Variant #0001034370 (NC_000004.11:g.151504620G>T, NC_000004.11(NM_001199282.2):c.6330+4580C>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.151504620G>T
DNA change (hg38) -
Published as LRBA(NM_006726.4):c.6363+4580C>A, MAB21L2(NM_006439.5):c.439G>T (p.(Asp147Tyr), p.D147Y)
ISCN -
DB-ID LRBA_000121 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRBA NM_001199282.2 ?/. - c.6330+4580C>A r.(=) p.(=)
LRBA NM_001364905.1 ?/. - c.6330+4580C>A r.(=) p.(=)
MAB21L2 NM_006439.4 ?/. - c.439G>T r.(?) p.(Asp147Tyr)


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