| ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000612630 |
| Start |
4956789:4956789(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2211C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000612630 |
| Start |
4944148:4944148(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1090C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000612630 |
| Start |
4954389:4954389(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1858C>T |
| AA Mutation |
p.Arg620Ter(p.R620*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |