| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000335288 |
| Start |
113652964:113652964(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs139958643
|
| CDS Mutation |
c.464C>T |
| AA Mutation |
p.Thr155Met(p.T155M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000335288 |
| Start |
113650420:113650420(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs370798858
|
| CDS Mutation |
c.700G>A |
| AA Mutation |
p.Gly234Arg(p.G234R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000335288 |
| Start |
113650490:113650490(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs199961422
|
| CDS Mutation |
c.630C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |