| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000547270 |
| Start |
141973456:141973456(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.234T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000547270 |
| Start |
141973288:141973288(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.402C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000547270 |
| Start |
141973339:141973339(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.351C>G |
| AA Mutation |
p.Tyr117Ter(p.Y117*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |