Variant #0000172302 (NC_000019.9:g.41511803C>G)

Individual ID 00106143
Chromosome 19
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.41511803C>G
DNA change (hg38) g.41005898C>G
Published as 14593C>G
ISCN -
DB-ID CYP2B6_000002
Variant remarks reference allele CYP2B6*1C
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2015-02-03 22:33:52 +01:00 (CET)
Date last edited N/A
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000106613 DNA SEQ - - CYP2B6 3 Johan den Dunnen


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