Variant #0001031408 (NC_000001.10:g.161133956A>G, NM_000309.3:c.-2454A>G (PPOX))

Chromosome 1
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.161133956A>G
DNA change (hg38) -
Published as USP21(NM_001014443.3):c.1221A>G (p.(Lys407=))
ISCN -
DB-ID B4GALT3_000012
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) 0.00021 View details
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPOX NM_000309.3 ?/. - c.-2454A>G r.(?) p.(=)
USP21 NM_001014443.2 ?/. - c.1221A>G r.(?) p.(=)
B4GALT3 NM_003779.3 ?/. - c.*7650T>C r.(=) p.(=)


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