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 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-08-13 09:36:42 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NCF2 NM_000433.3 -/. - c.485C>T r.(?) p.(Ala162Val)


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