Variant #0000939711 (NC_000001.10:g.pter_73895578delins[GTAGA;NC_000006.11:g.157292080_qterinv])

Individual ID 00440287
Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic (dominant)
DNA change (genomic) (Relative to hg19 / GRCh37) g.pter_73895578delins[GTAGA;NC_000006.11:g.157292080_qterinv]
DNA change (hg38) -
Published as 46,XY,t(1;6)(p31;q25)dn
ISCN -
DB-ID chr1_015567
Variant remarks -
Reference PubMed: Halgren 2012
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 2023-10-31 19:48:08 +01:00 (CET)
Date last edited N/A




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000441772 DNA arrayCGH;microscope;PCR;SEQ - - - 4 Johan den Dunnen


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