| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000450454 |
| Start |
23387331:23387331(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.908C>G |
| AA Mutation |
p.Thr303Ser(p.T303S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000450454 |
| Start |
23387332:23387332(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.907A>G |
| AA Mutation |
p.Thr303Ala(p.T303A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000450454 |
| Start |
23397847:23397847(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.552G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |