| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000268919 |
| Start |
53824378:53824378(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1345G>T |
| AA Mutation |
p.Ala449Ser(p.A449S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000268919 |
| Start |
53824029:53824029(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.996G>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000268919 |
| Start |
53823861:53823861(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.828C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |