Variant #0000791889 (NC_000006.11:g.129807757C>T, NM_000426.3:c.7888C>T (LAMA2))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.129807757C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID LAMA2_000359 See all 6 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs727502851
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-08-02 16:06:01 +02:00 (CEST)
Date last edited 2022-09-26 12:22:42 +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 +/. - c.7888C>T r.(?) p.(Arg2630Ter)


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