Variant #0000331799 (NC_000007.13:g.107564435_107564436dup, NM_002291.2:c.5324_5325dup (LAMB1))

Chromosome 7
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.107564435_107564436dup
DNA change (hg38) g.107923990_107923991dup
Published as LAMB1(NM_002291.2):c.5325_5326insTA (p.(Ser1776Ter))
ISCN -
DB-ID LAMB1_000003
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-23 13:27:50 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DLD NM_000108.3 ?/. - c.*4731_*4732dup r.(=) p.(=)
LAMB1 NM_002291.2 ?/. - c.5324_5325dup r.(?) p.(Ser1776Ter)


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