Variant #0000785903 (NC_000017.10:g.56772289C>T, NC_000017.10(NM_058216.1):c.146-3C>T (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.56772289C>T
DNA change (hg38) g.58694928C>T
Published as MCF-7 cell expression in vitro minigene splicing assay
ISCN -
DB-ID RAD51C_000240 See all 2 reported entries
Variant remarks -
Reference PubMed: Sanoguera-Miralles 2020
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2021-05-19 13:57:38 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
RAD51C NM_058216.1 -?/. - c.146-3C>T r.= p.= -


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