Product Details

SNP ID
rs605468
Assay Type
Functionally Tested
NCBI dbSNP Submissions
50
Location
Chr.1:23384312 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CCTTATGCGGGCGAGGTATGTGGAT[A/G]ACAGGGAAGGGGGAAATACATAAAC
Phenotype
MIM: 604128
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
TCEA3 PubMed Links
Additional Information
For this assay, SNP(s) [rs74440078] 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
TCEA3
Gene Name
transcription elongation factor A3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_003196.2 Intron NP_003187.1
XM_006710864.1 Intron XP_006710927.1
XM_011542053.2 Intron XP_011540355.1
XM_017002200.1 Intron XP_016857689.1
XM_017002201.1 Intron XP_016857690.1
XM_017002202.1 Intron XP_016857691.1
XM_017002203.1 Intron XP_016857692.1
XM_017002204.1 Intron XP_016857693.1

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