Variant #0000459015 (NC_000024.9:g.(24070914_24639666)_(24876071_25505070)del)

Individual ID 00225595
Chromosome Y
Allele Paternal (inferred)
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.(24070914_24639666)_(24876071_25505070)del
DNA change (hg38) -
Published as -
ISCN -
DB-ID chrY_000133
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Csilla Gabriella Krausz
Database submission license No license selected
Created by Csilla Gabriella Krausz
Date created 2019-02-18 17:02:45 +01:00 (CET)
Date last edited 2019-02-18 22:08:55 +01:00 (CET)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000226674 DNA PCRdig - - CDY1, CDY1B, CDY2A, CDY2B, DAZ1, DAZ2, DAZ3, DAZ4, DAZL 1 Csilla Gabriella Krausz


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