Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.151672460_151672481del | CA2549819954 | NEB | c.4188_4209del (p.Gln1397ThrfsTer16) | |
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=) | |
2 | g.151672476C>A | CA348816597 | NEB | c.4192G>T (p.Asp1398Tyr) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
2 | g.151672476C= | CA1298291147 | NEB | c.4192G= (p.Asp1398=) | |
2 | g.151672476C>G | CA348816598 | NEB | c.4192G>C (p.Asp1398His) | |
2 | g.151672476C>T | CA348816599 | NEB | c.4192G>A (p.Asp1398Asn) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.151672477C>A | CA348816601 | NEB | c.4191G>T (p.Gln1397His) | |
2 | g.151672477C>G | CA348816600 | NEB | c.4191G>C (p.Gln1397His) | gnomAD v4 |
2 | g.151672477C>T | CA429453479 | NEB | c.4191G>A (p.Gln1397=) | |
2 | g.151672478T>A | CA348816602 | NEB | c.4190A>T (p.Gln1397Leu) | |
2 | g.151672478T>C | CA348816603 | NEB | c.4190A>G (p.Gln1397Arg) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.151672478T>G | CA348816604 | NEB | c.4190A>C (p.Gln1397Pro) | |
2 | g.151672478T= | CA1298291150 | NEB | c.4190A= (p.Gln1397=) | |
2 | g.151672479G>A | CA348816605 | NEB | c.4189C>T (p.Gln1397Ter) | |
2 | g.151672479G>C | CA348816606 | NEB | c.4189C>G (p.Gln1397Glu) | dbSNP |
2 | g.151672479G= | CA1298291154 | NEB | c.4189C= (p.Gln1397=) | |
2 | g.151672479G>T | CA348816607 | NEB | c.4189C>A (p.Gln1397Lys) | gnomAD v4 |
2 | g.151672480G>A | CA429453480 | NEB | c.4188C>T (p.Ala1396=) | |
2 | g.151672480G>C | CA429453482 | NEB | c.4188C>G (p.Ala1396=) | |
2 | g.151672480G>T | CA429453481 | NEB | c.4188C>A (p.Ala1396=) | COSMIC COSMIC COSMIC |
2 | g.151672481G>A | CA1910702 | NEB | c.4187C>T (p.Ala1396Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.151672481G>C | CA348816609 | NEB | c.4187C>G (p.Ala1396Gly) | |
2 | g.151672481G= | CA1298291158 | NEB | c.4187C= (p.Ala1396=) | |
2 | g.151672481G>T | CA348816608 | NEB | c.4187C>A (p.Ala1396Asp) | |
2 | g.151672482C>A | CA1910703 | NEB | c.4186G>T (p.Ala1396Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.151672482C= | CA1298291162 | NEB | c.4186G= (p.Ala1396=) | |
2 | g.151672482C>G | CA348816610 | NEB | c.4186G>C (p.Ala1396Pro) | |
2 | g.151672482C>T | CA348816611 | NEB | c.4186G>A (p.Ala1396Thr) | |
2 | g.151672483C>A | CA348816612 | NEB | c.4185G>T (p.Met1395Ile) | |
2 | g.151672483C= | CA1298291165 | NEB | c.4185G= (p.Met1395=) | |
2 | g.151672483C>G | CA348816613 | NEB | c.4185G>C (p.Met1395Ile) | |
2 | g.151672483C>T | CA57651061 | NEB | c.4185G>A (p.Met1395Ile) | ClinVar dbSNP gnomAD v4 |
2 | g.151672484A>C | CA348816614 | NEB | c.4184T>G (p.Met1395Arg) |