Gene >> SCML2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000251900 |
| Start |
18265698:18265698(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.835C>G |
| AA Mutation |
p.Gln279Glu(p.Q279E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000251900 |
| Start |
18258225:18258225(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1092T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |