Product Details

SNP ID
rs9955058
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:68725408 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCTACTTCAGGTCACAAAAATCTAC[A/C]ATCAAGGCGTCAGAAGGCTCTGCTC
Phenotype
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
CCDC102B PubMed Links

Gene Details

Gene
CCDC102B
Gene Name
coiled-coil domain containing 102B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001093729.1 Intron NP_001087198.1
NM_024781.2 Intron NP_079057.2
XM_011526174.2 Intron XP_011524476.1
XM_011526175.2 Intron XP_011524477.1
XM_017025973.1 Intron XP_016881462.1
XM_017025974.1 Intron XP_016881463.1
XM_017025975.1 Intron XP_016881464.1
XM_017025976.1 Intron XP_016881465.1
XM_017025977.1 Intron XP_016881466.1
XM_017025978.1 Intron XP_016881467.1
XM_017025979.1 Intron XP_016881468.1
XM_017025980.1 Intron XP_016881469.1

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