Gene >> FSCN1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000382361 |
| Start |
5593072:5593072(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.136T>C |
| AA Mutation |
p.Trp46Arg(p.W46R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000382361 |
| Start |
5605458:5605458(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1466C>T |
| AA Mutation |
p.Ser489Leu(p.S489L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |