Variant #0000370247 (NC_000006.11:g.129799959G>A, NC_000006.11(NM_000426.3):c.7572+1G>A (LAMA2))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method ACMG
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.129799959G>A
DNA change (hg38) g.129478814G>A
Published as -
ISCN -
DB-ID LAMA2_000312 See all 4 reported entries
Variant remarks -
Reference PubMed: Oliveira 2018, Journal: Oliveira 2018
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Jorge Oliveira
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2018-06-29 15:10:22 +02:00 (CEST)
Date last edited 2020-06-22 08:55:48 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LAMA2 NM_000426.3 +/+ 54i c.7572+1G>A r.spl p.?


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