| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368919 |
| Start |
110442645:110442645(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.782G>T |
| AA Mutation |
p.Gly261Val(p.G261V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368919 |
| Start |
110431252:110431252(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1440C>A |
| AA Mutation |
p.Ser480Arg(p.S480R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000368919 |
| Start |
110442461:110442461(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.966G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |