Variant #0001045056 (NC_000018.9:g.55222097G>A, NM_000140.3:c.892C>T (FECH))

Chromosome 18
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.55222097G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID FECH_000035
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2050848238
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-05-26 11:20:02 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FECH NM_000140.3 +/. - c.892C>T r.(?) p.(Arg298Ter)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.