Variant #0000859075 (NC_000003.11:g.49159190C>A, NM_002292.3:c.5027G>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.49159190C>A
DNA change (hg38) -
Published as LAMB2(NM_002292.4):c.5027G>T (p.G1676V)
ISCN -
DB-ID LAMB2_000146
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) 0.00146 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 2022-05-09 15:51:19 +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.5027G>T r.(?) p.(Gly1676Val) -
USP19 NM_006677.2 -?/. - c.-1138G>T r.(?) p.(=) -


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