Variant #0000655097 (NC_000004.11:g.128842888C>A, NM_152778.2:c.1141G>T (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.128842888C>A
DNA change (hg38) g.127921733C>A
Published as MFSD8(NM_152778.2):c.1141G>T (p.E381*)
ISCN -
DB-ID MFSD8_000012 See all 7 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-06-16 14:49:52 +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.-43891C>A r.(?) p.(=)
MFSD8 NM_152778.2 +/. - c.1141G>T r.(?) p.(Glu381Ter)


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