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

Variant on transcripts

Stop! No entries in the database yet!


AscendingScreening ID     



Genes screened     

Variants found     

0000000100 DNA SEQ - 1 Johan den Dunnen