Variant #0000677210 (NC_000004.11:g.151829906T>C, NM_001199282.2:c.1265A>G (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.151829906T>C
DNA change (hg38) -
Published as LRBA(NM_001199282.2):c.1265A>G (p.N422S)
ISCN -
DB-ID LRBA_000119
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-08-06 14:59:34 +02:00 (CEST)
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.1265A>G r.(?) p.(Asn422Ser)
LRBA NM_001364905.1 ?/. - c.1265A>G r.(?) p.(Asn422Ser)
MAB21L2 NM_006439.4 ?/. - c.*324645T>C r.(=) p.(=)


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