Variant #0000367751 (NC_000013.10:g.101736075A>G, NM_052867.2:c.3570T>C (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.101736075A>G |
DNA change (hg38) |
g.101083724A>G |
Published as |
- |
ISCN |
- |
DB-ID |
NALCN_000023 See all 2 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs686141 |
Origin |
Unknown |
Segregation |
? |
Frequency |
0.73 controls |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.68703 View details |
Owner |
Florian Erger |
Database submission license |
No license selected |
Created by |
Florian Erger |
Date created |
2018-04-03 17:40:36 +02:00 (CEST) |
Date last edited |
2018-04-06 09:43:15 +02:00 (CEST) |

Variant on transcripts
Screenings
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