Product Details

SNP ID
rs201609791
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:21445048 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTTCCTGTGTGACGTCATCATCAT[G/T]GTGGAGAACTCCATCTTCCGGGCCC
Phenotype
MIM: 607712
Polymorphism
G/T, 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_015094.2 286 Missense Mutation ATG,ATT M51I NP_055909.2
XM_011530007.2 286 Missense Mutation ATG,ATT M51I XP_011528309.1
XM_011530008.2 286 Missense Mutation ATG,ATT M51I XP_011528310.1
XM_011530009.2 286 Missense Mutation ATG,ATT M51I XP_011528311.1
XM_011530010.2 286 Missense Mutation ATG,ATT M51I XP_011528312.1
XM_017028669.1 286 Missense Mutation ATG,ATT M33I XP_016884158.1

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