Variant #0001057193 (NC_000022.10:g.41863531del, NM_001098.2:c.-1620del (ACO2))

Chromosome 22
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.41863531del
DNA change (hg38) -
Published as PHF5A(NM_032758.4):c.164del (p.(Gln55Argfs*5))
ISCN -
DB-ID ACO2_000180
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     
ACO2 NM_001098.2 +?/. - c.-1620del r.(?) p.(=)
PHF5A NM_032758.3 +?/. - c.164del r.(?) p.(Gln55Argfs*5)
POLR3H NM_138338.3 +?/. - c.*61756del r.(?) p.(=)


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