| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000085219 |
| Start |
35332870:35332870(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.358A>T |
| AA Mutation |
p.Arg120Trp(p.R120W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000085219 |
| Start |
35332678:35332678(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.166T>C |
| AA Mutation |
p.Phe56Leu(p.F56L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000085219 |
| Start |
35341134:35341134(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1503C>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |