Variant #0000809655 (NC_000022.10:g.41914532C>T, NM_001098.2:c.988C>T (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.41914532C>T
DNA change (hg38) -
Published as ACO2(NM_001098.2):c.988C>T (p.P330S), ACO2(NM_001098.3):c.988C>T (p.(Pro330Ser))
ISCN -
DB-ID ACO2_000011 See all 3 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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACO2 NM_001098.2 ?/. - c.988C>T r.(?) p.(Pro330Ser)
POLR3H NM_138338.3 ?/. - c.*10755G>A r.(=) p.(=)


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