Gene >> CNTNAP1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264638 |
| Start |
42685303:42685303(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.598G>A |
| AA Mutation |
p.Ala200Thr(p.A200T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000264638 |
| Start |
42685380:42685380(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.675C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |