Variant #0000367750 (NC_000013.10:g.101735211G>A, NM_052867.2:c.3714C>T (NALCN))
Individual ID |
00163650 |
Chromosome |
13 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.101735211G>A |
DNA change (hg38) |
g.101082860G>A |
Published as |
- |
ISCN |
- |
DB-ID |
NALCN_000022 See all 2 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs17677552 |
Origin |
Unknown |
Segregation |
? |
Frequency |
0.37 controls |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.35142 View details |
Owner |
Florian Erger |
Database submission license |
No license selected |
Created by |
Florian Erger |
Date created |
2018-04-03 17:38:28 +02:00 (CEST) |
Date last edited |
2018-04-06 09:40:51 +02:00 (CEST) |

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