Gene >> BCAT1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261192 |
| Start |
24836530:24836530(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.884T>C |
| AA Mutation |
p.Leu295Pro(p.L295P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261192 |
| Start |
24849927:24849927(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.533C>A |
| AA Mutation |
p.Pro178His(p.P178H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |