Variant #0000677209 (NC_000004.11:g.151789460G>T, NC_000004.11(NM_001199282.2):c.2450-3C>A (LRBA))

Chromosome 4
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.151789460G>T
DNA change (hg38) -
Published as LRBA(NM_001199282.2):c.2450-3C>A
ISCN -
DB-ID LRBA_000118
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) 1.0E-5 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 2020-08-06 14:59:34 +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.2450-3C>A r.spl? p.?
LRBA NM_001364905.1 +?/. - c.2450-3C>A r.spl? p.?
MAB21L2 NM_006439.4 +?/. - c.*284199G>T r.(=) p.(=)


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