| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000237837 |
| Start |
4379382:4379382(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.201G>T |
| AA Mutation |
p.Gln67His(p.Q67H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000237837 |
| Start |
4370733:4370733(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs145147639
|
| CDS Mutation |
c.366C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000237837 |
| Start |
4370742:4370742(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.357G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |