Variant #0000859257 (NC_000004.11:g.151817586dup, NM_001199282.2:c.2028dup (LRBA))

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.151817586dup
DNA change (hg38) -
Published as LRBA(NM_006726.4):c.2028dupA (p.L677Ifs*6)
ISCN -
DB-ID LRBA_000156
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRBA NM_001199282.2 +/. - c.2028dup r.(?) p.(Leu677Ilefs*6)
LRBA NM_001364905.1 +/. - c.2028dup r.(?) p.(Leu677Ilefs*6)
MAB21L2 NM_006439.4 +/. - c.*312325dup r.(?) p.(=)


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