |
2 | g.151663762G>A | CA348808604 | NEB | c.5549C>T (p.Ala1850Val) | |
2 | g.151663762G>C | CA348808607 | NEB | c.5549C>G (p.Ala1850Gly) | |
2 | g.151663762G>T | CA348808610 | NEB | c.5549C>A (p.Ala1850Asp) | |
2 | g.151663763C>A | CA348808613 | NEB | c.5548G>T (p.Ala1850Ser) | |
2 | g.151663763C>G | CA348808615 | NEB | c.5548G>C (p.Ala1850Pro) | |
2 | g.151663763C>T | CA348808617 | NEB | c.5548G>A (p.Ala1850Thr) | gnomAD v4 |
2 | g.151663764C>A | CA57643646 | NEB | c.5547G>T (p.Val1849=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
2 | g.151663764C= | CA1298286874 | NEB | c.5547G= (p.Val1849=) | |
2 | g.151663764C>G | CA429453137 | NEB | c.5547G>C (p.Val1849=) | |
2 | g.151663764C>T | CA429453138 | NEB | c.5547G>A (p.Val1849=) | |
2 | g.151663765A= | CA1298286875 | NEB | c.5546T= (p.Val1849=) | |
2 | g.151663765A>C | CA348808629 | NEB | c.5546T>G (p.Val1849Gly) | |
2 | g.151663765A>G | CA348808625 | NEB | c.5546T>C (p.Val1849Ala) | dbSNP |
2 | g.151663765A>T | CA348808626 | NEB | c.5546T>A (p.Val1849Glu) | |
2 | g.151663766C>A | CA348808633 | NEB | c.5545G>T (p.Val1849Leu) | gnomAD v4 |
2 | g.151663766C>G | CA348808635 | NEB | c.5545G>C (p.Val1849Leu) | |
2 | g.151663766C>T | CA348808638 | NEB | c.5545G>A (p.Val1849Met) | |
2 | g.151663767T>A | CA348808641 | NEB | c.5544A>T (p.Gln1848His) | |
2 | g.151663767T>C | CA429453139 | NEB | c.5544A>G (p.Gln1848=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
2 | g.151663767T>G | CA348808644 | NEB | c.5544A>C (p.Gln1848His) | gnomAD v4 |
2 | g.151663767T= | CA1298286876 | NEB | c.5544A= (p.Gln1848=) | |
2 | g.151663768T>A | CA348808648 | NEB | c.5543A>T (p.Gln1848Leu) | gnomAD v4 |
2 | g.151663768T>C | CA348808650 | NEB | c.5543A>G (p.Gln1848Arg) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.151663768T>G | CA348808652 | NEB | c.5543A>C (p.Gln1848Pro) | |
2 | g.151663768T= | CA1298286877 | NEB | c.5543A= (p.Gln1848=) | |
2 | g.151663769G>A | CA348808654 | NEB | c.5542C>T (p.Gln1848Ter) | |
2 | g.151663769G>C | CA348808657 | NEB | c.5542C>G (p.Gln1848Glu) | |
2 | g.151663769G>T | CA348808660 | NEB | c.5542C>A (p.Gln1848Lys) | |
2 | g.151663770C>A | CA348808668 | NEB | c.5541G>T (p.Met1847Ile) | |
2 | g.151663770C>G | CA348808666 | NEB | c.5541G>C (p.Met1847Ile) | |
2 | g.151663770C>T | CA348808664 | NEB | c.5541G>A (p.Met1847Ile) | |
2 | g.151663771A>C | CA348808672 | NEB | c.5540T>G (p.Met1847Arg) | |
2 | g.151663771A>G | CA348808676 | NEB | c.5540T>C (p.Met1847Thr) | |
2 | g.151663771A>T | CA348808674 | NEB | c.5540T>A (p.Met1847Lys) | |
2 | g.151663772T>A | CA348808679 | NEB | c.5539A>T (p.Met1847Leu) | |
2 | g.151663772T>C | CA348808682 | NEB | c.5539A>G (p.Met1847Val) | |
2 | g.151663772T>G | CA348808684 | NEB | c.5539A>C (p.Met1847Leu) | |
2 | g.151663773G>A | CA429453143 | NEB | c.5538C>T (p.Phe1846=) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC |
2 | g.151663773G>C | CA348808687 | NEB | c.5538C>G (p.Phe1846Leu) | |
2 | g.151663773G= | CA1298286878 | NEB | c.5538C= (p.Phe1846=) | |
2 | g.151663773G>T | CA348808690 | NEB | c.5538C>A (p.Phe1846Leu) | |
2 | g.151663774A>C | CA348808694 | NEB | c.5537T>G (p.Phe1846Cys) | |
2 | g.151663774A>G | CA348808696 | NEB | c.5537T>C (p.Phe1846Ser) | |
2 | g.151663774A>T | CA348808698 | NEB | c.5537T>A (p.Phe1846Tyr) | |
2 | g.151663775A>C | CA348808701 | NEB | c.5536T>G (p.Phe1846Val) | |
2 | g.151663775A>G | CA348808702 | NEB | c.5536T>C (p.Phe1846Leu) | |
2 | g.151663775A>T | CA348808705 | NEB | c.5536T>A (p.Phe1846Ile) |