Product Details

SNP ID
rs139072089
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:79779411 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAACATCCTGGACCCGAGGCTGCTC[C/T]TGGCCTTCCAGAAGAAGTGAGGACG
Phenotype
MIM: 602770
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CBX2 PubMed Links

Gene Details

Gene
CBX2
Gene Name
chromobox 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_005189.2 224 Silent Mutation CTG,TTG L56L NP_005180.1
NM_032647.3 224 Silent Mutation CTG,TTG L56L NP_116036.1
XM_011525382.1 224 Silent Mutation CTG,TTG L56L XP_011523684.1
XM_011525383.2 224 UTR 5 XP_011523685.1

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