Variant #0000460199 (NC_000005.9:g.(?_36666071)_(39426327_?)?)

Individual ID 00226087
Chromosome 5
Allele Both (homozygous)
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.(?_36666071)_(39426327_?)?
DNA change (hg38) g.(?_36665969)_(39426225_?)?
Published as -
ISCN 5p13.1-p13.2
DB-ID chr5_004428
Variant remarks mapped to homozygous region flanked by SNPs rs930072 and rs3812039
Reference Andres, under review 2019
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner M. Hashim Raza
Database submission license Creative Commons Attribution-NonCommercial 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2019-02-24 12:53:54 +01:00 (CET)
Date last edited 2019-02-24 12:58:08 +01:00 (CET)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

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Owner     
0000227154 DNA arraySNP - - - 1 M. Hashim Raza


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