Variant #0000129174 (NC_000023.10:g.(pter_78654)_(2694240_4300000)dup)

Individual ID 00080130
Chromosome X
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.(pter_78654)_(2694240_4300000)dup
DNA change (hg38) -
Published as arr[hg18] Xp22.33(18,654-2,704,240)x3 dn
ISCN arr[hg19] Xp22.33(78,654-2,694,240)x3 dn
DB-ID chrX_002748
Variant remarks -
Reference PubMed: Bruce 2009, PubMed: Fokstuen 2013, for EUCID-SRS consortium
ClinVar ID -
dbSNP ID -
Origin De novo
Segregation -
Frequency -
Re-site -
VIP -
Methylation normal methylation H19/IGF2:IG-DMR, KCNQ1OT1:TSS-DMR
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
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)




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000080224 DNA arrayCNV - - - 1 Zeynep Tümer


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