Genomic variant #0000046672

Individual ID 00000032
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.56772383T>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID RAD51C_000030 See all 4 reported entries
Variant remarks DNA from FFPE tumor tissue: no LOH, no abnormal promotor methylation detected
Reference -
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation ?
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Christine Rappaport




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

Haplotype     
RAD51C NM_058216.1 -?/. 2 c.237T>G - - p.= -



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000024172 DNA MET;SEQ - - RAD51C 1 Christine Rappaport