| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361247 |
| Start |
155961678:155961678(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1451C>A |
| AA Mutation |
p.Ala484Glu(p.A484E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361247 |
| Start |
155952718:155952718(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1894G>A |
| AA Mutation |
p.Ala632Thr(p.A632T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361247 |
| Start |
155961858:155961858(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1271A>T |
| AA Mutation |
p.Glu424Val(p.E424V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |