Variant #0000344239 (NC_000014.8:g.20920216A>G, NM_017807.3:c.328T>C (OSGEP))

Chromosome 14
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.20920216A>G
DNA change (hg38) g.20452057A>G
Published as OSGEP(NM_017807.4):c.328T>C (p.C110R)
ISCN -
DB-ID OSGEP_000002 See all 9 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) 0.00029 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APEX1 NM_001641.3 +/. - c.-3406A>G r.(?) p.(=)
OSGEP NM_017807.3 +/. - c.328T>C r.(?) p.(Cys110Arg)


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