| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000369329 |
| Start |
90536396:90536396(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs774760752
|
| CDS Mutation |
c.1297G>A |
| AA Mutation |
p.Gly433Arg(p.G433R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000369329 |
| Start |
90536376:90536376(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1317C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000369329 |
| Start |
90556600:90556600(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.507A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |