Variant #0000000004 (NC_000001.10:g.230905352_230905429=)

Individual ID 00000007
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.230905352_230905429=
Marker/Name D1S1656
HGVS/Repeat g.230905352CA[5]CCTA[1]TCTC[16]
Repeat CA[5]CCTA[1]TCTC[16]
Published_as [TAGA]16TAGG[TG]5
Haplotype D1S1656-17
dbSNP ID -
Reference Parson 2016, Parson 2016
DB-ID chr1_000001
Variant remarks length capillary electrophoresis 17
Genetic origin Germline
Frequency -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Johan den Dunnen
Database submission license No license selected
Created by Johan den Dunnen
Date created 2016-06-20 09:16:54 +02:00 (CEST)
Date last edited 2016-06-27 11:04:13 +02:00 (CEST)




Variant on transcripts

Stop! No entries in the database yet!



Screenings


AscendingScreening ID     

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Genes screened     

Variants found     

Owner     
0000000006 DNA SEQ - 1 Johan den Dunnen