| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000344743 |
| Start |
58709999:58709999(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.658G>A |
| AA Mutation |
p.Asp220Asn(p.D220N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000344743 |
| Start |
58709955:58709955(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.702G>C |
| AA Mutation |
p.Leu234Phe(p.L234F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000344743 |
| Start |
58724482:58724482(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.15G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |