| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000360803 |
| Start |
1007093:1007093(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1078C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000360803 |
| Start |
1009555:1009555(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1218A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000360803 |
| Start |
1012474:1012474(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1354G>T |
| AA Mutation |
p.Glu452Ter(p.E452*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |