Product Details

SNP ID

rs10982497

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.9:115022769 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TAAAACAGGCATGAAAAACCACATC[C/T]TAATTCCTGCACAGGGTAAAAATGA

Phenotype

MIM: 187380

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

TNC PubMed Links

Additional Information

For this assay, SNP(s) [rs79929258] 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

TNC

Gene Name

tenascin C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002160.3		Intron			NP_002151.2
XM_005251972.3		Intron			XP_005252029.1
XM_005251973.3		Intron			XP_005252030.1
XM_005251974.3		Intron			XP_005252031.1
XM_005251975.3		Intron			XP_005252032.1
XM_006717096.3		Intron			XP_006717159.1
XM_006717097.3		Intron			XP_006717160.1
XM_006717098.3		Intron			XP_006717161.1
XM_006717101.3		Intron			XP_006717164.1
XM_011518625.2		Intron			XP_011516927.1
XM_011518626.2		Intron			XP_011516928.1
XM_011518628.2		Intron			XP_011516930.1
XM_011518629.2		Intron			XP_011516931.1
XM_017014678.1		Intron			XP_016870167.1
XM_017014679.1		Intron			XP_016870168.1
XM_017014680.1		Intron			XP_016870169.1
XM_017014681.1		Intron			XP_016870170.1

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