Variant #0000969767 (NC_000019.9:g.41306666C>G, NM_053046.3:c.189C>G (EGLN2))

Chromosome 19
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.41306666C>G
DNA change (hg38) -
Published as EGLN2(NM_080732.4):c.189C>G (p.T63=)
ISCN -
DB-ID EGLN2_000004
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) 0.00013 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MIA NM_001202553.1 -?/. - c.*23341C>G r.(=) p.(=)
RAB4B NM_016154.4 -?/. - c.*4207C>G r.(=) p.(=)
EGLN2 NM_053046.3 -?/. - c.189C>G r.(?) p.(=)
RAB4B-EGLN2 NR_037791.1 -?/. - n.1237C>G r.(?) -


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