Variant #0000282068 (NC_000001.10:g.209811896C>T, LAMB3(NM_000228.2):c.281G>A)

Chromosome 1
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.209811896C>T
DNA change (hg38) g.209638551C>T
Published as LAMB3(NM_001017402.2):c.281G>A (p.W94*)
ISCN -
DB-ID LAMB3_000017
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LAMB3 NM_000228.2 +/. - c.281G>A r.(?) p.(Trp94Ter)