Variant #0000881504 (NC_000006.11:g.132196989A>G, NM_006208.2:c.1709A>G (ENPP1))

Chromosome 6
Allele Parent #1
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.132196989A>G
DNA change (hg38) g.131875849A>G
Published as -
ISCN -
DB-ID ENPP1_000018 See all 6 reported entries
Variant remarks -
Reference PubMed: Mercurio 2022, Journal: Mercurio 2022
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-10-23 14:20:36 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ENPP1 NM_006208.2 +?/. 17 c.1709A>G r.(?) p.Tyr570Cys


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.