| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000367288 |
| Start |
201900547:201900547(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs369116037
|
| CDS Mutation |
c.466C>T |
| AA Mutation |
p.Arg156Trp(p.R156W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000367288 |
| Start |
201946230:201946230(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.111C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000367288 |
| Start |
201899954:201899954(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1059G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |