Product Details

SNP ID
rs10162186
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.13:102729495 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GTAAGGGACCCCGAGAGCGACCCCA[A/G]CAACTTTTTGGAGGAACTCCATATA
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CCDC168 PubMed Links

Gene Details

Gene
CCDC168
Gene Name
coiled-coil domain containing 168
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001146197.1 21342 Silent Mutation CTG,TTG L7068L NP_001139669.1
XM_011521106.1 21342 Silent Mutation CTG,TTG L7028L XP_011519408.1

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