Variant #0000294269 (NC_000001.10:g.161137920G>A, NC_000001.10(NM_000309.3):c.471+3G>A (PPOX))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.161137920G>A
DNA change (hg38) g.161168130G>A
Published as PPOX(NM_001122764.3):c.471+3G>A
ISCN -
DB-ID PPOX_000005
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) 0.00022 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 2020-06-05 14:17:22 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPOX NM_000309.3 -?/. - c.471+3G>A r.spl? p.?
USP21 NM_001014443.2 -?/. - c.*2683G>A r.(=) p.(=)
B4GALT3 NM_003779.3 -?/. - c.*3686C>T r.(=) p.(=)


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