Variant #0000404984 (NC_000023.10:g.(102700000_102716771)_(102760337_102780000)[2])

Individual ID 00180302
Chromosome X
Allele Maternal (confirmed)
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.(102700000_102716771)_(102760337_102780000)[2]
DNA change (hg38) -
Published as -
ISCN hg19 arr(102716771–102760337)x2
DB-ID chrX_010576
Variant remarks 43 kb duplication
Reference PubMed: Martínez-Montero 2013, Journal: Martínez-Montero 2013
ClinVar ID -
dbSNP ID -
Origin Germline
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 2018-09-05 16:45:11 +02:00 (CEST)
Date last edited N/A




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

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Owner     
0000181239 DNA arrayCGH peripheral blood leucocytes - PLP1 3 Jesus Molano Mateos


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