Variant #0000876130 (NC_000022.10:g.37270502A>G, NC_000022.10(NM_000631.4):c.628-1193A>G (NCF4))

Chromosome 22
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.37270502A>G
DNA change (hg38) g.36874460A>G
Published as -
ISCN -
DB-ID NCF4_000048
Variant remarks -
Reference PubMed: Roos 2010, Journal: Roos 2010
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-08-14 12:01:16 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NCF4 NM_000631.4 -/. - c.628-1193A>G r.(?) p.(=)


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