Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.154580323_154590216del | CA915940499 | |||
4 | g.154589501del | CA3115394 | FGA | c.117del (p.Val40TrpfsTer?) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.154589501A= | CA1504945111 | FGA | c.116T= (p.Val39=) | |
4 | g.154589501A>C | CA358533863 | FGA | c.116T>G (p.Val39Gly) | |
4 | g.154589501A>G | CA358533865 | FGA | c.116T>C (p.Val39Ala) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.154589501A>T | CA126502 | FGA | c.116T>A (p.Val39Asp) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
4 | g.154589502C>A | CA358533868 | FGA | c.115G>T (p.Val39Phe) | COSMIC COSMIC |
4 | g.154589502C= | CA1504945112 | FGA | c.115G= (p.Val39=) | |
4 | g.154589502C>G | CA358533870 | FGA | c.115G>C (p.Val39Leu) | |
4 | g.154589502C>T | CA108763414 | FGA | c.115G>A (p.Val39Ile) | dbSNP |
4 | g.154589503C>A | CA358533874 | FGA | c.114G>T (p.Arg38Ser) | |
4 | g.154589503C= | CA1504945113 | FGA | c.114G= (p.Arg38=) | |
4 | g.154589503C>G | CA358533872 | FGA | c.114G>C (p.Arg38Ser) | ClinVar dbSNP |
4 | g.154589503C>T | CA441815573 | FGA | c.114G>A (p.Arg38=) | |
4 | g.154589504C>A | CA358533876 | FGA | c.113G>T (p.Arg38Met) | |
4 | g.154589504C>G | CA358533878 | FGA | c.113G>C (p.Arg38Thr) | |
4 | g.154589504C>T | CA358533880 | FGA | c.113G>A (p.Arg38Lys) | COSMIC COSMIC |
4 | g.154589505T>A | CA358533881 | FGA | c.112A>T (p.Arg38Trp) | |
4 | g.154589505T>C | CA126469 | FGA | c.112A>G (p.Arg38Gly) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.154589505T>G | CA441815574 | FGA | c.112A>C (p.Arg38=) | |
4 | g.154589505T= | CA1504945114 | FGA | c.112A= (p.Arg38=) | |
4 | g.154589506T>A | CA441815575 | FGA | c.111A>T (p.Pro37=) | |
4 | g.154589506T>C | CA441815576 | FGA | c.111A>G (p.Pro37=) | |
4 | g.154589506T>G | CA441815577 | FGA | c.111A>C (p.Pro37=) | |
4 | g.154589507G>A | CA126474 | FGA | c.110C>T (p.Pro37Leu) | ClinVar dbSNP |
4 | g.154589507G>C | CA358533886 | FGA | c.110C>G (p.Pro37Arg) | |
4 | g.154589507G= | CA1504945115 | FGA | c.110C= (p.Pro37=) | |
4 | g.154589507G>T | CA358533885 | FGA | c.110C>A (p.Pro37Gln) | |
4 | g.154589508G>A | CA358533890 | FGA | c.109C>T (p.Pro37Ser) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.154589508G>C | CA358533891 | FGA | c.109C>G (p.Pro37Ala) | |
4 | g.154589508G= | CA1504945116 | FGA | c.109C= (p.Pro37=) | |
4 | g.154589508G>T | CA358533893 | FGA | c.109C>A (p.Pro37Thr) | |
4 | g.154589509G>A | CA441815578 | FGA | c.108C>T (p.Gly36=) | |
4 | g.154589509G>C | CA441815579 | FGA | c.108C>G (p.Gly36=) | |
4 | g.154589509G= | CA1504945117 | FGA | c.108C= (p.Gly36=) | |
4 | g.154589509G>T | CA441815580 | FGA | c.108C>A (p.Gly36=) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.154589510C>A | CA358533895 | FGA | c.107G>T (p.Gly36Val) | COSMIC COSMIC COSMIC |
4 | g.154589510C>G | CA358533897 | FGA | c.107G>C (p.Gly36Ala) | |
4 | g.154589510C>T | CA358533899 | FGA | c.107G>A (p.Gly36Asp) | ClinVar gnomAD v4 |
4 | g.154589511C>A | CA358533903 | FGA | c.106G>T (p.Gly36Cys) | |
4 | g.154589511C>G | CA358533901 | FGA | c.106G>C (p.Gly36Arg) | |
4 | g.154589511C>T | CA358533902 | FGA | c.106G>A (p.Gly36Ser) | |
4 | g.154589512A>C | CA441815581 | FGA | c.105T>G (p.Arg35=) | |
4 | g.154589512A>G | CA441815582 | FGA | c.105T>C (p.Arg35=) | |
4 | g.154589512A>T | CA441815583 | FGA | c.105T>A (p.Arg35=) | |
4 | g.154589513C>A | CA358533904 | FGA | c.104G>T (p.Arg35Leu) | |
4 | g.154589513C= | CA1504945118 | FGA | c.104G= (p.Arg35=) | |
4 | g.154589513C>G | CA358533905 | FGA | c.104G>C (p.Arg35Pro) | ClinVar dbSNP |
4 | g.154589513C>T | CA130224 | FGA | c.104G>A (p.Arg35His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
4 | g.154589513_154589514delinsTT | CA2580616796 | FGA | c.103_104delinsAA (p.Arg35Asn) | ClinVar |