Variant #0000016740 (NC_000002.11:g.136547317del, NM_002299.2:c.5387del (LCT))
| Chromosome |
2 |
| Allele |
Paternal (confirmed) |
| 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.136547317del |
| DNA change (hg38) |
g.135789747del |
| Published as |
c.5387delA (p.D1796fs) |
| ISCN |
- |
| DB-ID |
LCT_000011 |
| Variant remarks |
1 Japanese family (com-het) with probable lactase deficiency, congenital |
| Reference |
PubMed: Uchida et al. 2012 |
| 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 |
2012-12-10 17:13:21 +01:00 (CET) |
| Date last edited |
2020-06-09 13:16:31 +02:00 (CEST) |

Variant on transcripts
|