Variant #0000629393 (NC_000022.10:g.21433935_qterdelins[NC_000020.10:g.59970004_qter])

Individual ID 00274230
Chromosome 22
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.21433935_qterdelins[NC_000020.10:g.59970004_qter]
DNA change (hg38) -
Published as chr22:g.21433934::chr20:g.59970004
ISCN 46,XY,t(20;22)(q13.3;q11.2)
DB-ID chr22_002812
Variant remarks -
Reference PubMed: Schilit 2020, Journal: Schilit 2020
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 2019-12-26 14:29:26 +01:00 (CET)
Date last edited N/A




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000275389 DNA microscope;SEQ - - SYCP2 4 Johan den Dunnen


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