| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000428726 |
| Start |
35229228:35229228(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2124A>T |
| AA Mutation |
p.Glu708Asp(p.E708D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000428726 |
| Start |
35196812:35196812(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.734T>G |
| AA Mutation |
p.Phe245Cys(p.F245C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000428726 |
| Start |
35206191:35206191(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1362C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |