Gene >> GHRL
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000335542 |
| Start |
10289806:10289806(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.181G>A |
| AA Mutation |
p.Asp61Asn(p.D61N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000335542 |
| Start |
10286807:10286807(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs149447194
|
| CDS Mutation |
c.231C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |