| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000239165 |
| Start |
48610592:48610592(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.327C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000239165 |
| Start |
48610568:48610568(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs2228185
|
| CDS Mutation |
c.351C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000239165 |
| Start |
48610673:48610673(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.246G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |