Genomic variant #0000000984

Individual ID 00000004
Chromosome 11
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.76193093G>A
Reference dbSNP
DB-ID WNT11_000005 See all 7 reported entries
Frequency 0.250 Patients_Q37.2
Allele Count 1
Allele Number 4
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     
WNT11 NM_004626.2 ./. - c.598-1237C>T - r.(=) p.(=) -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000005 DNA TaqMan - 174 Admin