Variant #0000764628 (NC_000023.10:g.pter_(24900001_37600000)delins[NC_000019.9:g.(39000000_44000000)_qterinv])

Individual ID 00362541
Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic (dominant)
DNA change (genomic) (Relative to hg19 / GRCh37) g.pter_(24900001_37600000)delins[NC_000019.9:g.(39000000_44000000)_qterinv]
DNA change (hg38) -
Published as -
ISCN 46,XX,t(X;19)(p21;q13)
DB-ID chrX_016894
Variant remarks -
Reference PubMed: Gustavsson 1997
ClinVar ID -
dbSNP ID -
Origin De novo
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 2021-04-22 15:25:48 +02:00 (CEST)
Date last edited 2021-04-22 15:30:19 +02:00 (CEST)




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Variants found     

Owner     
0000363769 DNA FISH;microscope - - RPS19 2 Johan den Dunnen


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