Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.151672460_151672481del | CA2549819954 | NEB | c.4188_4209del (p.Gln1397ThrfsTer16) | |
2 | g.151672462A= | CA1298291106 | NEB | c.4206T= (p.Asn1402=) | |
2 | g.151672462A>C | CA348816568 | NEB | c.4206T>G (p.Asn1402Lys) | |
2 | g.151672462A>G | CA429453469 | NEB | c.4206T>C (p.Asn1402=) | ClinVar gnomAD v4 |
2 | g.151672462A>T | CA1910700 | NEB | c.4206T>A (p.Asn1402Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.151672463T>A | CA348816570 | NEB | c.4205A>T (p.Asn1402Ile) | |
2 | g.151672463T>C | CA348816571 | NEB | c.4205A>G (p.Asn1402Ser) | gnomAD v4 |
2 | g.151672463T>G | CA348816569 | NEB | c.4205A>C (p.Asn1402Thr) | |
2 | g.151672464T>A | CA348816573 | NEB | c.4204A>T (p.Asn1402Tyr) | |
2 | g.151672464T>C | CA348816572 | NEB | c.4204A>G (p.Asn1402Asp) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
2 | g.151672464T>G | CA348816574 | NEB | c.4204A>C (p.Asn1402His) | |
2 | g.151672464T= | CA1298291113 | NEB | c.4204A= (p.Asn1402=) | |
2 | g.151672465G>A | CA429453470 | NEB | c.4203C>T (p.Thr1401=) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.151672465G>C | CA429453471 | NEB | c.4203C>G (p.Thr1401=) | |
2 | g.151672465G= | CA1298291118 | NEB | c.4203C= (p.Thr1401=) | |
2 | g.151672465G>T | CA429453472 | NEB | c.4203C>A (p.Thr1401=) | gnomAD v4 |
2 | g.151672466G>A | CA348816575 | NEB | c.4202C>T (p.Thr1401Ile) | |
2 | g.151672466G>C | CA348816576 | NEB | c.4202C>G (p.Thr1401Ser) | |
2 | g.151672466G>T | CA348816577 | NEB | c.4202C>A (p.Thr1401Asn) | |
2 | g.151672467T>A | CA348816578 | NEB | c.4201A>T (p.Thr1401Ser) | |
2 | g.151672467T>C | CA348816579 | NEB | c.4201A>G (p.Thr1401Ala) | |
2 | g.151672467T>G | CA348816580 | NEB | c.4201A>C (p.Thr1401Pro) | |
2 | g.151672468A>C | CA429453475 | NEB | c.4200T>G (p.Ala1400=) | |
2 | g.151672468A>G | CA429453474 | NEB | c.4200T>C (p.Ala1400=) | |
2 | g.151672468A>T | CA429453473 | NEB | c.4200T>A (p.Ala1400=) | gnomAD v4 |
2 | g.151672469G>A | CA348816581 | NEB | c.4199C>T (p.Ala1400Val) | |
2 | g.151672469G>C | CA348816582 | NEB | c.4199C>G (p.Ala1400Gly) | gnomAD v4 |
2 | g.151672469G>T | CA348816583 | NEB | c.4199C>A (p.Ala1400Asp) | |
2 | g.151672470C>A | CA348816584 | NEB | c.4198G>T (p.Ala1400Ser) | gnomAD v4 |
2 | g.151672470C= | CA1298291125 | NEB | c.4198G= (p.Ala1400=) | |
2 | g.151672470C>G | CA348816585 | NEB | c.4198G>C (p.Ala1400Pro) | |
2 | g.151672470C>T | CA358031 | NEB | c.4198G>A (p.Ala1400Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.151672471G>A | CA1910701 | NEB | c.4197C>T (p.Val1399=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC |
2 | g.151672471G>C | CA429453476 | NEB | c.4197C>G (p.Val1399=) | |
2 | g.151672471G= | CA1298291134 | NEB | c.4197C= (p.Val1399=) | |
2 | g.151672471G>T | CA429453477 | NEB | c.4197C>A (p.Val1399=) | |
2 | g.151672472A= | CA1298291140 | NEB | c.4196T= (p.Val1399=) | |
2 | g.151672472A>C | CA348816586 | NEB | c.4196T>G (p.Val1399Gly) | |
2 | g.151672472A>G | CA348816588 | NEB | c.4196T>C (p.Val1399Ala) | gnomAD v4 |
2 | g.151672472A>T | CA348816587 | NEB | c.4196T>A (p.Val1399Asp) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.151672473C>A | CA348816589 | NEB | c.4195G>T (p.Val1399Phe) | |
2 | g.151672473C>G | CA348816590 | NEB | c.4195G>C (p.Val1399Leu) | |
2 | g.151672473C>T | CA348816591 | NEB | c.4195G>A (p.Val1399Ile) | gnomAD v4 |
2 | g.151672474A>C | CA348816592 | NEB | c.4194T>G (p.Asp1398Glu) | |
2 | g.151672474A>G | CA429453478 | NEB | c.4194T>C (p.Asp1398=) | |
2 | g.151672474A>T | CA348816593 | NEB | c.4194T>A (p.Asp1398Glu) | |
2 | g.151672475T>A | CA348816594 | NEB | c.4193A>T (p.Asp1398Val) | gnomAD v4 |
2 | g.151672475T>C | CA348816595 | NEB | c.4193A>G (p.Asp1398Gly) | dbSNP gnomAD v4 |
2 | g.151672475T>G | CA348816596 | NEB | c.4193A>C (p.Asp1398Ala) | |
2 | g.151672475T= | CA1298291144 | NEB | c.4193A= (p.Asp1398=) |