| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000287934 |
| Start |
91266649:91266649(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1769C>T |
| AA Mutation |
p.Ala590Val(p.A590V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000287934 |
| Start |
91266711:91266711(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1831C>A |
| AA Mutation |
p.Leu611Met(p.L611M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
6 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000287934 |
| Start |
91265285:91265285(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.405C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |