Product Details

Assay Reference Genome
Location

Chr.1:243316865 on build GRCh38
Cytoband
1q43
Species
Homo sapiens
Variation Type
Copy Number

Additional Information

Target Gene Details

Entrez Gene ID
10806
Gene Symbol
SDCCAG8
Gene Name
serologically defined colon cancer antigen 8
Gene Aliases
BBS16, CCCAP, CCCAP SLSN7, HSPC085, NPHP10, NY-CO-8, SLSN7, hCCCAP
Location
Chr.1:243255328-243500092 on build GRCh38
Assay Gene Location
Overlaps Exon 13 - Intron 13
Gene Symbol Transcript Accession Exon Location Assay Location Protein ID
SDCCAG8 NM_006642.3 NP_006633.1
XM_005273013.4 XP_005273070.1
XM_005273018.1 XP_005273075.1
XM_005273021.4 XP_005273078.1
XM_005273022.3 XP_005273079.1
XM_005273023.4 XP_005273080.1
XM_006711727.3 XP_006711790.1
XM_006711728.3 XP_006711791.1
XM_011544021.2 XP_011542323.1
XM_011544022.2 XP_011542324.1
XM_011544023.2 XP_011542325.1
XM_011544024.2 XP_011542326.1
XM_011544026.2 XP_011542328.1
XM_011544028.2 XP_011542330.1
XM_011544029.2 XP_011542331.1
XM_011544030.2 XP_011542332.1
XM_017000103.1 XP_016855592.1
XM_017000104.1 XP_016855593.1
XM_017000105.1 XP_016855594.1
XM_017000106.1 XP_016855595.1
XM_017000107.1 XP_016855596.1
XM_017000108.1 XP_016855597.1
XM_017000109.1 XP_016855598.1
AF039690.1 AAC18039.1
AF161348.1 AAF28908.1
AF250731.1 AAO27830.1
AK297105.1
AK299212.1
AK299249.1
BC032454.1 AAH32454.1

Target Copy Number Variation Details

DGV Version
Release date: 2016-05-15, GRCh GRCh38
Target
Variation
Location CNV
Subtype
Genes
nsv1001488 Chr1:243227523 - 243419972 on Build GRCh38 Loss CEP170 MIR4677 SDCCAG8
nsv517939 Chr1:243213455 - 243359604 on Build GRCh38 Gain CEP170 MIR4677 SDCCAG8

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