Variant #0000461228 (NC_000024.9:g.(23978074_24354700)_(25316178_25505734)del)

Individual ID 00226112
Chromosome Y
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.(23978074_24354700)_(25316178_25505734)del
DNA change (hg38) -
Published as b1/b3 deletion
ISCN -
DB-ID chrY_000135
Variant remarks sY142+, sY1196_sY1189del, sY254+
Reference Moreno-Mendoza, submitted
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation ?
Frequency 1/497
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Elena Casamonti
Database submission license No license selected
Created by Elena Casamonti
Date created 2019-02-26 20:11:41 +01:00 (CET)
Date last edited 2019-02-27 15:33:59 +01:00 (CET)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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0000227184 DNA PCRm - sY142+, sY1196_sY1189del, sY254+ CDY1, CDY1B, DAZ1, DAZ2, DAZ3, DAZ4 1 Elena Casamonti


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