Gene >> AMELX
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000380714 |
| Start |
11298746:11298746(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs760321133
|
| CDS Mutation |
c.343C>T |
| AA Mutation |
p.His115Tyr(p.H115Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000380714 |
| Start |
11298702:11298702(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.299T>G |
| AA Mutation |
p.Met100Arg(p.M100R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |