Variant #0000874871 (NC_000001.10:g.183543638G>A, NM_000433.3:c.485C>T (NCF2))
Chromosome |
1 |
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.183543638G>A |
DNA change (hg38) |
g.183574503G>A |
Published as |
- |
ISCN |
- |
DB-ID |
NCF2_000057 |
Variant remarks |
- |
Reference |
PubMed: Roos 2021, Journal: Roos 2021 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2022-08-13 09:36:42 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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