Gene >> ACCS
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263776 |
| Start |
44083736:44083736(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1450G>T |
| AA Mutation |
p.Val484Leu(p.V484L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263776 |
| Start |
44067766:44067766(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.139C>G |
| AA Mutation |
p.Leu47Val(p.L47V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |