Gene >> CDH5
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000341529 |
| Start |
66389454:66389454(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.713A>G |
| AA Mutation |
p.Asp238Gly(p.D238G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000341529 |
| Start |
66387087:66387087(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs370305306
|
| CDS Mutation |
c.489G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |