Variant #0000881541 (NC_000006.11:g.132129201dup, NM_006208.2:c.26dup (ENPP1))
Chromosome |
6 |
Allele |
Parent #1 |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
ACMG |
Clinical classification |
pathogenic (recessive) |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.132129201dup |
DNA change (hg38) |
g.131808061dup |
Published as |
- |
ISCN |
- |
DB-ID |
ENPP1_000087 See all 4 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 International |
Created by |
Johan den Dunnen |
Date created |
2022-10-23 14:20:36 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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