| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000204615 |
| Start |
184375989:184375989(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.40C>G |
| AA Mutation |
p.Leu14Val(p.L14V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000204615 |
| Start |
184372707:184372707(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.868C>T |
| AA Mutation |
p.Pro290Ser(p.P290S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000204615 |
| Start |
184373466:184373466(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.345T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |