Variant #0000129141 (NC_000011.9:g.2018812_2024740|lom)

Individual ID 00080104
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.2018812_2024740|lom
DNA change (hg38) g.1997582_2003510|lom
Published as -
ISCN -
DB-ID chr11_000437 See all 7 reported entries
Variant remarks -
Reference PubMed: Cardarelli 2010, PubMed: Fokstuen 2013, for EUCID-SRS consortium
ClinVar ID -
dbSNP ID -
Origin Not applicable
Segregation -
Frequency -
Re-site -
VIP -
Methylation loss of methylation H19/IGF2:IG-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


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Owner     
0000080196 DNA ? - - - 2 Zeynep Tümer


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