Gene >> ABCG2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000237612 |
| Start |
88118205:88118205(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.745A>G |
| AA Mutation |
p.Ile249Val(p.I249V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000237612 |
| Start |
88118216:88118216(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs766790636
|
| CDS Mutation |
c.734C>G |
| AA Mutation |
p.Pro245Arg(p.P245R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |