Variant #0000844859 (NC_000011.9:g.125889526C>T)

Individual ID 00406740
Chromosome 11
Allele Parent #1
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.125889526C>T
DNA change (hg38) g.126019631C>T
Published as Glu162Lys
ISCN -
DB-ID CDON_000010 See all 5 reported entries
Variant remarks -
Reference PubMed: Drissi 2022
ClinVar ID -
dbSNP ID rs3740909
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.10864 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-04-04 18:08:20 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000407987 DNA SEQ;SEQ-NG - - - 8 Johan den Dunnen


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