| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000244289 |
| Start |
42406266:42406266(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2260C>G |
| AA Mutation |
p.Pro754Ala(p.P754A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000244289 |
| Start |
42405419:42405419(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2508G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000244289 |
| Start |
42410649:42410649(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1077G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |