Product Details

Assay Reference Genome
Location

Chr.17:58692646 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 Exon 1
Gene Symbol Transcript Accession Exon Location Assay Location Protein ID
RAD51C NM_002876.3 1 74 NP_002867.1
NM_058216.2 1 74 NP_478123.1
NR_103872.1 1 74
NR_103873.1
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_017024914.1 XP_016880403.1
XM_017024916.1 XP_016880405.1
XM_017024917.1 XP_016880406.1
AA304618.1
AF029669.1 AAC39604.1
AF029670.1 AAC39605.1
AI424321.1
AK129738.1
AK290487.1
AK303363.1
BC093930.1 AAH93930.1
BC101485.1 AAI01486.1
BC107753.1 1 78 AAI07754.1
BT007339.1 AAP36003.1

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 RAD51C PPM1E
nsv1066945 Chr17:58650965 - 58704810 on Build GRCh38 Loss TEX14 RAD51C
nsv428347 Chr17:58565015 - 58717588 on Build GRCh38 Gain TEX14 RAD51C

View Full Product Details