| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.94762804del | CA2610262556 | CYP2C19 | c.99del (p.Thr34LeufsTer5) c.932-12254del (n.932-12254del) | gnomAD v4 |
| 10 | g.94762803_94762804delinsCC | CA1929213819 | CYP2C19 | c.98_99delinsCC (p.Pro33=) c.932-12255_932-12254delinsCC (n.932-12255_932-12254delinsCC) | |
| 10 | g.94762804C>A | CA2580977569 | CYP2C19 | c.99C>A (p.Pro33=) c.932-12254C>A (n.932-12254C>A) | |
| 10 | g.94762804C= | CA5616303 | CYP2C19 | c.99C= (p.Pro33=) c.932-12254C= (n.932-12254C=) | |
| 10 | g.94762804C>G | CA2580977568 | CYP2C19 | c.99C>G (p.Pro33=) c.932-12254C>G (n.932-12254C>G) | |
| 10 | g.94762804C>T | CA211666534 | CYP2C19 | c.99C>T (p.Pro33=) c.932-12254C>T (n.932-12254C>T) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.94762804delinsTACCCT | CA918736410 | CYP2C19 | c.99delinsTACCCT (p.Pro35LeufsTer6) c.932-12254delinsTACCCT (n.932-12254delinsTACCCT) | dbSNP |
| 10 | g.94762804_94762805insCCT | CA931367494 | CYP2C19 | c.99_100insCCT (p.Pro33_Thr34insPro) c.932-12254_932-12253insCCT (n.932-12254_932-12253insCCT) | dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.94762805A>C | CA377668081 | CYP2C19 | c.100A>C (p.Thr34Pro) c.932-12253A>C (n.932-12253A>C) | |
| 10 | g.94762805A>G | CA377668083 | CYP2C19 | c.100A>G (p.Thr34Ala) c.932-12253A>G (n.932-12253A>G) | |
| 10 | g.94762805A>T | CA377668085 | CYP2C19 | c.100A>T (p.Thr34Ser) c.932-12253A>T (n.932-12253A>T) | |
| 10 | g.94762806_94762807insCCTAC | CA2695212479 | CYP2C19 | c.101_102insCCTAC (p.Pro35LeufsTer6) c.932-12252_932-12251insCCTAC (n.932-12252_932-12251insCCTAC) | |
| 10 | g.94762805_94762806insGGAGGGAGTT | CA2610262565 | CYP2C19 | c.100_101insGGAGGGAGTT (p.Thr34ArgfsTer18) c.932-12253_932-12252insGGAGGGAGTT (n.932-12253_932-12252insGGAGGGAGTT) | gnomAD v4 |
| 10 | g.94762806C>A | CA377668087 | CYP2C19 | c.101C>A (p.Thr34Asn) c.932-12252C>A (n.932-12252C>A) | gnomAD v4 |
| 10 | g.94762806C= | CA1929213832 | CYP2C19 | c.101C= (p.Thr34=) c.932-12252C= (n.932-12252C=) | |
| 10 | g.94762806C>G | CA377668088 | CYP2C19 | c.101C>G (p.Thr34Ser) c.932-12252C>G (n.932-12252C>G) | |
| 10 | g.94762806C>T | CA377668090 | CYP2C19 | c.101C>T (p.Thr34Ile) c.932-12252C>T (n.932-12252C>T) | dbSNP gnomAD v4 |
| 10 | g.94762807T>A | CA470824229 | CYP2C19 | c.102T>A (p.Thr34=) c.932-12251T>A (n.932-12251T>A) | |
| 10 | g.94762807T>C | CA470824230 | CYP2C19 | c.102T>C (p.Thr34=) c.932-12251T>C (n.932-12251T>C) | gnomAD v4 |
| 10 | g.94762807T>G | CA470824231 | CYP2C19 | c.102T>G (p.Thr34=) c.932-12251T>G (n.932-12251T>G) | |
| 10 | g.94762808C>A | CA377668092 | CYP2C19 | c.103C>A (p.Pro35Thr) c.932-12250C>A (n.932-12250C>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.94762808C= | CA1929213837 | CYP2C19 | c.103C= (p.Pro35=) c.932-12250C= (n.932-12250C=) | |
| 10 | g.94762808C>G | CA377668094 | CYP2C19 | c.103C>G (p.Pro35Ala) c.932-12250C>G (n.932-12250C>G) | |
