View genomic variant #0000000954

Individual ID 00000138
Chromosome 5
Allele Unknown
Affects function (reported) Effect unknown
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.112841569C>T
Reference -
DB-ID APC_000014
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.5975C>T r.(?) p.(Pro1992Leu) Unknown no -



Screenings


AscendingScreening ID     

Template     

Technique     

Lab     

Remarks     

Date of test     

Type of test     

Genes screened     

Variants found     

Owner     
0000000149 DNA SEQ-NG Myriad myRisk® Hereditary Cancer Test 25-may-2017 - - 1 Lina Nuñez-Private Practice