Variant #0000677928 (NC_000007.13:g.107577680_107577681dup, NM_002291.2:c.3803_3804dup (LAMB1))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.107577680_107577681dup
DNA change (hg38) -
Published as LAMB1(NM_002291.3):c.3803_3804dupAA (p.V1269Kfs*2)
ISCN -
DB-ID LAMB1_000059
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-08-06 14:59:34 +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     
LAMB1 NM_002291.2 +?/. - c.3803_3804dup r.(?) p.(Val1269LysfsTer2)


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