Variant #0001020920 (NC_000016.9:g.pter_3970809delins[NC_000017.10:g.pter_1277413])

Individual ID 00459554
Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.pter_3970809delins[NC_000017.10:g.pter_1277413]
DNA change (hg38) g.pter_3920808delins[NC_000017.11:g.pter_1374119]
Published as -
ISCN -
DB-ID chr16_006858
Variant remarks -
Reference -
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 Rikke Christensen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2025-01-14 18:17:37 +01:00 (CET)
Date last edited 2025-01-14 18:17:59 +01:00 (CET)




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000461180 DNA SEQ-NG Blood WGS - 2 Rikke Christensen


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