Gene >> CELF2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000416382 |
| Start |
11270694:11270694(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.626T>C |
| AA Mutation |
p.Phe209Ser(p.F209S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000416382 |
| Start |
11321267:11321267(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1136C>T |
| AA Mutation |
p.Thr379Ile(p.T379I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |