Variant #0001022246 (NC_000004.11:g.128859942T>C, NM_152778.2:c.750A>G (MFSD8))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.128859942T>C
DNA change (hg38) g.127938787T>C
Published as -
ISCN -
DB-ID C4orf29_000008 See all 5 reported entries
Variant remarks in vitro analysis 293T cells mini-gene exon trapping assay: effect on RNA exon skipping
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Tjakko van Ham
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2024-11-05 16:15:00 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MFSD8 NM_152778.2 +?/. 7 c.750A>G r.699_754del p.Arg233SerfsTer5


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