| ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000285979 |
| Start |
94724422:94724422(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1038C>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000285979 |
| Start |
94720497:94720497(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.921A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000285979 |
| Start |
94688153:94688153(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.360G>A |
| AA Mutation |
p.Trp120Ter(p.W120*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |