Product Details

SNP ID
rs146552387
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:21444943 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACAGGTGGTGCGCGTGGGCAGGGCG[C/T]GGGGACATGGGGCCCGACATGGAGC
Phenotype
MIM: 607712
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
HIC2 PubMed Links

Gene Details

Gene
HIC2
Gene Name
hypermethylated in cancer 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_015094.2 181 Silent Mutation CGC,CGT R16R NP_055909.2
XM_011530007.2 181 Silent Mutation CGC,CGT R16R XP_011528309.1
XM_011530008.2 181 Silent Mutation CGC,CGT R16R XP_011528310.1
XM_011530009.2 181 Silent Mutation CGC,CGT R16R XP_011528311.1
XM_011530010.2 181 Silent Mutation CGC,CGT R16R XP_011528312.1
XM_017028669.1 181 UTR 5 XP_016884158.1

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