Variant #0001018736 (NC_000005.9:g.(130600001_149800000)_qterdelins[NC_000023.10:g.(138000001_147100000)_qter])

Individual ID 00458185
Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.(130600001_149800000)_qterdelins[NC_000023.10:g.(138000001_147100000)_qter]
DNA change (hg38) g.(131200001_150400000)_qterdelins[NC_000023.11:g.(138900001_148000000)_qter]
Published as -
ISCN 46,XX,t(X;5)(q27;q31-q32)
DB-ID chr5_007321
Variant remarks -
Reference PubMed: Mossman 1983
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 2024-12-07 19:38:47 +01:00 (CET)
Date last edited N/A




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000459807 DNA microscope - - - 2 Johan den Dunnen


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