Gene >> AMY2A
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000414303 |
| Start |
103617597:103617597(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.157G>C |
| AA Mutation |
p.Gly53Arg(p.G53R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000414303 |
| Start |
103617576:103617576(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.136T>G |
| AA Mutation |
p.Tyr46Asp(p.Y46D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |