Genomic variant #0000046675

Individual ID 00000035
Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.56772284A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID RAD51C_000028 See all 2 reported entries
Variant remarks DNA from FFPE tumor tissue: no abnormal promotor methylation detected; RNA/cDNA: no abnormalities
Reference -
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation ?
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.00146 View details
Owner Christine Rappaport




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

Haplotype     
RAD51C NM_058216.1 -?/. 1i c.146-8A>G - - p.= -



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000024175 DNA;RNA MET;RT-PCR;SEQ - - RAD51C 1 Christine Rappaport