| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000382285 |
| Start |
353324:353324(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.304G>A |
| AA Mutation |
p.Asp102Asn(p.D102N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000382285 |
| Start |
349682:349682(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs368963058
|
| CDS Mutation |
c.39C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000382285 |
| Start |
353335:353335(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.315A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |