Variant #0000975898 (NC_000003.11:g.49169782G>A, NM_002292.3:c.306C>T (LAMB2))

Chromosome 3
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.49169782G>A
DNA change (hg38) -
Published as LAMB2(NM_002292.3):c.306C>T, LAMB2(NM_002292.4):c.306C>T (p.(Asn102=), p.N102=)
ISCN -
DB-ID LAMB2_000008 See all 4 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) 0.02222 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
LAMB2 NM_002292.3 -?/. - c.306C>T r.(?) p.(Asn102=) -


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