All transcript variants in gene RAD51C

A Fanconi anemia mutation database.
Information The variants shown are described using the NM_058216.1 transcript reference sequence.

4 entries on 1 page. Showing entries 1 - 4.
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Effect     

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

Haplotype     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
-?/. 2 c.237T>G - r.(?) p.(=) - g.56772383T>G - - - RAD51C_000030 - - - - Germline ? 1/101 controls - 0 - Christine Rappaport
-?/. 2 c.237T>G - - p.= - g.56772383T>G - - - RAD51C_000030 DNA from FFPE tumor tissue: no LOH, no abnormal promotor methylation detected - - - In vitro (cloned) ? - - 0 - Christine Rappaport
-?/. 2 c.237T>G - r.(?) p.(=) - g.56772383T>G - - - RAD51C_000030 - - - - Germline ? 1/907 cases - 0 - Christine Rappaport
-?/. 2 c.237T>G - r.(?) p.(=) - g.56772383T>G - - - RAD51C_000030 not in 159 BRCA1/76 BRCA2 carriers - - - Germline ? 1/907 cases - 0 - Christine Rappaport
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