| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000281043 |
| Start |
15942098:15942098(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.34A>G |
| AA Mutation |
p.Met12Val(p.M12V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000281043 |
| Start |
15942363:15942363(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.299G>T |
| AA Mutation |
p.Gly100Val(p.G100V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000281043 |
| Start |
15942583:15942583(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.519C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |