Variant #0000438429 (NC_000003.11:g.[NC_000012.11:52312101_qter]delins[G;pter_48252146inv])

Individual ID 00207502
Chromosome 3
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.[NC_000012.11:52312101_qter]delins[G;pter_48252146inv]
DNA change (hg38) -
Published as -
ISCN t(12,3)(q13,p21)
DB-ID chr3_004452
Variant remarks other translocation not described
Reference PubMed: Wooderchak-Donahue 2018
ClinVar ID -
dbSNP ID -
Origin DUPLICATE record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2018-11-23 17:41:00 +01:00 (CET)
Date last edited 2020-05-12 19:21:26 +02:00 (CEST)




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000208539 DNA;RNA RT-PCR;SEQ - WGS ACVRL1 2 Johan den Dunnen


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