Variant #0000546363 (NC_000012.11:g.109536287G>A, NM_080911.2:c.183G>A (UNG))

Chromosome 12
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.109536287G>A
DNA change (hg38) g.109098482G>A
Published as UNG(NM_003362.3):c.156G>A (p.P52=), UNG(NM_003362.4):c.156G>A (p.P52=)
ISCN -
DB-ID ALKBH2_000002 See all 2 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) 0.00053 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 2019-07-18 18:22:55 +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     
ALKBH2 NM_001001655.2 -?/. - c.-5237C>T r.(?) p.(=)
UNG NM_080911.2 -?/. - c.183G>A r.(?) p.(Pro61=)


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