| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000371708 |
| Start |
44229958:44229958(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.366G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000371708 |
| Start |
44230879:44230879(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs755679281
|
| CDS Mutation |
c.756C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000371708 |
| Start |
44231386:44231386(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.789A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |