| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000366577 |
| Start |
236895430:236895430(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3478G>A |
| AA Mutation |
p.Val1160Ile(p.V1160I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000366577 |
| Start |
236795722:236795722(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.19G>T |
| AA Mutation |
p.Asp7Tyr(p.D7Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000366577 |
| Start |
236889204:236889204(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2875C>G |
| AA Mutation |
p.Gln959Glu(p.Q959E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |