Variant #0000763361 (NC_000003.11:g.47098509_48109065del)

Individual ID 00361744
Chromosome 3
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.47098509_48109065del
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr3_006814
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin De novo
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Davor Lessel
Database submission license No license selected
Created by Davor Lessel
Options




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

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Variants found     

Owner     
0000362972 DNA arraySNP - - - 1 Davor Lessel