Gene >> CADM2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000407528 |
| Start |
86065710:86065710(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1169G>A |
| AA Mutation |
p.Arg390Gln(p.R390Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000407528 |
| Start |
85912513:85912513(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.643C>G |
| AA Mutation |
p.Gln215Glu(p.Q215E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |