Genomic variant #0000043638

Individual ID 00022095
Chromosome 13
Allele Parent #2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.32972626A>T
Reference -
DB-ID BRCA2_000018 See all 46 reported entries
dbSNP ID rs11571833
Variant remarks -
Genetic origin -
Segregation -
Also Known As -
Is Greek Founder -
Geographic Origin (for founder variants) -
Average frequency (large NGS studies) Retrieve
Average frequency in greek population 0.00695
Allele Count 46
Allele Number 6618
Owner Stevi Xera
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BRCA2 NM_000059.3 ./. - c.9976A>T r.(?) p.(Lys3326*)



Screenings


AscendingScreening ID     

Template     

Technique     

Type     

Genes screened     

Variants found     

Owner     
0000007593 DNA SEQ-NG-I 1 - 43 Stevi Xera