Variant #0000170294 (NC_000002.11:g.219892666G>T)

Individual ID 00104566
Chromosome 2
Allele Paternal (confirmed)
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.219892666G>T
DNA change (hg38) g.219027944G>T
Published as -
ISCN -
DB-ID chr2_000976
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Karine Poirier
Database submission license No license selected
Created by Karine Poirier
Date created 2017-05-15 12:43:45 +02:00 (CEST)
Date last edited 2017-05-16 17:41:33 +02:00 (CEST)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000105038 DNA;RNA RT-PCR;SEQ;SEQ-NG - - BMP15, CSNK2B, GPR144, HEPH, PLXNA3 8 Karine Poirier