Variant #0000046675 (NC_000017.10:g.56772284A>G, NC_000017.10(NM_058216.1):c.146-8A>G (RAD51C))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.56772284A>G
DNA change (hg38) g.58694923A>G
Published as -
ISCN -
DB-ID RAD51C_000028 See all 7 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 -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00122 View details
Owner Christine Rappaport
Database submission license No license selected
Created by Christine Rappaport
Date created 2014-11-02 12:02:12 +01:00 (CET)
Date last edited 2020-07-14 21:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

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


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