Genomic variant #0000046734

Individual ID 00024214
Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.56798128A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID RAD51C_000016 See all 13 reported entries
Variant remarks not in 190 controls
Reference PubMed: Thompson 2012, Journal: Thompson 2012
ClinVar ID -
dbSNP ID rs28363317
Origin Unknown
Segregation ?
Frequency 3/267 cases
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.00784 View details
Owner Ian Campbell




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

Haplotype     
RAD51C NM_058216.1 ?/. 6 c.859A>G - r.(?) p.(Thr287Ala) -



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000024206 DNA SEQ - - RAD51C 8 Ian Campbell