Gene >> CLDN17
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000286808 |
| Start |
30166172:30166172(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.446A>G |
| AA Mutation |
p.Tyr149Cys(p.Y149C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000286808 |
| Start |
30166516:30166516(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.102T>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |