Product Details

SNP ID
rs1890870
Assay Type
Functionally tested
NCBI dbSNP Submissions
22
Location
Chr.1:207018728 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GGAGGCTGAATTTGAGCCAGATCTA[C/T]ATGCTCCATCATCACTCTCCTGGGG
Phenotype
MIM: 611680
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
C1orf116 PubMed Links

Gene Details

Gene
C1orf116
Gene Name
chromosome 1 open reading frame 116
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001083924.1 4965 UTR 3 NP_001077393.1
NM_023938.5 4965 UTR 3 NP_076427.2
XM_005273259.1 4965 UTR 3 XP_005273316.1
XM_006711530.1 4965 UTR 3 XP_006711593.1
XM_011509973.2 4965 UTR 3 XP_011508275.1

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