Variant #0000129103 (NC_000011.9:g.2018812_2024740|lom)

Individual ID 00080088
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 only H19 affected
Reference PubMed: Begemann 2012, PubMed: Eggermann 2014, PubMed: Brown 2014, for EUCID-SRS consortium
ClinVar ID -
dbSNP ID -
Origin Somatic
Segregation -
Frequency -
Re-site -
VIP -
Methylation loss of methylation H19/IGF2:IG-DMR, normal 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


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Owner     
0000080171 DNA MLPA-ms; PEms - methylation-sensitive single-nucleotide primer extension - 1 Zeynep Tümer


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