| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256737 |
| Start |
26541959:26541959(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1045A>C |
| AA Mutation |
p.Ser349Arg(p.S349R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256737 |
| Start |
26547536:26547536(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1275T>A |
| AA Mutation |
p.Asn425Lys(p.N425K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000256737 |
| Start |
26598408:26598408(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs776129793
|
| CDS Mutation |
c.1491G>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |