Product Details

Assay Reference Genome
Location

Chr.17:58711805 on build GRCh38
Cytoband
17q22
Species
Homo sapiens
Variation Type
Copy Number

Additional Information

Target Gene Details

Entrez Gene ID
5889
Gene Symbol
RAD51C
Gene Name
RAD51 paralog C
Gene Aliases
BROVCA3, FANCO, R51H3, RAD51L2
Location
Chr.17:58692538-58734342 on build GRCh38
Assay Gene Location
Within Intron 7
Gene Symbol Transcript Accession Exon Location Assay Location Protein ID
RAD51C NM_058216.2 NP_478123.1
NR_103872.1
XM_006722001.3 XP_006722064.1
XM_006722002.3 XP_006722065.1
XM_006722004.3 XP_006722067.1
XM_006722005.3 XP_006722068.1
XM_011525092.2 XP_011523394.1
XM_011525093.2 XP_011523395.1
XM_011525094.2 XP_011523396.1
XM_017024914.1 XP_016880403.1
XM_017024915.1 XP_016880404.1
XM_017024916.1 XP_016880405.1
XM_017024917.1 XP_016880406.1
XM_017024918.1 XP_016880407.1
XM_017024919.1 XP_016880408.1
AF029669.1 AAC39604.1
AK303363.1
BC107753.1 AAI07754.1

Target Copy Number Variation Details

DGV Version
Release date: 2016-05-15, GRCh GRCh38
Target
Variation
Location CNV
Subtype
Genes
nsv833498 Chr17:58652063 - 58815031 on Build GRCh38 Loss TEX14 PPM1E RAD51C
nsv428347 Chr17:58565015 - 58717588 on Build GRCh38 Gain TEX14 RAD51C

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