| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000356577 |
| Start |
33549781:33549781(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.550G>T |
| AA Mutation |
p.Ala184Ser(p.A184S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000356577 |
| Start |
33552818:33552818(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3587C>T |
| AA Mutation |
p.Pro1196Leu(p.P1196L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000356577 |
| Start |
33550758:33550758(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1527G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |