Variant #0000000111 (NC_000001.10:g.230905413_230905423dup)

Individual ID 00000099
Chromosome 1
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.230905413_230905423dup
Marker/Name D1S1656
HGVS/Repeat g.230905352CA[5]CCTA[1]TCTA[14]TCA[1]TCTA[4]
Repeat CA[5]CCTA[1]TCTA[14]TCA[1]TCTA[4]
Published_as CE19.3 (TAGA)4(TGA)1(TAGA)14(TAGG)1(TG)5
Haplotype D1S1656-19.3[5-1-14-1-4]
dbSNP ID -
Reference Lareu 1998
DB-ID chr1_000014
Variant remarks -
Genetic origin Germline
Frequency 3/45 chromosomes
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Johan den Dunnen
Database submission license No license selected
Created by Johan den Dunnen
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Variant on transcripts

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Screenings


AscendingScreening ID     

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Owner     
0000000098 DNA SEQ - 1 Johan den Dunnen