| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000354373 |
| Start |
29438835:29438835(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.44A>G |
| AA Mutation |
p.His15Arg(p.H15R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000354373 |
| Start |
29441607:29441607(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs750004982
|
| CDS Mutation |
c.439G>A |
| AA Mutation |
p.Val147Ile(p.V147I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000354373 |
| Start |
29441933:29441933(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs761611163
|
| CDS Mutation |
c.765C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |