Variant #0000370061 (NC_000006.11:g.129687396G>A, NM_000426.3:c.4750G>A (LAMA2))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Classification method ACMG
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.129687396G>A
DNA change (hg38) g.129366251G>A
Published as -
ISCN -
DB-ID LAMA2_000123 See all 18 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) 0.01953 View details
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 09:12:31 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LAMA2 NM_000426.3 -?/-? 33 c.4750G>A r.(?) p.(Gly1584Ser)


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