Variant #0000909042 (NC_000021.8:g.[NC_000013.9:g.(102944908_102954503)_qter]delins(47566752_47758267)_qter)

Individual ID 00428107
Chromosome 21
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.[NC_000013.9:g.(102944908_102954503)_qter]delins(47566752_47758267)_qter
DNA change (hg38) -
Published as hg18? chr13:101742909-101752504, chr21:46391180_46582695
ISCN 46,XY, t(13;21)(q32;q22.3)
DB-ID chr21_000892
Variant remarks -
Reference PubMed: Shimojima 2012
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 2022-12-21 17:56:55 +01:00 (CET)
Date last edited 2022-12-21 18:02:10 +01:00 (CET)




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000429519 DNA FISH;microscope - - - 4 Johan den Dunnen


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