| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000310624 |
| Start |
29485820:29485820(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs752243905
|
| CDS Mutation |
c.1181C>T |
| AA Mutation |
p.Ala394Val(p.A394V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000310624 |
| Start |
29490661:29490661(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3021T>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000310624 |
| Start |
29490328:29490328(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2688G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |