Variant #0000799163 (NC_000001.10:g.231473430C>A, NM_022051.2:c.*28727G>T (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.231473430C>A
DNA change (hg38) -
Published as EXOC8(NM_175876.4):c.62G>T (p.G21V)
ISCN -
DB-ID EGLN1_000028
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +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.*28727G>T r.(=) p.(=)
SPRTN NM_032018.5 ?/. - c.-700C>A r.(?) p.(=)
EXOC8 NM_175876.3 ?/. - c.62G>T r.(?) p.(Gly21Val)


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