Variant #0000000099 (NC_000001.10:g.230905362_230905389del)

Individual ID 00000087
Chromosome 1
Allele Parent #1
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
DNA change (genomic) (Relative to hg19 / GRCh37) g.230905362_230905389del
Marker/Name D1S1656
HGVS/Repeat g.230905352CA[5]TCTA[10]
Repeat CA[5]TCTA[10]
Published_as CE10 (TAGA)10(TG)5
Haplotype D1S1656-10[5-0-0-0-10]
dbSNP ID -
Reference Lareu 1998
DB-ID chr1_000002
Variant remarks -
Genetic origin Germline
Frequency 2/45 chromosomes
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license No license selected
Created by Johan den Dunnen
Date created 2016-07-11 10:30:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts

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Screenings


AscendingScreening ID     

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Technique     

Genes screened     

Variants found     

Owner     
0000000086 DNA SEQ - 1 Johan den Dunnen