Variant #0000677195 (NC_000004.11:g.128861068G>A, NM_152778.2:c.638C>T (MFSD8))

Chromosome 4
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.128861068G>A
DNA change (hg38) -
Published as MFSD8(NM_152778.4):c.638C>T (p.P213L)
ISCN -
DB-ID C4orf29_000014
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 2020-08-06 14:59:34 +02:00 (CEST)
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.-25711G>A r.(?) p.(=)
MFSD8 NM_152778.2 ?/. - c.638C>T r.(?) p.(Pro213Leu)


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