Variant #0000521666 (NC_000004.11:g.128865037T>A, NM_152778.2:c.309A>T (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.128865037T>A
DNA change (hg38) g.127943882T>A
Published as MFSD8(NM_152778.2):c.309A>T (p.(Arg103Ser))
ISCN -
DB-ID C4orf29_000009
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) 7.0E-5 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C4orf29 NM_001039717.1 +?/. - c.-21742T>A r.(?) p.(=)
MFSD8 NM_152778.2 +?/. - c.309A>T r.(?) p.(Arg103Ser)


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