| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000270861 |
| Start |
127895084:127895084(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2694G>C |
| AA Mutation |
p.Trp898Cys(p.W898C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000270861 |
| Start |
127883519:127883519(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.303A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000270861 |
| Start |
127893878:127893878(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2559C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |