| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368845 |
| Start |
124403806:124403806(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.763A>T |
| AA Mutation |
p.Arg255Trp(p.R255W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368845 |
| Start |
124400916:124400916(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1083G>A |
| AA Mutation |
p.Met361Ile(p.M361I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000368845 |
| Start |
124412124:124412124(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs143526711
|
| CDS Mutation |
c.48C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |