Variant #0000578982 (NC_000006.11:g.132206079C>T, NM_006208.2:c.2320C>T (ENPP1))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.132206079C>T
DNA change (hg38) g.131884939C>T
Published as -
ISCN -
DB-ID ENPP1_000003 See all 17 reported entries
Variant remarks cDNA expression cloning HEK293/COS7 cells, 0.57 NPP enzyme activity/0.75 PPi generation, 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) 0.03358 View details
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 10:24:13 +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.2320C>T r.(?) p.Arg774Cys


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