Variant #0000036066 (NC_000012.11:g.64173879del, NM_014254.1:c.139del (TMEM5))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Effect unknown
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.64173879del
DNA change (hg38) g.63780099del
Published as -
ISCN -
DB-ID TMEM5_000007 See all 4 reported entries
Variant remarks expression cloning neither restored alpha-DG glycosylation nor enhanced susceptibility to infection with rVSV-GP-LASV
Reference PubMed: Jae 2013, OMIM:var0007
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
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 2014-03-22 17:06:02 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM5 NM_014254.1 +/? 1 c.139del r.(?) p.Ala47Argfs*42


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