| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000318602 |
| Start |
9099431:9099431(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1651G>A |
| AA Mutation |
p.Val551Met(p.V551M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000318602 |
| Start |
9072863:9072863(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3765G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000318602 |
| Start |
9091228:9091228(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2442C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |