Variant #0000546362 (NC_000012.11:g.109535549C>T, NM_080911.2:c.65C>T (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.109535549C>T
DNA change (hg38) g.109097744C>T
Published as UNG(NM_080911.1):c.65C>T (p.P22L)
ISCN -
DB-ID ALKBH2_000001
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALKBH2 NM_001001655.2 -?/. - c.-4499G>A r.(?) p.(=)
UNG NM_080911.2 -?/. - c.65C>T r.(?) p.(Pro22Leu)


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