| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000359451 |
| Start |
110108649:110108649(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.301T>G |
| AA Mutation |
p.Phe101Val(p.F101V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000359451 |
| Start |
110108574:110108574(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.376G>A |
| AA Mutation |
p.Asp126Asn(p.D126N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000359451 |
| Start |
110107119:110107119(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs758077376
|
| CDS Mutation |
c.498G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |