Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.49459142_49459160del | CA2695206696 | MMUT | c.309_327del (p.Arg103SerfsTer?) | |
6 | g.49459148_49459149delinsTG | CA1627396617 | MMUT | c.318_319delinsCA (p.Thr106=) | |
6 | g.49459149G>A | CA450609505 | MMUT | c.318C>T (p.Thr106=) | gnomAD v4 |
6 | g.49459149G>C | CA450609506 | MMUT | c.318C>G (p.Thr106=) | |
6 | g.49459149G>T | CA450609507 | MMUT | c.318C>A (p.Thr106=) | |
6 | g.49459150del | CA825483786 | MMUT | c.318del (p.Ile107SerfsTer?) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.49459150G>A | CA364405010 | MMUT | c.317C>T (p.Thr106Ile) | ClinVar dbSNP |
6 | g.49459150G>C | CA364405009 | MMUT | c.317C>G (p.Thr106Ser) | |
6 | g.49459150G= | CA1627396628 | MMUT | c.317C= (p.Thr106=) | |
6 | g.49459150G>T | CA364405008 | MMUT | c.317C>A (p.Thr106Asn) | |
6 | g.49459151T>A | CA364405011 | MMUT | c.316A>T (p.Thr106Ser) | |
6 | g.49459151T>C | CA364405012 | MMUT | c.316A>G (p.Thr106Ala) | |
6 | g.49459151T>G | CA364405013 | MMUT | c.316A>C (p.Thr106Pro) | |
6 | g.49459152C>A | CA364405014 | MMUT | c.315G>T (p.Trp105Cys) | |
6 | g.49459152C>G | CA364405015 | MMUT | c.315G>C (p.Trp105Cys) | |
6 | g.49459152C>T | CA364405016 | MMUT | c.315G>A (p.Trp105Ter) | gnomAD v4 |
6 | g.49459153C>A | CA364405017 | MMUT | c.314G>T (p.Trp105Leu) | gnomAD v4 |
6 | g.49459153C>G | CA364405019 | MMUT | c.314G>C (p.Trp105Ser) | |
6 | g.49459153C>T | CA364405018 | MMUT | c.314G>A (p.Trp105Ter) | |
6 | g.49459154A= | CA1627396630 | MMUT | c.313T= (p.Trp105=) | |
6 | g.49459154A>C | CA364405020 | MMUT | c.313T>G (p.Trp105Gly) | |
6 | g.49459154A>G | CA249727 | MMUT | c.313T>C (p.Trp105Arg) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49459154A>T | CA364405021 | MMUT | c.313T>A (p.Trp105Arg) | |
6 | g.49459154_49459155delinsAG | CA1627396633 | MMUT | c.312_313delinsCT (p.Pro104=) | |
6 | g.49459155G>A | CA450609511 | MMUT | c.312C>T (p.Pro104=) | gnomAD v4 |
6 | g.49459155G>C | CA450609512 | MMUT | c.312C>G (p.Pro104=) | gnomAD v4 |
6 | g.49459155G>T | CA450609513 | MMUT | c.312C>A (p.Pro104=) | |
6 | g.49459157del | CA16618295 | MMUT | c.312del (p.Trp105GlyfsTer?) | ClinVar dbSNP gnomAD v4 |
6 | g.49459156G>A | CA364405022 | MMUT | c.311C>T (p.Pro104Leu) | COSMIC |
6 | g.49459156G>C | CA364405023 | MMUT | c.311C>G (p.Pro104Arg) | |
6 | g.49459156G>T | CA364405024 | MMUT | c.311C>A (p.Pro104His) | |
6 | g.49459157G>A | CA3847139 | MMUT | c.310C>T (p.Pro104Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49459157G>C | CA364405025 | MMUT | c.310C>G (p.Pro104Ala) | |
6 | g.49459157G= | CA1627396650 | MMUT | c.310C= (p.Pro104=) | |
6 | g.49459157G>T | CA364405026 | MMUT | c.310C>A (p.Pro104Thr) | |
6 | g.49459158C>A | CA364405027 | MMUT | c.309G>T (p.Arg103Ser) | gnomAD v4 |
6 | g.49459158C>G | CA364405028 | MMUT | c.309G>C (p.Arg103Ser) | |
6 | g.49459158C>T | CA450609517 | MMUT | c.309G>A (p.Arg103=) | gnomAD v4 |
6 | g.49459159C>A | CA364405031 | MMUT | c.308G>T (p.Arg103Met) | |
6 | g.49459159C>G | CA364405030 | MMUT | c.308G>C (p.Arg103Thr) | |
6 | g.49459159C>T | CA364405029 | MMUT | c.308G>A (p.Arg103Lys) | |
6 | g.49459159_49459160insGCACCGCG | CA2550235074 | MMUT | c.307_308insCGCGGTGC (p.Arg103ThrfsTer?) | |
6 | g.49459160T>A | CA364405032 | MMUT | c.307A>T (p.Arg103Trp) | |
6 | g.49459160T>C | CA364405033 | MMUT | c.307A>G (p.Arg103Gly) | |
6 | g.49459160T>G | CA450609521 | MMUT | c.307A>C (p.Arg103=) | |
6 | g.49459161A>C | CA364405034 | MMUT | c.306T>G (p.Phe102Leu) | |
6 | g.49459161A>G | CA450609522 | MMUT | c.306T>C (p.Phe102=) | gnomAD v4 |
6 | g.49459161A>T | CA364405035 | MMUT | c.306T>A (p.Phe102Leu) | |
6 | g.49459161_49459162insCATGGTGGCCTGCGGGCCGCGC | CA2544888496 | MMUT | c.305_306insGCGCGGCCCGCAGGCCACCATG (p.Phe102LeufsTer9) | |
6 | g.49459162A>C | CA364405036 | MMUT | c.305T>G (p.Phe102Cys) |