| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000315050 |
| Start |
151030723:151030723(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1901G>C |
| AA Mutation |
p.Gly634Ala(p.G634A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000315050 |
| Start |
151063668:151063668(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.216G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000315050 |
| Start |
151032309:151032309(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1854C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |