Product Details

SNP ID
rs458361
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:21444062 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GCACCCGCTCAGAACCCCATGTCTT[G/C]CTGCTGCATAAGCAGGAACACACCT
Phenotype
MIM: 607712
Polymorphism
G/C, Transversion 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 Intron NP_055909.2
XM_011530007.2 Intron XP_011528309.1
XM_011530008.2 Intron XP_011528310.1
XM_011530009.2 Intron XP_011528311.1
XM_011530010.2 Intron XP_011528312.1
XM_017028669.1 Intron XP_016884158.1

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