Variant #0000188649 (NC_000016.9:g.[chr16:(88700000_qter)delinschr11:(pter_12700000)inv])

Individual ID 00117219
Chromosome 16
Allele Maternal (confirmed)
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.[chr16:(88700000_qter)delinschr11:(pter_12700000)inv]
DNA change (hg38) -
Published as -
ISCN 46,XX,der(16)t(11;16)(p15.3;q24.3)mat
DB-ID chr16_000467 See all 2 reported entries
Variant remarks unbalanced translocation
Reference PubMed: Nakashima 2015, for EUCID-SRS consortium
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Zeynep Tümer
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2017-08-15 16:52:29 +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     
0000117681 DNA arrayCGH;microsat - - - 2 Zeynep Tümer


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