Variant #0000881552 (NC_000006.11:g.(132173376_132176065)_(132176164_132179807)del, NC_000006.11(NM_006208.2):c.(617+1_618-1)_(715+1_716-1)del (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.(132173376_132176065)_(132176164_132179807)del
DNA change (hg38) g.(131852236_131854925)_(131855024_131858667)del
Published as del ex6
ISCN -
DB-ID LAMA2_000000 See all 127 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 2022-10-23 15:03:49 +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 +/. 5i_6i c.(617+1_618-1)_(715+1_716-1)del r.? p.?


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