Variant #0001068946 (NC_000018.9:g.55233696T>C, NM_000140.3:c.581A>G (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.55233696T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID FECH_000037
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2511532623
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 2026-03-04 16:29:02 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FECH NM_000140.3 +/. - c.581A>G r.(?) p.(Tyr194Cys)


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