Variant #0000460209 (NC_000002.11:g.(?_111705738)_(133160621_?)?)

Individual ID 00224974
Chromosome 2
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.(?_111705738)_(133160621_?)?
DNA change (hg38) g.(?_110948161_(132403048_?)?
Published as -
ISCN 2q13-q21.2
DB-ID chr2_009514
Variant remarks mapped to homozygous region flanked by SNPs rs729386 to rs2872920
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 13:50:40 +01:00 (CET)
Date last edited N/A
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

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Owner     
0000226052 DNA arraySNP - - - 2 M. Hashim Raza


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