Variant #0000716943 (NC_000001.10:g.161138908G>C, NM_000309.3:c.742G>C (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.161138908G>C
DNA change (hg38) -
Published as PPOX(NM_001350130.1):c.256G>C (p.G86R), PPOX(NM_001350130.2):c.256G>C (p.G86R)
ISCN -
DB-ID B4GALT3_000005 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) 1.0E-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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.742G>C r.(?) p.(Gly248Arg)
USP21 NM_001014443.2 ?/. - c.*3671G>C r.(=) p.(=)
B4GALT3 NM_003779.3 ?/. - c.*2698C>G r.(=) p.(=)


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