Variant #0000520186 (NC_000003.11:g.49162733G>A, NM_002292.3:c.2673C>T (LAMB2))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.49162733G>A
DNA change (hg38) g.49125300G>A
Published as LAMB2(NM_002292.4):c.2673C>T (p.G891=)
ISCN -
DB-ID LAMB2_000044 See all 2 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) 0.00857 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +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.2673C>T r.(?) p.(Gly891=) -
USP19 NM_006677.2 -/. - c.-4681C>T r.(?) p.(=) -


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