Gene >> SMARCA2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000349721 |
| Start |
2058298:2058298(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1355T>C |
| AA Mutation |
p.Leu452Pro(p.L452P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant;splice_region_variant |
| Transcription ID |
ENST00000349721 |
| Start |
2161902:2161902(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4198A>G |
| AA Mutation |
p.Arg1400Gly(p.R1400G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |