Variant #0000129144 (NC_000017.10:g.(70900001_qter)delins[NC_000001.10:(185800001_198700000)_qter])

Individual ID 00080105
Chromosome 17
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.(70900001_qter)delins[NC_000001.10:(185800001_198700000)_qter]
DNA change (hg38) -
Published as -
ISCN 46,XY,t(1;17)(q31;q25)dn
DB-ID chr17_001702
Variant remarks translocation
Reference PubMed: Midro 1993, PubMed: Fokstuen 2013, for EUCID-SRS consortium
ClinVar ID -
dbSNP ID -
Origin De novo
Segregation -
Frequency -
Re-site -
VIP -
Methylation n/a
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Zeynep Tümer
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2016-09-01 17:30:25 +02:00 (CEST)
Date last edited 2020-10-01 16:53:33 +02:00 (CEST)




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

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Variants found     

Owner     
0000080197 DNA microscope - - - 4 Zeynep Tümer


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