| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000367651 |
| Start |
139373651:139373651(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.294C>A |
| AA Mutation |
p.Phe98Leu(p.F98L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000367651 |
| Start |
139373538:139373538(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.407C>A |
| AA Mutation |
p.Pro136Gln(p.P136Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000367651 |
| Start |
139373537:139373537(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.408G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |