Variant #0000975895 (NC_000003.11:g.49162583C>T, NM_002292.3:c.2740G>A (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.49162583C>T
DNA change (hg38) -
Published as LAMB2(NM_002292.4):c.2740G>A (p.(Gly914Arg), p.G914R)
ISCN -
DB-ID LAMB2_000045 See all 5 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) 0.03185 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.2740G>A r.(?) p.(Gly914Arg) -
USP19 NM_006677.2 -?/. - c.-4531G>A r.(?) p.(=) -


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