| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000242159 |
| Start |
27155100:27155100(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.502T>G |
| AA Mutation |
p.Cys168Gly(p.C168G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000242159 |
| Start |
27156501:27156501(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.45G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000242159 |
| Start |
27156327:27156327(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.219C>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |