Variant #0000665603 (NC_000001.10:[NC_000022.10:g.(24792059_24798018)_qter]delins(151446793_151485910)_qter)

Individual ID 00029718
Chromosome 1
Allele Parent #1
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) [NC_000022.10:g.(24792059_24798018)_qter]delins(151446793_151485910)_qter
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr1_013715
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin DUPLICATE record
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 2020-05-10 14:33:32 +02:00 (CEST)
Date last edited 2020-05-10 14:36:07 +02:00 (CEST)




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000029765 DNA;RNA arrayCGH;FISH;PCR;RT-PCR;Southern - - - 4 Johan den Dunnen


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