| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000370981 |
| Start |
68047234:68047234(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.64G>A |
| AA Mutation |
p.Ala22Thr(p.A22T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000370981 |
| Start |
68047013:68047013(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs763794708
|
| CDS Mutation |
c.285C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000370981 |
| Start |
68047181:68047181(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.117C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |