| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000393716 |
| Start |
119811558:119811558(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs576229324
|
| CDS Mutation |
c.351C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000393716 |
| Start |
119811702:119811702(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.495C>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000393716 |
| Start |
119811622:119811622(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.415G>T |
| AA Mutation |
p.Gly139Ter(p.G139*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |