Gene >> FGB
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000302068 |
| Start |
154569288:154569288(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.939G>T |
| AA Mutation |
p.Lys313Asn(p.K313N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000302068 |
| Start |
154569620:154569620(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1065C>A |
| AA Mutation |
p.His355Gln(p.H355Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |