Product Details

SNP ID

rs6657647

Assay Type

Functionally tested

NCBI dbSNP Submissions

11

Location

Chr.1:150740297 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GAAACAATTCTAAGTGAATGGGGTA[C/T]GAAGGAGATAGTATTTGAGGCAGGA

Phenotype

MIM: 116845

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CTSS PubMed Links

Gene Details

Gene

CTSS

Gene Name

cathepsin S

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001199739.1		Intron			NP_001186668.1
NM_004079.4		Intron			NP_004070.3

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