Variant #0000078729 (NC_000008.10:g.(139900001_146364022)_qterdelins[NC_000023.10:pter_(32533500_32633500)inv])

Individual ID 00049892
Chromosome 8
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.(139900001_146364022)_qterdelins[NC_000023.10:pter_(32533500_32633500)inv]
DNA change (hg38) -
Published as -
ISCN t(X;8)(p21.1;q24.3)
DB-ID chr8_000000 See all 5 reported entries
Variant remarks translocation
Reference PubMed: Meitinger 1988, Journal: Meitinger 1988
ClinVar ID -
dbSNP ID -
Origin Germline/De novo (untested)
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 2015-09-14 15:44:41 +02:00 (CEST)
Date last edited 2020-05-12 19:21:26 +02:00 (CEST)




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000049813 DNA MIC;PFGE;Southern - - DMD 4 Johan den Dunnen


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