Variant #0001054005 (NC_000011.9:g.76376910_76376911dup, NC_000011.9(NM_005512.2):c.84+5_84+6dup (LRRC32))

Chromosome 11
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.76376910_76376911dup
DNA change (hg38) -
Published as LRRC32(NM_001370189.1):c.-1_1dup (p.(Met1?))
ISCN -
DB-ID LRRC32_000006
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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRRC32 NM_005512.2 ?/. - c.84+5_84+6dup r.spl? p.?


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