Gene >> CTNNAL1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000325551 |
| Start |
108943019:108943019(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2081G>C |
| AA Mutation |
p.Arg694Thr(p.R694T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000325551 |
| Start |
108979458:108979458(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.924G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |