Variant #0000003015 (NC_000007.14:g.8306_8307delGT, NM_000265.7:c.75_76delGT (NCF1))

Individual ID 00000753
Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.8306_8307delGT
Published as -
Reference Harvindar Kaur Gill et al.(2012)
DB-ID NCF1_000001
dbSNP ID -
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nur Aisyah Athirah
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nur Aisyah Athirah
Date created 2021-07-04 15:43:52 +08:00 (CST)
Date last edited 2021-08-01 13:20:02 +08:00 (CST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

Clinical classification     
NCF1 NM_000265.7 +/. 2 c.75_76delGT - r.(?) p.(Tyr26Hisfs*26) -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000847 DNA PCR;RT-PCR;SEQ NCF1 1 Nur Aisyah Athirah