| ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000350908 |
| Start |
114629915:114629915(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs751847176
|
| CDS Mutation |
c.507G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000350908 |
| Start |
114642522:114642522(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.888C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000350908 |
| Start |
114658225:114658225(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1426C>T |
| AA Mutation |
p.Arg476Ter(p.R476*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |