| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264956 |
| Start |
5753845:5753845(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs146028983
|
| CDS Mutation |
c.1376C>T |
| AA Mutation |
p.Thr459Met(p.T459M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000264956 |
| Start |
5797115:5797115(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs537471996
|
| CDS Mutation |
c.1980G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000264956 |
| Start |
5802036:5802036(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs202236029
|
| CDS Mutation |
c.2391C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |