Variant #0000285863 (NC_000018.9:g.7046293C>T, NM_005559.3:c.842G>A (LAMA1))

Chromosome 18
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.7046293C>T
DNA change (hg38) g.7046294C>T
Published as LAMA1(NM_005559.3):c.842G>A (p.W281*), LAMA1(NM_005559.4):c.842G>A (p.W281*)
ISCN -
DB-ID LAMA1_000095 See all 2 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LAMA1 NM_005559.3 +/. - c.842G>A r.(?) p.(Trp281Ter)


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