Product Details

SNP ID
rs9533632
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.13:43822295 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTCGTGTTCTTTTCCCTCACTTTCC[C/G]GCAAATGGAGTCTGTCTCTGTCTGC
Phenotype
MIM: 613408
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
CCDC122 PubMed Links

Gene Details

Gene
CCDC122
Gene Name
coiled-coil domain containing 122
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_144974.3 1816 Intron NP_659411.2
XM_017020397.1 1816 Intron XP_016875886.1
XM_017020398.1 1816 Intron XP_016875887.1
XM_017020399.1 1816 UTR 3 XP_016875888.1

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