Variant #0000719757 (NC_000004.11:g.128851987dup, NC_000004.11(NM_152778.2):c.864-6dup (MFSD8))

Chromosome 4
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.128851987dup
DNA change (hg38) -
Published as MFSD8(NM_152778.4):c.864-6dupT
ISCN -
DB-ID C4orf29_000021 See all 2 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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.-34792dup r.(?) p.(=)
MFSD8 NM_152778.2 -/. - c.864-6dup r.(=) p.(=)


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