| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000356554 |
| Start |
117402226:117402226(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.343C>T |
| AA Mutation |
p.His115Tyr(p.H115Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000356554 |
| Start |
117493233:117493233(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1255G>T |
| AA Mutation |
p.Ala419Ser(p.A419S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000356554 |
| Start |
117522912:117522912(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs757179136
|
| CDS Mutation |
c.1881A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |