Variant #0000016227 (NC_000002.11:g.219525123T>A, NC_000002.11(NM_004328.4):c.-50+155T>A (BCS1L))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.219525123T>A |
| DNA change (hg38) |
g.218660400T>A |
| Published as |
intron 1, -588T>A |
| ISCN |
- |
| DB-ID |
BCS1L_000001 |
| Variant remarks |
1 British patient (com-het) with GRACILE syndrome; pathogenicity not confirmed |
| Reference |
PubMed: Visapää et al. 2002 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
? |
| Frequency |
0/140 CON |
| 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 |
2012-11-13 12:27:28 +01:00 (CET) |
| Date last edited |
2020-06-11 15:28:23 +02:00 (CEST) |

Variant on transcripts
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