Variant #0000521800 (NC_000004.11:g.151765894T>C, LRBA(NM_001199282.2):c.4377A>G)

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.151765894T>C
DNA change (hg38) g.150844742T>C
Published as LRBA(NM_001199282.2):c.4377A>G (p.Q1459=)
ISCN -
DB-ID LRBA_000082
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) 9.0E-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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRBA NM_001199282.2 -?/. - c.4377A>G r.(?) p.(Gln1459=)
MAB21L2 NM_006439.4 -?/. - c.*260633T>C r.(=) p.(=)