Variant #0000000113 (NC_000002.11:g.68239080_6823917=)

Individual ID 00000101
Chromosome 2
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.68239080_6823917=
Marker/Name D2S441
HGVS/Repeat g.68239080CTAT[12]
Repeat CTAT[12]
Published_as TCTA[12]
Haplotype D2S441-12
dbSNP ID -
Reference van der Gaag 2015
DB-ID chr2_000054
Variant remarks length capillary electrophoresis 12
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 2016-07-11 15:48:52 +02:00 (CEST)
Date last edited N/A




Variant on transcripts

Stop! No entries in the database yet!



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000100 DNA SEQ - 1 Johan den Dunnen