Variant #0000442534 (NC_000001.10:g.(?_49580287)_(49672039_?)del)

Individual ID 00210051
Chromosome 1
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.(?_49580287)_(49672039_?)del
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr1_008129
Variant remarks -
Reference PubMed: Vadgama 2019, Journal: Vadgama 2019
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nirmal Vadgama
Database submission license No license selected
Created by Nirmal Vadgama
Date created 2018-12-26 03:24:13 +01:00 (CET)
Date last edited 2019-07-02 07:59:54 +02:00 (CEST)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

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Variants found     

Owner     
0000211109 DNA arrayCNV Buccal Microarray - 2 Nirmal Vadgama


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