Variant #0000018003 (NC_000017.10:g.8701172_8701174del, NM_152599.3:c.1266_1268del (MFSD6L))

Chromosome 17
Allele Parent #2
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.8701172_8701174del
DNA change (hg38) g.8797854_8797856del
Published as -
ISCN -
DB-ID MFSD6L_000001
Variant remarks variant marked as interesting (probably affects the function of the gene with phenotypic consequences) from an exome analysis. Please contact me.
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP 1
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2013-05-08 23:53:32 +02:00 (CEST)
Date last edited 2020-07-13 08:35:24 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MFSD6L NM_152599.3 ?/? ? c.1266_1268del r.(?) p.(Thr423del)



Screenings

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