| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000398988 |
| Start |
27609235:27609235(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1786G>T |
| AA Mutation |
p.Asp596Tyr(p.D596Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000398988 |
| Start |
27605754:27605754(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1590G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000398988 |
| Start |
27610106:27610106(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1920C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |