Gene >> CDH5
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000341529 |
| Start |
66400884:66400884(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1705A>G |
| AA Mutation |
p.Ser569Gly(p.S569G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000341529 |
| Start |
66398072:66398072(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1451A>T |
| AA Mutation |
p.Gln484Leu(p.Q484L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |