| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265441 |
| Start |
117320731:117320731(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.146G>T |
| AA Mutation |
p.Ser49Ile(p.S49I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000265441 |
| Start |
117320722:117320722(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.155G>A |
| AA Mutation |
p.Arg52Gln(p.R52Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000265441 |
| Start |
117297841:117297841(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.624C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |