Product Details

SNP ID

rs17682

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:3189269 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACACGAGTCACCTCCAAAGAGCTGC[A/G]ACTGTTTGAGAATCTGCCAAGAGGA

Phenotype

MIM: 608998

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

TSSC1 PubMed Links

Additional Information

For this assay, SNP(s) [rs57607506] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

TSSC1

Gene Name

tumor suppressing subtransferable candidate 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_006711893.2	1327	UTR 3			XP_006711956.1
XM_011510383.2	1327	UTR 3			XP_011508685.1
XM_011510384.2	1327	UTR 3			XP_011508686.1
XM_011510385.2	1327	UTR 3			XP_011508687.1
XM_011510387.2	1327	UTR 3			XP_011508689.1
XM_017004818.1	1327	UTR 3			XP_016860307.1

View Full Product Details