| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000302014 |
| Start |
140632190:140632190(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.794T>G |
| AA Mutation |
p.Val265Gly(p.V265G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000302014 |
| Start |
140632438:140632438(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.546G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000302014 |
| Start |
140632276:140632276(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs772768479
|
| CDS Mutation |
c.708G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |