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
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