Product Details

SNP ID
rs192158165
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:96040351 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCAGAGCTGGCTCCAGGGAAGGGCT[A/G]CGTTTGGCCTGGGAGAGTAAGTCCC
Phenotype
Polymorphism
A/G, Transition 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_001252507.2 281 Intron NP_001239436.1
NM_001282463.1 281 Intron NP_001269392.1
NM_001282464.1 281 Intron NP_001269393.1
NM_001289139.1 281 Missense Mutation TAC,TGC Y35C NP_001276068.1
XM_017021469.1 281 Intron XP_016876958.1

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