Variant #0000000088 (NC_000002.11:g.218879547C>A)

Individual ID 00000038
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.218879547C>A
Marker/Name D2S1338
HGVS/Repeat -
Repeat -
Published_as -
Haplotype D2S1338-17[A-0-0-11-6]
dbSNP ID rs6736691
Reference vd Gaag, in press
DB-ID chr2_000003 See all 15 reported entries
Variant remarks -
Genetic origin Germline
Frequency -
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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Variants found     

Owner     
0000000037 DNA SEQ - 2 Johan den Dunnen