Variant #0000016229 (NC_000002.11:g.219525942A>G, NM_004328.4:c.232A>G (BCS1L))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.219525942A>G |
| DNA change (hg38) |
g.218661219A>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
BCS1L_000003 See all 2 reported entries |
| Variant remarks |
functional studies, variant causes functional defect in BCS1L protein; Finnish Major GRACILE mutation: 11 Finnish GRACILE families (hom) and 3 Finnish GRACILE patients (hom), also 1 British GRACILE patient (com-het) |
| Reference |
PubMed: Visapää et al. 2002, PubMed: Fellman et al. 2008 |
| ClinVar ID |
- |
| dbSNP ID |
rs28937590 |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
1/494 FIN (het) |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.0005 View details |
| Owner |
Anne Polvi |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Anne Polvi |
| Date created |
2012-11-13 12:27:28 +01:00 (CET) |
| Date last edited |
2017-05-05 19:04:32 +02:00 (CEST) |

Variant on transcripts
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