Variant #0000689236 (NC_000004.11:g.128878732T>C, NM_152778.2:c.78A>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.128878732T>C
DNA change (hg38) -
Published as MFSD8(NM_152778.2):c.78A>G (p.L26=)
ISCN -
DB-ID C4orf29_000019
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) 2.0E-5 View details
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.-8047T>C r.(?) p.(=)
MFSD8 NM_152778.2 -?/. - c.78A>G r.(?) p.(Leu26=)


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