Genomic variant #0000026839

Individual ID 00020717
Chromosome 11
Allele Parent #2
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.32438008C>T
Reference -
DB-ID WT1_000021
dbSNP ID -
Variant remarks -
Genetic origin Germline
Segregation -
Also Known As -
Is Greek Founder -
Geographic Origin (for founder variants) -
Average frequency (large NGS studies) Variant not found in online data sets
Average frequency in greek population 0.00024
Owner Despoina Kalfakakou
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WT1 NM_000378.4 ?/? - c.950+1115G>A r.(=) p.(=)
WT1 NM_001198551.1 ?/? - c.365+28G>A r.(=) p.(=)
WT1 NM_001198552.1 ?/? - c.314+1115G>A r.(=) p.(=)
WT1 NM_024424.3 ?/? - c.1001+28G>A r.(=) p.(=)
WT1 NM_024426.4 ?/? - c.1001+28G>A r.(=) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Type     

Genes screened     

Variants found     

Owner     
0000001369 DNA SEQ-NG-I 1 - 15 Despoina Kalfakakou