Variant #0000578989 (NC_000006.11:g.132181633A>G, NM_006208.2:c.902A>G (ENPP1))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.132181633A>G
DNA change (hg38) g.131860493A>G
Published as -
ISCN -
DB-ID ENPP1_000008 See all 3 reported entries
Variant remarks cDNA expression cloning HEK293/COS7 cells, no NPP enzyme activity/PPi generation, no localisation plasma membrane
Reference PubMed: Stella 2016
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Yvonne Nitschke
Database submission license No license selected
Created by Yvonne Nitschke
Date created 2016-07-15 10:44:28 +02:00 (CEST)
Date last edited 2020-06-22 10:24:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ENPP1 NM_006208.2 +/. - c.902A>G r.(?) p.Tyr301Cys


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