Variant #0000291088 (NC_000004.11:g.151821326C>T, NM_001199282.2:c.1799G>A (LRBA))

Chromosome 4
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.151821326C>T
DNA change (hg38) g.150900174C>T
Published as LRBA(NM_001199282.2):c.1799G>A (p.G600D)
ISCN -
DB-ID LRBA_000034
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 2018-01-15 20:58:59 +01:00 (CET)
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.1799G>A r.(?) p.(Gly600Asp)
LRBA NM_001364905.1 ?/. - c.1799G>A r.(?) p.(Gly600Asp)
MAB21L2 NM_006439.4 ?/. - c.*316065C>T r.(=) p.(=)


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