Variant #0000016228 (NC_000002.11:g.219525876C>T, NM_004328.4:c.166C>T (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.219525876C>T |
| DNA change (hg38) |
g.218661153C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
BCS1L_000002 |
| Variant remarks |
1 British patient (com-het) with GRACILE syndrome |
| Reference |
PubMed: Visapää et al. 2002 |
| ClinVar ID |
- |
| dbSNP ID |
rs121908576 |
| Origin |
SUMMARY record |
| Segregation |
? |
| Frequency |
0/140 CON |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00017 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 18:33:04 +02:00 (CEST) |

Variant on transcripts
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