Variant #0000016738 (NC_000002.11:g.136558209C>A, NM_002299.2:c.4834G>T (LCT))
Chromosome |
2 |
Allele |
Paternal (confirmed) |
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.136558209C>A |
DNA change (hg38) |
g.135800639C>A |
Published as |
c.4834G>T (E1612X) |
ISCN |
- |
DB-ID |
LCT_000009 |
Variant remarks |
1 Italian family (com-het) with lactase deficiency, congenital |
Reference |
PubMed: Torniainen et al. 2009 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
yes |
Frequency |
0/101 ITA 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 |
2012-12-10 17:13:21 +01:00 (CET) |
Date last edited |
2019-07-02 08:01:36 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|