Variant #0000521665 (NC_000004.11:g.128859942T>C, NM_152778.2:c.750A>G (MFSD8))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.128859942T>C
DNA change (hg38) g.127938787T>C
Published as MFSD8(NM_152778.2):c.750A>G (p.E250=)
ISCN -
DB-ID C4orf29_000008 See all 5 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) 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-16 14:50:55 +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.-26837T>C r.(?) p.(=)
MFSD8 NM_152778.2 -?/. - c.750A>G r.(?) p.(Glu250=)


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