Variant #0000405142 (NC_000007.13:g.150235783A>G)

Individual ID 00180509
Chromosome 7
Allele Unknown
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.150235783A>G
DNA change (hg38) g.150538695A>G
Published as -
ISCN -
DB-ID chr7_003812
Variant remarks for details see the Uveogene database
Reference PubMed: Lee 2013
ClinVar ID -
dbSNP ID rs1522596
Origin Germline
Segregation -
Frequency 315/758 cases
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Peizeng Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2018-09-07 14:35:38 +02:00 (CEST)
Date last edited 2018-09-07 15:00:54 +02:00 (CEST)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000181446 DNA arraySNP Blood - GIMAP4 1 Peizeng Yang


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