Variant #0000689234 (NC_000004.11:g.128842710del, NM_152778.2:c.1319del (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.128842710del
DNA change (hg38) -
Published as MFSD8(NM_152778.2):c.1319delT (p.L440Hfs*6)
ISCN -
DB-ID C4orf29_000017
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C4orf29 NM_001039717.1 +?/. - c.-44069del r.(?) p.(=)
MFSD8 NM_152778.2 +?/. - c.1319del r.(?) p.(Leu440HisfsTer6)


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