Variant #0000527158 (NC_000006.11:g.129722453C>A, NM_000426.3:c.5530C>A (LAMA2))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.129722453C>A
DNA change (hg38) g.129401308C>A
Published as LAMA2(NM_000426.3):c.5530C>A (p.(Arg1844Ser), p.R1844S), LAMA2(NM_000426.4):c.5530C>A (p.R1844S)
ISCN -
DB-ID LAMA2_000092 See all 14 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.01041 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +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 -?/. - c.5530C>A r.(?) p.(Arg1844Ser)


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