Variant #0000036141 (NC_000002.11:g.219526006C>T, NM_004328.4:c.296C>T (BCS1L))
| Chromosome |
2 |
| Allele |
Both (homozygous) |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.219526006C>T |
| DNA change (hg38) |
g.218661283C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
BCS1L_000007 |
| Variant remarks |
1 patient (hom) with GRACILE syndrome |
| Reference |
PubMed: Kasapkara et al. 2014 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Anne Polvi |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Anne Polvi |
| Date created |
2014-04-03 16:29:23 +02:00 (CEST) |
| Date last edited |
2017-05-05 19:04:32 +02:00 (CEST) |

Variant on transcripts
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