| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000318607 |
| Start |
100706679:100706679(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1574A>G |
| AA Mutation |
p.Asn525Ser(p.N525S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000318607 |
| Start |
100721485:100721485(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.99G>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000318607 |
| Start |
100709600:100709600(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1104T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |