Variant #0000003199 (NC_000007.14:g.74191610C>A, NC_000007.14(NM_000265.7):c.73-3C>A (NCF1))

Individual ID 00000832
Chromosome 7
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.74191610C>A
Published as NCF1
Reference Intan Juliana Abd Hamid et al. (2020)
DB-ID NCF1_000002
dbSNP ID rs377305075
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) 0.00029 View details
Owner Noorzalifah Binti Mazuki
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Noorzalifah Binti Mazuki
Date created 2021-08-10 12:52:54 +08:00 (CST)
Date last edited 2022-01-25 09:34:50 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

Clinical classification     
NCF1 NM_000265.7 ?/. - c.73-3C>A NCF1 r.spl? p.? ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000948 DNA ? NCF1 1 Noorzalifah Binti Mazuki