Variant #0000521664 (NC_000004.11:g.128854139C>T, NC_000004.11(NM_152778.2):c.863+1G>A (MFSD8))

Chromosome 4
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.128854139C>T
DNA change (hg38) g.127932984C>T
Published as MFSD8(NM_152778.2):c.863+1G>A (p.?)
ISCN -
DB-ID MFSD8_000056 See all 4 reported entries
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) 0 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-16 14:50:40 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C4orf29 NM_001039717.1 +/. - c.-32640C>T r.(?) p.(=)
MFSD8 NM_152778.2 +/. - c.863+1G>A r.spl? p.?


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