| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000216122 |
| Start |
35416713:35416713(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1489G>C |
| AA Mutation |
p.Glu497Gln(p.E497Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000216122 |
| Start |
35400497:35400497(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.59A>G |
| AA Mutation |
p.Gln20Arg(p.Q20R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000216122 |
| Start |
35406603:35406603(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.474C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |