Variant #0000885899 (NC_000003.11:g.49160671T>C, NM_002292.3:c.4118A>G (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.49160671T>C
DNA change (hg38) -
Published as LAMB2(NM_002292.3):c.4118A>G (p.D1373G), LAMB2(NM_002292.4):c.4118A>G (p.(Asp1373Gly), p.D1373G)
ISCN -
DB-ID LAMB2_000066 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) 0.00093 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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
LAMB2 NM_002292.3 -?/. - c.4118A>G r.(?) p.(Asp1373Gly) -
USP19 NM_006677.2 -?/. - c.-2619A>G r.(?) p.(=) -


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