Product Details

SNP ID
rs78476902
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.19:1453309 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGCCCGAGTGCTGGTGTCCTCGGG[A/G]CAGACGGAGGTGCTGGAGCAGCTGA
Phenotype
MIM: 612034
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
APC2 PubMed Links

Gene Details

Gene
APC2
Gene Name
APC2, WNT signaling pathway regulator
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_005883.2 556 Silent Mutation GGA,GGG G68G NP_005874.1
XM_005259475.2 556 Silent Mutation GGA,GGG G92G XP_005259532.1
XM_006722607.2 556 Silent Mutation GGA,GGG G92G XP_006722670.1
XM_006722608.3 556 Silent Mutation GGA,GGG G169G XP_006722671.2
XM_006722609.3 556 Silent Mutation GGA,GGG G68G XP_006722672.1
XM_006722610.3 556 Silent Mutation GGA,GGG G169G XP_006722673.2

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