Variant #0000000035 (NC_000002.11:g.[218879593_218879602del;218879632_218879651del])

Individual ID 00000035
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.[218879593_218879602del;218879632_218879651del]
Marker/Name D2S1338
HGVS/Repeat g.218879582GGAA[10]GGCA[6]
Repeat GGAA[10]GGCA[6]
Published_as CE16-GGAA[10]GGCA[6]
Haplotype D2S1338-16[A-0-0-10-6]
dbSNP ID -
Reference vd Gaag, in press
DB-ID chr2_000006
Variant remarks -
Genetic origin Germline
Frequency 15/202 chromosomes
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 2016-06-27 13:14:31 +02:00 (CEST)
Date last edited 2016-06-27 22:09:21 +02:00 (CEST)




Variant on transcripts

Stop! No entries in the database yet!



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000034 DNA SEQ - 2 Johan den Dunnen