Variant #0000021430 (NC_000019.9:g.10426672T>A, NM_001031734.2:c.1A>T (FDX1L))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Effect unknown
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.10426672T>A
DNA change (hg38) g.10315996T>A
Published as -
ISCN -
DB-ID FDX1L_000001 See all 2 reported entries
Variant remarks 1/288 control chromosomes (ethnic match)
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Ronen Spiegel
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2013-10-12 23:09:10 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FDX1L NM_001031734.2 +/? 1 c.1A>T r.(?) p.0?


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