Variant #0000881551 (NC_000006.11:g.132129152G>C, NM_006208.2:c.-24G>C (ENPP1))

Chromosome 6
Allele Parent #1
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.132129152G>C
DNA change (hg38) g.131808012G>C
Published as -
ISCN -
DB-ID ENPP1_000091 See all 2 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) 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 2022-10-23 14:20:36 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ENPP1 NM_006208.2 ?/. 1 c.-24G>C r.(?) p.?


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