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
Date created 2016-06-27 09:36:39 +02:00 (CEST)
Date last edited N/A




Variant on transcripts

Stop! No entries in the database yet!



Screenings


AscendingScreening ID     

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Technique     

Genes screened     

Variants found     

Owner     
0000000007 DNA SEQ - 1 Jamie Zeegers