| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000252252 |
| Start |
52451576:52451576(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.503A>G |
| AA Mutation |
p.Lys168Arg(p.K168R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000252252 |
| Start |
52451638:52451638(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.441C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000252252 |
| Start |
52450525:52450525(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs143150216
|
| CDS Mutation |
c.636G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |