Variant #0000294270 (NC_000001.10:g.161139738G>A, NM_000309.3:c.911G>A (PPOX))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.161139738G>A
DNA change (hg38) g.161169948G>A
Published as PPOX(NM_000309.4):c.911G>A (p.R304H), PPOX(NM_001122764.3):c.911G>A (p.R304H)
ISCN -
DB-ID PPOX_000008 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) 0.0584 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 14:54:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPOX NM_000309.3 -/. - c.911G>A r.(?) p.(Arg304His)
USP21 NM_001014443.2 -/. - c.*4501G>A r.(=) p.(=)
B4GALT3 NM_003779.3 -/. - c.*1868C>T r.(=) p.(=)


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