Variant #0000185995 (NC_000023.10:g.?)

Individual ID 00115130
Chromosome X
Allele Maternal (confirmed)
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.?
DNA change (hg38) -
Published as -
ISCN -
DB-ID SHOX_000233 See all 19 reported entries
Variant remarks pseudoautosomal microdeletion involving SHOX, 1/5 patients
Reference PubMed: Zinn 2002, OMIM:var0003
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 Ralph Roeth
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Ralph Roeth
Date created 2006-12-13 14:29:32 +01:00 (CET)
Date last edited 2017-08-09 14:14:35 +02:00 (CEST)




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000115587 DNA FISH - - SHOX 2 Ralph Roeth


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