Variant #0000520178 (NC_000003.11:g.49160137G>A, NM_002292.3:c.4573C>T (LAMB2))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.49160137G>A
DNA change (hg38) g.49122704G>A
Published as LAMB2(NM_002292.3):c.4573C>T (p.Q1525*)
ISCN -
DB-ID LAMB2_000111
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-15 09:54:23 +02:00 (CEST)
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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.4573C>T r.(?) p.(Gln1525Ter) -
USP19 NM_006677.2 ?/. - c.-2085C>T r.(?) p.(=) -


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