Product Details

SNP ID
rs145983648
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.15:89477569 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCGGAGGCCGCTGTCACAGCACCCA[C/T]GATGCCGCCTATGATGCCAGGAATG
Phenotype
MIM: 605381
Polymorphism
C/T, Transition 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 1129 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 1129 Missense Mutation ATG,GTG M354V NP_001307970.1
NM_016321.2 1129 Missense Mutation ATG,GTG M354V NP_057405.1

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