Gene >> GSK3B
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264235 |
| Start |
119863592:119863592(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs775606264
|
| CDS Mutation |
c.923G>A |
| AA Mutation |
p.Arg308Gln(p.R308Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264235 |
| Start |
120093379:120093379(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.56A>G |
| AA Mutation |
p.Gln19Arg(p.Q19R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |