Product Details

SNP ID
rs2072693
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:89471714 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GTAGCTTCTCCTTCTCCATTCTCAG[G/T]CAGACCCCCTGGGATGAAGGGGAGG
Phenotype
MIM: 605381
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
LOC105371031 PubMed Links

Gene Details

Gene
LOC105371031
Gene Name
translation initiation factor IF-2-like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
XM_017022800.1 1675 Intron XP_016878289.1
Gene
RHCG
Gene Name
Rh family C glycoprotein
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001321041.1 1675 UTR 3 NP_001307970.1
NM_016321.2 1675 UTR 3 NP_057405.1

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