Variant #0001078411 (NC_000009.11:g.133779564G>A, NM_032843.4:c.1273C>T (FIBCD1))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.133779564G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID FIBCD1_000004
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs533919875
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-06-05 10:22:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FIBCD1 NM_032843.4 ?/. - c.1273C>T r.(?) p.(Arg425Cys)


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