Variant #0000329058 (NC_000022.10:g.41926774T>C, NM_001098.2:c.*2157T>C (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.41926774T>C
DNA change (hg38) g.41530770T>C
Published as POLR3H(NM_001018050.2):c.478A>G (p.(Thr160Ala))
ISCN -
DB-ID POLR3H_000001
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-22 19:20:35 +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 ?/. 18_ c.*2157T>C r.(=) p.(=)
POLR3H NM_138338.3 ?/. - c.478A>G r.(?) p.(Thr160Ala)


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