| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000373344 |
| Start |
77523304:77523304(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.6797T>G |
| AA Mutation |
p.Leu2266Trp(p.L2266W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000373344 |
| Start |
77683318:77683318(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1938A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000373344 |
| Start |
77683732:77683732(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1524C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |