| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000320895 |
| Start |
1338922:1338922(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.537G>A |
| AA Mutation |
p.Met179Ile(p.M179I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000320895 |
| Start |
1330348:1330348(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1012C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000320895 |
| Start |
1341788:1341788(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs762040634
|
| CDS Mutation |
c.336C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |