Variant #0000848582 (NC_000001.10:g.231471908A>G, NM_022051.2:c.*30249T>C (EGLN1))

Chromosome 1
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.231471908A>G
DNA change (hg38) -
Published as EXOC8(NM_175876.5):c.1584T>C (p.H528=)
ISCN -
DB-ID EGLN1_000030
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) 0.0018 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 2022-05-09 15:40:45 +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     
EGLN1 NM_022051.2 -?/. - c.*30249T>C r.(=) p.(=)
SPRTN NM_032018.5 -?/. - c.-2222A>G r.(?) p.(=)
EXOC8 NM_175876.3 -?/. - c.1584T>C r.(?) p.(His528=)


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