| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000333360 |
| Start |
169732959:169732959(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.77C>A |
| AA Mutation |
p.Thr26Asn(p.T26N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000333360 |
| Start |
169731839:169731839(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.525G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000333360 |
| Start |
169727788:169727788(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs761064301
|
| CDS Mutation |
c.1419T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |