Gene >> IAPP
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000240652 |
| Start |
21373379:21373379(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.28C>A |
| AA Mutation |
p.Leu10Ile(p.L10I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000240652 |
| Start |
21378334:21378334(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.178C>G |
| AA Mutation |
p.Leu60Val(p.L60V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |