Product Details

SNP ID
rs2279856
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:143973176 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGTGCAGGGAGGCCGAGGGCGACCC[C/G]GCTGATGGAGAGTCTGCTCTTGTTA
Phenotype
MIM: 612200
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
C3orf58 PubMed Links

Gene Details

Gene
C3orf58
Gene Name
chromosome 3 open reading frame 58
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001134470.1 Intron NP_001127942.1
NM_173552.3 Intron NP_775823.1
XM_011512543.2 Intron XP_011510845.1
XM_017005869.1 Intron XP_016861358.1

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