Variant #0000370091 (NC_000006.11:g.129371106C>T, NM_000426.3:c.156C>T (LAMA2))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method ACMG
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.129371106C>T
DNA change (hg38) g.129049961C>T
Published as -
ISCN -
DB-ID LAMA2_000153 See all 6 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) 0.09868 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 09:11:11 +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 -/- 2 c.156C>T r.(?) p.(=)


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