Variant #0001034367 (NC_000004.11:g.151271250T>G, NM_001199282.2:c.7256A>C (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.151271250T>G
DNA change (hg38) -
Published as LRBA(NM_001364905.1):c.7256A>C (p.(Tyr2419Ser))
ISCN -
DB-ID LRBA_000188
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_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.7256A>C r.(?) p.(Tyr2419Ser)
LRBA NM_001364905.1 ?/. - c.7256A>C r.(?) p.(Tyr2419Ser)
MAB21L2 NM_006439.4 ?/. - c.-232932T>G r.(?) p.(=)


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