Product Details

SNP ID
rs115875756
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:231791726 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGTCTGTGGTGAACTTTTTTTTTCC[C/T]CTTCAGCTTGCGGAAGGAGCTAATG
Phenotype
MIM: 616010
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
COPS7B PubMed Links

Gene Details

Gene
COPS7B
Gene Name
COP9 signalosome subunit 7B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001282949.2 Intron NP_001269878.1
NM_001282950.2 Intron NP_001269879.1
NM_001282951.2 Intron NP_001269880.1
NM_001282952.2 Intron NP_001269881.1
NM_001308381.1 Intron NP_001295310.1
NM_022730.3 Intron NP_073567.1
XM_006712693.1 Intron XP_006712756.1
XM_011511638.1 Intron XP_011509940.1
XM_011511639.1 Intron XP_011509941.1
XM_011511640.1 Intron XP_011509942.1
XM_017004716.1 Intron XP_016860205.1
XM_017004717.1 Intron XP_016860206.1

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