Product Details

SNP ID

rs672636

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:127700158 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTAAATGAGAATTATTTAGACAAA[A/G]TTAATTATTTTCATGTAATGGGAGA

Phenotype

MIM: 613607

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

THEMIS PubMed Links

Additional Information

For this assay, SNP(s) [rs117689010] are located under a primer 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

THEMIS

Gene Name

thymocyte selection associated

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001010923.2		Intron			NP_001010923.1
NM_001164685.1		Intron			NP_001158157.1
NM_001164687.1		Intron			NP_001158159.1
NM_001318531.1		Intron			NP_001305460.1
XM_011535813.2		Intron			XP_011534115.1
XM_011535814.2		Intron			XP_011534116.1
XM_011535816.1		Intron			XP_011534118.1
XM_017010848.1		Intron			XP_016866337.1
XM_017010849.1		Intron			XP_016866338.1

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