| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000205948 |
| Start |
66214485:66214485(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.950A>C |
| AA Mutation |
p.Asp317Ala(p.D317A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000205948 |
| Start |
66223735:66223735(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs762382292
|
| CDS Mutation |
c.378G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000205948 |
| Start |
66214529:66214529(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.906T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |