| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000281171 |
| Start |
15503938:15503938(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1136A>G |
| AA Mutation |
p.Glu379Gly(p.E379G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000281171 |
| Start |
15595003:15595003(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3613A>T |
| AA Mutation |
p.Ile1205Phe(p.I1205F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000281171 |
| Start |
15549204:15549204(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs147165417
|
| CDS Mutation |
c.2415G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |