| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000354728 |
| Start |
233672602:233672602(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.668T>A |
| AA Mutation |
p.Phe223Tyr(p.F223Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000354728 |
| Start |
233672600:233672600(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.666T>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000354728 |
| Start |
233672102:233672102(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.168T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |