Genomic variant #0000046708

Individual ID 00024207
Chromosome 17
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.56770097delG
DNA change (hg38) -
Published as -
ISCN -
DB-ID RAD51C_000048
Variant remarks -
Reference PubMed: Pelttari 2011
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation ?
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Johan den Dunnen




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

Haplotype     
RAD51C NM_058216.1 +/. 1 c.93delG - r.(?) p.fs -



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000024199 DNA PCR;SEQ - - RAD51C 1 Johan den Dunnen