| 10 | g.94762808C>T | CA377668095 | CYP2C19 | c.103C>T (p.Pro35Ser) c.932-12250C>T (n.932-12250C>T) | dbSNP gnomAD v4 |
| 10 | g.94762809C>A | CA377668099 | CYP2C19 | c.104C>A (p.Pro35His) c.932-12249C>A (n.932-12249C>A) | |
| 10 | g.94762809C>G | CA377668100 | CYP2C19 | c.104C>G (p.Pro35Arg) c.932-12249C>G (n.932-12249C>G) | |
| 10 | g.94762809C>T | CA377668097 | CYP2C19 | c.104C>T (p.Pro35Leu) c.932-12249C>T (n.932-12249C>T) | COSMIC |
| 10 | g.94762810T>A | CA470824232 | CYP2C19 | c.105T>A (p.Pro35=) c.932-12248T>A (n.932-12248T>A) | |
| 10 | g.94762810T>C | CA470824233 | CYP2C19 | c.105T>C (p.Pro35=) c.932-12248T>C (n.932-12248T>C) | |
| 10 | g.94762810T>G | CA470824234 | CYP2C19 | c.105T>G (p.Pro35=) c.932-12248T>G (n.932-12248T>G) | |
| 10 | g.94762811C>A | CA377668103 | CYP2C19 | c.106C>A (p.Leu36Ile) c.932-12247C>A (n.932-12247C>A) | |
| 10 | g.94762811C= | CA1929213844 | CYP2C19 | c.106C= (p.Leu36=) c.932-12247C= (n.932-12247C=) | |
| 10 | g.94762811C>G | CA377668104 | CYP2C19 | c.106C>G (p.Leu36Val) c.932-12247C>G (n.932-12247C>G) | |
| 10 | g.94762811C>T | CA377668106 | CYP2C19 | c.106C>T (p.Leu36Phe) c.932-12247C>T (n.932-12247C>T) | dbSNP COSMIC |
| 10 | g.94762812T>A | CA377668109 | CYP2C19 | c.107T>A (p.Leu36His) c.932-12246T>A (n.932-12246T>A) | |
| 10 | g.94762812T>C | CA377668111 | CYP2C19 | c.107T>C (p.Leu36Pro) c.932-12246T>C (n.932-12246T>C) | |
| 10 | g.94762812T>G | CA377668112 | CYP2C19 | c.107T>G (p.Leu36Arg) c.932-12246T>G (n.932-12246T>G) | dbSNP |
| 10 | g.94762812T= | CA1929213847 | CYP2C19 | c.107T= (p.Leu36=) c.932-12246T= (n.932-12246T=) | |
| 10 | g.94762813C>A | CA470824235 | CYP2C19 | c.108C>A (p.Leu36=) c.932-12245C>A (n.932-12245C>A) | |
| 10 | g.94762813C>G | CA470824236 | CYP2C19 | c.108C>G (p.Leu36=) c.932-12245C>G (n.932-12245C>G) | |
| 10 | g.94762813C>T | CA470824237 | CYP2C19 | c.108C>T (p.Leu36=) c.932-12245C>T (n.932-12245C>T) | |
| 10 | g.94762814C>A | CA377668118 | CYP2C19 | c.109C>A (p.Pro37Thr) c.932-12244C>A (n.932-12244C>A) | |
| 10 | g.94762814C>G | CA377668119 | CYP2C19 | c.109C>G (p.Pro37Ala) c.932-12244C>G (n.932-12244C>G) | |
| 10 | g.94762814C>T | CA377668122 | CYP2C19 | c.109C>T (p.Pro37Ser) c.932-12244C>T (n.932-12244C>T) | gnomAD v4 |
| 10 | g.94762815C>A | CA377668124 | CYP2C19 | c.110C>A (p.Pro37Gln) c.932-12243C>A (n.932-12243C>A) | |
| 10 | g.94762815C>G | CA377668126 | CYP2C19 | c.110C>G (p.Pro37Arg) c.932-12243C>G (n.932-12243C>G) | |
| 10 | g.94762815C>T | CA377668127 | CYP2C19 | c.110C>T (p.Pro37Leu) c.932-12243C>T (n.932-12243C>T) | |
| 10 | g.94762816A= | CA1929213851 | CYP2C19 | c.111A= (p.Pro37=) c.932-12242A= (n.932-12242A=) | |
| 10 | g.94762816A>C | CA470824245 | CYP2C19 | c.111A>C (p.Pro37=) c.932-12242A>C (n.932-12242A>C) | gnomAD v4 |
| 10 | g.94762816A>G | CA470824247 | CYP2C19 | c.111A>G (p.Pro37=) c.932-12242A>G (n.932-12242A>G) | dbSNP gnomAD v2 |