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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