| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264162 |
| Start |
135822069:135822069(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.937G>A |
| AA Mutation |
p.Gly313Arg(p.G313R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264162 |
| Start |
135809466:135809466(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2881G>A |
| AA Mutation |
p.Ala961Thr(p.A961T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000264162 |
| Start |
135809440:135809440(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2907G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |