Variant #0000874847 (NC_000022.10:g.?, NM_000631.4:c.? (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.?
DNA change (hg38) -
Published as 815C>T (P272L), 815G>A (P272L)
ISCN -
DB-ID NCF4_000000
Variant remarks -
Reference PubMed: Roos 2021, Journal: Roos 2021, PubMed: Lee 2006, Journal: Lee 2006
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
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 08:55:00 +02:00 (CEST)
Date last edited 2022-08-13 08:55:49 +02:00 (CEST)




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NCF4 NM_000631.4 -/. - c.? r.(?) p.(?)


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