Product Details

SNP ID
rs140733152
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:96390901 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGAGGAATTGGACAGGGCAATGCT[A/G]GAATGGTTCAACCAGCAAAGAGCAA
Phenotype
MIM: 603211
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CCDC82 PubMed Links

Gene Details

Gene
CCDC82
Gene Name
coiled-coil domain containing 82
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001318736.1 908 Intron NP_001305665.1
NM_001318737.1 908 Intron NP_001305666.1
NM_024725.3 908 Intron NP_079001.2
XM_005274292.3 908 Intron XP_005274349.1
XM_006718911.3 908 Intron XP_006718974.1
XM_011542984.2 908 Intron XP_011541286.1
XM_011542987.2 908 Intron XP_011541289.1
XM_011542988.2 908 Intron XP_011541290.1
XM_017018305.1 908 Intron XP_016873794.1
XM_017018306.1 908 Intron XP_016873795.1
XM_017018307.1 908 Intron XP_016873796.1
XM_017018308.1 908 Intron XP_016873797.1
XM_017018309.1 908 Intron XP_016873798.1
XM_017018310.1 908 Intron XP_016873799.1
XM_017018311.1 908 Intron XP_016873800.1
XM_017018312.1 908 Intron XP_016873801.1
Gene
JRKL
Gene Name
JRK-like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001261833.1 908 Silent Mutation CTA,CTG L84L NP_001248762.1
NM_003772.3 908 Silent Mutation CTA,CTG L84L NP_003763.2

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