Variant #0001046466 (NC_000014.8:g.20920511A>G, NM_017807.3:c.212T>C (OSGEP))

Chromosome 14
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.20920511A>G
DNA change (hg38) -
Published as OSGEP(NM_017807.4):c.212T>C (p.I71T)
ISCN -
DB-ID APEX1_000003
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) 0.0001 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-07-08 13:22:38 +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     
APEX1 NM_001641.3 ?/. - c.-3111A>G r.(?) p.(=)
OSGEP NM_017807.3 ?/. - c.212T>C r.(?) p.(Ile71Thr)


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