Variant #0000572165 (NC_000022.10:g.41864657T>A, NM_001098.2:c.-494T>A (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.41864657T>A
DNA change (hg38) g.41468653T>A
Published as -
ISCN -
DB-ID ACO2_000032 See all 2 reported entries
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-17 13:45:44 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACO2 NM_001098.2 ?/. _1 c.-494T>A r.(?) p.(=)
PHF5A NM_032758.3 ?/. - c.1A>T r.(?) p.(Met1?)
POLR3H NM_138338.3 ?/. - c.*60630A>T r.(=) p.(=)


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