| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000302909 |
| Start |
26727831:26727831(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs773900452
|
| CDS Mutation |
c.448C>T |
| AA Mutation |
p.Arg150Trp(p.R150W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000302909 |
| Start |
26728030:26728030(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.647C>T |
| AA Mutation |
p.Thr216Met(p.T216M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000302909 |
| Start |
26728433:26728433(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1050C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |