Product Details

SNP ID
rs140424917
Assay Type
Functionally tested
NCBI dbSNP Submissions
3
Location
Chr.1:31423719 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGTCCTGCCTCTGCGGCTCTGCCCC[C/T]TGCATCCTGTGCAGCTGCTGCCCCG
Phenotype
MIM: 614549
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SERINC2 PubMed Links

Gene Details

Gene
SERINC2
Gene Name
serine incorporator 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001199037.1 1027 Silent Mutation CCC,CCT P26P NP_001185966.1
NM_001199038.1 1027 Silent Mutation CCC,CCT P31P NP_001185967.1
NM_001199039.1 1027 UTR 5 NP_001185968.1
NM_018565.3 1027 Silent Mutation CCC,CCT P26P NP_061035.2
NM_178865.4 1027 Silent Mutation CCC,CCT P22P NP_849196.2

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