| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000253801 |
| Start |
42904023:42904023(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.323C>T |
| AA Mutation |
p.Thr108Ile(p.T108I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000253801 |
| Start |
42907536:42907536(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs766771010
|
| CDS Mutation |
c.354C>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000253801 |
| Start |
42911240:42911240(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.888C>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |