Gene >> S100B
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000291700 |
| Start |
46602304:46602304(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.112A>G |
| AA Mutation |
p.Asn38Asp(p.N38D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000291700 |
| Start |
46599414:46599414(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.228C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |