Variant #0000000580 (NC_000002.11:g.1493425_1493456=)

Individual ID 00000466
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.1493425_1493456=
Marker/Name TPOX
HGVS/Repeat g.1493423AATG[8]
Repeat AATG[8]
Published_as CE8-TGAA[8]
Haplotype TPOX-8 [C-CG-G-8]
dbSNP ID -
Reference van der Gaag 2016
DB-ID chr2_000055
Variant remarks -
Genetic origin Germline
Frequency -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Pieter Klap
Database submission license No license selected
Created by Pieter Klap




Variant on transcripts

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Screenings


AscendingScreening ID     

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Technique     

Genes screened     

Variants found     

Owner     
0000000465 DNA SEQ - 1 Pieter Klap