Variant #0000188344 (NC_000016.9:g.79245670C>T, WWOX(NM_016373.2):c.1222C>T)

Individual ID 00117031
Chromosome 16
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.79245670C>T
DNA change (hg38) g.79211773C>T
Published as -
ISCN -
DB-ID WWOX_000012
Variant remarks -
Reference PubMed: Bobbili 2018, Journal: Bobbili 2018
ClinVar ID -
dbSNP ID rs144234059
Origin Germline
Segregation -
Frequency 1/194 cases RE
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00011 View details
Owner Dheeraj Bobbili
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WWOX NM_016373.2 ./. - c.1222C>T r.(?) p.(Arg408Trp)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000117512 DNA SEQ-NG - - - 1 Dheeraj Bobbili