| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000393955 |
| Start |
66871744:66871744(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs757830976
|
| CDS Mutation |
c.264C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000393955 |
| Start |
66851187:66851187(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2076G>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000393955 |
| Start |
66850911:66850911(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs757893864
|
| CDS Mutation |
c.2236C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |