Genomic variant #0000042285

Individual ID 00022052
Chromosome 17
Allele Parent #2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.41251803T>C
Reference -
DB-ID BRCA1_000022 See all 13 reported entries
dbSNP ID rs56187033
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 0.00159
Allele Count 11
Allele Number 6936
Owner Stevi Xera
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BRCA1 NM_007294.3 ./. - c.536A>G r.(?) p.(Tyr179Cys)
BRCA1 NM_007297.3 ./. - c.395A>G r.(?) p.(Tyr132Cys)
BRCA1 NM_007298.3 ./. - c.536A>G r.(?) p.(Tyr179Cys)
BRCA1 NM_007299.3 ./. - c.536A>G r.(?) p.(Tyr179Cys)
BRCA1 NM_007300.3 ./. - c.536A>G r.(?) p.(Tyr179Cys)



Screenings


AscendingScreening ID     

Template     

Technique     

Type     

Genes screened     

Variants found     

Owner     
0000007549 DNA SEQ-NG-I 1 - 48 Stevi Xera