Variant #0000874619 (NC_000001.10:g.231557513T>C, NM_022051.2:c.122A>G (EGLN1))

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.231557513T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID EGLN1_000031
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1365297757
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-08-10 12:12:01 +02:00 (CEST)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EGLN1 NM_022051.2 ?/. - c.122A>G r.(?) p.(Tyr41Cys)


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