Variant #0000129169 (NC_000007.13:g.?|gom)

Individual ID 00080125
Chromosome 7
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.?|gom
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr7_000000 See all 9 reported entries
Variant remarks -
Reference for EUCID-SRS consortium
ClinVar ID -
dbSNP ID -
Origin Somatic
Segregation -
Frequency -
Re-site -
VIP -
Methylation gain of methylation GRB10:alt-TSS-DMR, normal methylation H19/IGF2:IG-DMR, 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 16:54:17 +02:00 (CEST)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000080219 DNA MLPA-ms ; PEms - methylation-sensitive single-nucleotide primer extension - 1 Zeynep Tümer


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