| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000397625 |
| Start |
76718826:76718826(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs537527655
|
| CDS Mutation |
c.1115A>G |
| AA Mutation |
p.His372Arg(p.H372R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000397625 |
| Start |
76718786:76718786(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs372217669
|
| CDS Mutation |
c.1155C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000397625 |
| Start |
76723887:76723887(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs778506056
|
| CDS Mutation |
c.690C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |