Variant #0000050412 (NC_000014.8:g.101179660_101179695TG[9])

Individual ID 00027198
Chromosome 14
Allele Maternal (confirmed)
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.101179660_101179695TG[9]
DNA change (hg38) -
Published as D14S1006:126
ISCN -
DB-ID chr14_000129
Variant remarks haplotype analysis shows biparental inheritance (D14S80-98, D14S608-197, D14S588-130, D14S1000-126, D14S617-143, D14S985-129, D14S1010-144, D14S292-108)
Reference PubMed: Kagami 2014
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2014-12-29 17:00:06 +01:00 (CET)
Date last edited 2019-08-17 12:37:01 +02:00 (CEST)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000027214 DNA PAGE;PCR leukocytes - - 2 Johan den Dunnen


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