Product Details

SNP ID

rs149302250

Assay Type

Functionally Tested

NCBI dbSNP Submissions

3

Location

Chr.1:27879833 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTGTGGTGATGCACCTCGGGATCC[A/G]CTCTGCCCGCTGTGTCCTGGGCATG

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

THEMIS2 PubMed Links

Additional Information

For this assay, SNP(s) [rs78644103] 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

THEMIS2

Gene Name

thymocyte selection associated family member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001039477.2	454	Intron			NP_001034566.1
NM_001105556.2	454	Missense Mutation	CAC,CGC	H142R	NP_001099026.1
NM_001286113.1	454	Missense Mutation	CAC,CGC	H142R	NP_001273042.1
NM_001286115.1	454	Missense Mutation	CAC,CGC	H142R	NP_001273044.1
NM_004848.3	454	Missense Mutation	CAC,CGC	H142R	NP_004839.2
XM_005246041.3	454	Intron			XP_005246098.1
XM_006711050.1	454	Missense Mutation	CAC,CGC	H142R	XP_006711113.1
XM_011542445.2	454	Missense Mutation	CAC,CGC	H95R	XP_011540747.1

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