Product Details

SNP ID

rs187732111

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:33043849 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATCCAATGATTCTGAGGAAGGCCTC[A/G]AAGATGCTGTGGAAGGTGCTGATGA

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

TCP11L1 PubMed Links

Additional Information

For this assay, SNP(s) [rs1064005] 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

TCP11L1

Gene Name

t-complex 11 like 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145541.1	475	Missense Mutation	AAA,GAA	K26E	NP_001139013.1
NM_018393.3	475	Missense Mutation	AAA,GAA	K26E	NP_060863.3
XM_011520204.2	475	Missense Mutation	AAA,GAA	K26E	XP_011518506.1
XM_011520205.2	475	Missense Mutation	AAA,GAA	K26E	XP_011518507.1
XM_011520206.2	475	Missense Mutation	AAA,GAA	K26E	XP_011518508.1
XM_011520207.2	475	Missense Mutation	AAA,GAA	K26E	XP_011518509.1
XM_017017989.1	475	Missense Mutation	AAA,GAA	K26E	XP_016873478.1
XM_017017990.1	475	Missense Mutation	AAA,GAA	K26E	XP_016873479.1
XM_017017991.1	475	Intron			XP_016873480.1
XM_017017992.1	475	Intron			XP_016873481.1

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