| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000254718 |
| Start |
4543048:4543048(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs769485013
|
| CDS Mutation |
c.2757C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000254718 |
| Start |
4539466:4539466(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.3936T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000254718 |
| Start |
4548205:4548205(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1662T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |