Variant #0000286040 (NC_000004.11:g.151837665T>C, NM_001199282.2:c.782A>G (LRBA))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.151837665T>C
DNA change (hg38) g.150916513T>C
Published as LRBA(NM_001199282.2):c.782A>G (p.K261R), LRBA(NM_001364905.1):c.782A>G (p.(Lys261Arg))
ISCN -
DB-ID LRBA_000040 See all 2 reported entries
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) 4.0E-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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRBA NM_001199282.2 -?/. - c.782A>G r.(?) p.(Lys261Arg)
LRBA NM_001364905.1 -?/. - c.782A>G r.(?) p.(Lys261Arg)
MAB21L2 NM_006439.4 -?/. - c.*332404T>C r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.