Variant #0000369958 (NC_000006.11:g.129573237_129573241del, NM_000426.3:c.1893_1897del (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.129573237_129573241del
DNA change (hg38) g.129252092_129252096del
Published as -
ISCN -
DB-ID LAMA2_000017 See all 8 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 2019-02-28 09:09:39 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LAMA2 NM_000426.3 +/+ 14 c.1893_1897del r.(?) p.(Asp631Glufs*8)


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.