View genomic variant #0000006405

Individual ID 00000990
Chromosome 5
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.112839514T>A
Reference Risk factor
DB-ID APC_000032 See all 2 reported entries
Average frequency (large NGS studies) Variant not found in online data sets
Owner Lina Nuñez-Private Practice




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Zygosity     

Co_ocurrence     

Reference     
APC NM_000038.5 ./. 16 c.3920T>A r.(?) p.(Ile1307Lys) Homo no -



Screenings


AscendingScreening ID     

Template     

Technique     

Lab     

Remarks     

Date of test     

Type of test     

Genes screened     

Variants found     

Owner     
0000001192 DNA CNV;SEQ-NG Color-Genos Hereditary Cancer Risk Test (30 genes) 24-jul-2019 Multigenetic panel - 1 Lina Nuñez-Private Practice