Variant #0000609089 (NC_000004.11:g.151829580T>C, NM_001199282.2:c.1399A>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.151829580T>C
DNA change (hg38) g.150908428T>C
Published as LRBA(NM_001199282.2):c.1399A>G (p.(Met467Val), p.M467V), LRBA(NM_001367550.1):c.1399A>G (p.M467V)
ISCN -
DB-ID LRBA_000096 See all 4 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) 0.00211 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 14:54:23 +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.1399A>G r.(?) p.(Met467Val)
LRBA NM_001364905.1 -?/. - c.1399A>G r.(?) p.(Met467Val)
MAB21L2 NM_006439.4 -?/. - c.*324319T>C r.(=) p.(=)


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