Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.49459142_49459160del | CA2695206696 | MMUT | c.309_327del (p.Arg103SerfsTer?) | |
6 | g.49459144_49459145delinsCG | CA1627396587 | MMUT | c.322_323delinsCG (p.Arg108=) | |
6 | g.49459145G>A | CA249732 | MMUT | c.322C>T (p.Arg108Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49459145G>C | CA364404999 | MMUT | c.322C>G (p.Arg108Gly) | ClinVar dbSNP gnomAD v4 |
6 | g.49459145G= | CA1627396604 | MMUT | c.322C= (p.Arg108=) | |
6 | g.49459145G>T | CA364405000 | MMUT | c.322C>A (p.Arg108Ser) | |
6 | g.49459146del | CA566931455 | MMUT | c.322del (p.Arg108AlafsTer?) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49459146G>A | CA3847138 | MMUT | c.321C>T (p.Ile107=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
6 | g.49459146G>C | CA364405001 | MMUT | c.321C>G (p.Ile107Met) | |
6 | g.49459146G= | CA1627396613 | MMUT | c.321C= (p.Ile107=) | |
6 | g.49459146G>T | CA450399754 | MMUT | c.321C>A (p.Ile107=) | dbSNP |
6 | g.49459147A>C | CA364405002 | MMUT | c.320T>G (p.Ile107Ser) | |
6 | g.49459147A>G | CA364405003 | MMUT | c.320T>C (p.Ile107Thr) | |
6 | g.49459147A>T | CA364405004 | MMUT | c.320T>A (p.Ile107Asn) | |
6 | g.49459148T>A | CA364405005 | MMUT | c.319A>T (p.Ile107Phe) | gnomAD v4 |
6 | g.49459148T>C | CA364405006 | MMUT | c.319A>G (p.Ile107Val) | gnomAD v4 |
6 | g.49459148T>G | CA364405007 | MMUT | c.319A>C (p.Ile107Leu) | |
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=) |