Variant #0000286574 (NC_000004.11:g.128878744T>A, NM_152778.2:c.66A>T (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.128878744T>A
DNA change (hg38) g.127957589T>A
Published as MFSD8(NM_152778.2):c.66A>T (p.E22D), MFSD8(NM_152778.3):c.66A>T (p.E22D), MFSD8(NM_152778.4):c.66A>T (p.E22D)
ISCN -
DB-ID MFSD8_000038 See all 3 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) 0.00223 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-11-27 17:27:23 +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.-8035T>A r.(?) p.(=)
MFSD8 NM_152778.2 -?/. - c.66A>T r.(?) p.(Glu22Asp)


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