| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000257915 |
| Start |
51172366:51172366(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.57G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000257915 |
| Start |
51098779:51098779(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1416T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
stop_gained;splice_region_variant |
| Transcription ID |
ENST00000257915 |
| Start |
51118621:51118621(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.274G>T |
| AA Mutation |
p.Gly92Ter(p.G92*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |