| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264708 |
| Start |
25161559:25161559(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.326C>T |
| AA Mutation |
p.Ala109Val(p.A109V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000264708 |
| Start |
25161204:25161204(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.681C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000264708 |
| Start |
25161309:25161309(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs767274513
|
| CDS Mutation |
c.576C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |