Variant #0001043902 (NC_000022.10:g.41940441_41940442insCGCGCACCGC, NM_001098.2:c.*15824_*15825insCGCGCACCGC (ACO2))

Chromosome 22
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.41940441_41940442insCGCGCACCGC
DNA change (hg38) -
Published as POLR3H(NM_001282885.2):c.-23_-22insCGGTGCGCGG
ISCN -
DB-ID ACO2_000179
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACO2 NM_001098.2 ?/. - c.*15824_*15825insCGCGCACCGC r.(=) p.(=)
POLR3H NM_138338.3 ?/. - c.-30_-29insCGGTGCGCGG r.(?) p.(=)


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