Gene >> SLC6A4
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261707 |
| Start |
30210562:30210562(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1402G>T |
| AA Mutation |
p.Ala468Ser(p.A468S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261707 |
| Start |
30211356:30211356(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs28914832
|
| CDS Mutation |
c.1273A>G |
| AA Mutation |
p.Ile425Val(p.I425V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |