| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256442 |
| Start |
69175026:69175026(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.855G>A |
| AA Mutation |
p.Met285Ile(p.M285I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256442 |
| Start |
69171387:69171387(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.481G>A |
| AA Mutation |
p.Gly161Arg(p.G161R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000256442 |
| Start |
69175426:69175426(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.972A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |