| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265992 |
| Start |
96058003:96058003(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs755283197
|
| CDS Mutation |
c.881C>T |
| AA Mutation |
p.Thr294Met(p.T294M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265992 |
| Start |
96056918:96056918(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs187113717
|
| CDS Mutation |
c.498C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265992 |
| Start |
96057224:96057224(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.684G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |