Product Details

SNP ID
rs1570638
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.9:72052854 on Build GRCh38
Set Membership
HapMap Validated
Context Sequence [VIC/FAM]
GTTAAGGGCCTCTCAGAAATGGAGG[C/T]GTATGTATGACCTCACTTAATTCCT
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
C9orf57 PubMed Links

Gene Details

Gene
C9orf57
Gene Name
chromosome 9 open reading frame 57
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001128618.1 Intron NP_001122090.1
XM_011518225.2 Intron XP_011516527.1

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