Genomic variant #0000001902

Individual ID 00000009
Chromosome 1
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.209802870G>A
Reference dbSNP
DB-ID IRF6_000001 See all 8 reported entries
Frequency 0.356 Patients_Q37.5_left
Allele Count 42
Allele Number 118
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     
IRF6 NM_006147.3 ./. - c.-75-827C>T - r.(=) p.(=) -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000010 DNA TaqMan - 253 Admin