| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000228682 |
| Start |
57466250:57466250(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.773G>A |
| AA Mutation |
p.Ser258Asn(p.S258N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000228682 |
| Start |
57465153:57465153(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.432G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000228682 |
| Start |
57471068:57471068(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2328C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |