Product Details

SNP ID
rs146068597
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:129290708 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTCTGGGAAAGGGAAGACGCTGTGT[C/T]GTTTTAGCAGATGGATTCTATGAGT
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
HMCES PubMed Links

Gene Details

Gene
HMCES
Gene Name
5-hydroxymethylcytosine (hmC) binding, ES cell-specific
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001006109.1 462 Silent Mutation GTC,GTT V119V NP_001006109.1
NM_020187.2 462 Silent Mutation GTC,GTT V119V NP_064572.2
XM_005247636.3 462 Silent Mutation GTC,GTT V119V XP_005247693.1
XM_005247637.3 462 Intron XP_005247694.1
XM_017006877.1 462 Silent Mutation GTC,GTT V119V XP_016862366.1

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