Gene >> CHRM2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000320658 |
| Start |
137015034:137015034(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs143842239
|
| CDS Mutation |
c.169G>A |
| AA Mutation |
p.Val57Ile(p.V57I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000320658 |
| Start |
137015621:137015621(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs531986911
|
| CDS Mutation |
c.756C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |