Variant #0000688853 (NC_000002.11:g.74154041G>T, NM_080916.1:c.4G>T (DGUOK))

Chromosome 2
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.74154041G>T
DNA change (hg38) -
Published as DGUOK(NM_080916.2):c.4G>T (p.A2S), DGUOK(NM_080916.3):c.4G>T (p.A2S)
ISCN -
DB-ID DGUOK_000012 See all 3 reported entries
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) 0.00254 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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DGUOK NM_080916.1 ?/. - c.4G>T r.(?) p.(Ala2Ser)


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