| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000344626 |
| Start |
11059800:11059800(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4683G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
7 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000344626 |
| Start |
11059833:11059833(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4716C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
8 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000344626 |
| Start |
11023590:11023590(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2932C>T |
| AA Mutation |
p.Arg978Ter(p.R978*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |