Genomic variant #0000043061

Individual ID 00022077
Chromosome 11
Allele Parent #2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.32456394G>T
Reference -
DB-ID WT1_000033 See all 2 reported entries
dbSNP ID -
Variant remarks -
Genetic origin -
Segregation -
Also Known As -
Is Greek Founder -
Geographic Origin (for founder variants) -
Average frequency (large NGS studies) Retrieve
Average frequency in greek population 0.00034
Allele Count 2
Allele Number 5900
Owner Stevi Xera
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WT1 NM_000378.4 ./. - c.498C>A r.(=) p.(=)
WT1 NM_001198551.1 ./. - c.-4309C>A r.(=) p.(=)
WT1 NM_001198552.1 ./. - c.-4309C>A r.(=) p.(=)
WT1 NM_024424.3 ./. - c.498C>A r.(=) p.(=)
WT1 NM_024426.4 ./. - c.498C>A r.(=) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Type     

Genes screened     

Variants found     

Owner     
0000007575 DNA SEQ-NG-I 1 - 49 Stevi Xera