| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000380871 |
| Start |
23681289:23681289(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs769852677
|
| CDS Mutation |
c.637G>A |
| AA Mutation |
p.Val213Met(p.V213M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000380871 |
| Start |
23681287:23681287(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.639G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000380871 |
| Start |
23681383:23681383(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.543A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |