Gene >> BCAT1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261192 |
| Start |
24849861:24849861(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.599A>C |
| AA Mutation |
p.Asn200Thr(p.N200T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261192 |
| Start |
24878537:24878537(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.503G>A |
| AA Mutation |
p.Gly168Glu(p.G168E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |