Variant #0000000005 (NC_000002.11:g.218879582_218879673=)

Individual ID 00000008
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.218879582_218879673=
Marker/Name D2S1338
HGVS/Repeat g.218879582GGAA[2]GGAC[1]GGAA[13]GGCA[7]
Repeat GGAA[2]GGAC[1]GGAA[13]GGCA[7]
Published_as TGCC[7]TTCC[13]GTCC[1]TTCC[2]
Haplotype D2S1338-23
dbSNP ID -
Reference Parson 2016, Parson 2016
DB-ID chr2_000001 See all 2 reported entries
Variant remarks length capillary electrophoresis 23
Genetic origin Germline
Frequency -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Jamie Zeegers
Database submission license No license selected
Created by Jamie Zeegers

Variant on transcripts

Stop! No entries in the database yet!


AscendingScreening ID     



Genes screened     

Variants found     

0000000007 DNA SEQ - 1 Jamie Zeegers