| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000393775 |
| Start |
118930181:118930181(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs746094445
|
| CDS Mutation |
c.147C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000393775 |
| Start |
118928642:118928642(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.291C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000393775 |
| Start |
118930178:118930178(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.150T>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |