Variant #0000129161 (NC_000017.10:g.(pter_1512910)_(2312362_3300000)del)

Individual ID 00080119
Chromosome 17
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_1512910)_(2312362_3300000)del
DNA change (hg38) -
Published as -
ISCN arr[hg19] 17p13.3(1,512,910-2,312,362)x1 dn
DB-ID chr17_001692
Variant remarks deletion affecting 20 RefSeq genes
Reference PubMed: Spengler 2012, PubMed: Fokstuen2013, 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


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000080212 DNA microscope; arrayCNV; FISH; PCRq - - - 1 Zeynep Tümer


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.