| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000341105 |
| Start |
128481173:128481173(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1289C>A |
| AA Mutation |
p.Ala430Glu(p.A430E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000341105 |
| Start |
128485866:128485866(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.732C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000341105 |
| Start |
128481130:128481130(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs770768777
|
| CDS Mutation |
c.1332G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |