| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000302759 |
| Start |
110642168:110642168(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2414C>T |
| AA Mutation |
p.Thr805Ile(p.T805I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000302759 |
| Start |
110641139:110641139(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2850T>A |
| AA Mutation |
p.Ser950Arg(p.S950R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000302759 |
| Start |
110658663:110658663(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1356G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |