| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000253144 |
| Start |
53571656:53571656(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.62C>T |
| AA Mutation |
p.Ala21Val(p.A21V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000253144 |
| Start |
53571693:53571693(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs757867528
|
| CDS Mutation |
c.99C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000253144 |
| Start |
53577289:53577289(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs569571621
|
| CDS Mutation |
c.729C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |