| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000371946 |
| Start |
46558769:46558769(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs774831453
|
| CDS Mutation |
c.1204G>A |
| AA Mutation |
p.Ala402Thr(p.A402T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000371946 |
| Start |
46580601:46580601(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.163C>T |
| AA Mutation |
p.Leu55Phe(p.L55F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000371946 |
| Start |
46565098:46565098(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.711T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |