Variant #0000129096 (NC_000011.9:g.2719948_2722259|gom)

Individual ID 00080085
Chromosome 11
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.2719948_2722259|gom
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr11_000438 See all 10 reported entries
Variant remarks -
Reference PubMed: Bliek 2009, PubMed: Begemann 2012, PubMed: Fokstuen 2013, PubMed: Brown 2014, for EUCID-SRS consortium
ClinVar ID -
dbSNP ID -
Origin Somatic
Segregation -
Frequency -
Re-site -
VIP -
Methylation gain of methylation KCNQ1OT1:TSS-DMR
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Zeynep Tümer
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2016-09-01 17:30:25 +02:00 (CEST)
Date last edited 2020-10-01 16:53:33 +02:00 (CEST)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

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Genes screened     

Variants found     

Owner     
0000080165 DNA MCA; MLPA - - - 2 Zeynep Tümer


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