Product Details

SNP ID
rs7147874
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:96042440 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGTAGAGGATAGAAGCTGGAGGGAT[G/T]CCTGGGGCTGGGCATGCATGCTTGT
Phenotype
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
C14orf132 PubMed Links

Gene Details

Gene
C14orf132
Gene Name
chromosome 14 open reading frame 132
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001252507.2 Intron NP_001239436.1
NM_001282463.1 Intron NP_001269392.1
NM_001282464.1 Intron NP_001269393.1
NM_001289139.1 Intron NP_001276068.1
XM_017021469.1 Intron XP_016876958.1

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