Product Details

SNP ID

rs34826388

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:106307756 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGCCTTGTTTGTCTGTTGAAGAAT[A/G]TGGTGTTATCCTGACATAAAACTGT

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

TCP11L2 PubMed Links

Additional Information

For this assay, SNP(s) [rs79057663] 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

TCP11L2

Gene Name

t-complex 11 like 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001286262.1		Intron			NP_001273191.1
NM_152772.2		Intron			NP_689985.1
XM_005268767.4		Intron			XP_005268824.1
XM_005268768.4		Intron			XP_005268825.1
XM_011538129.2		Intron			XP_011536431.1
XM_011538130.2		Intron			XP_011536432.1
XM_011538131.2		Intron			XP_011536433.1
XM_011538132.2		Intron			XP_011536434.1
XM_017019127.1		Intron			XP_016874616.1
XM_017019128.1		Intron			XP_016874617.1
XM_017019129.1		Intron			XP_016874618.1
XM_017019130.1		Intron			XP_016874619.1
XM_017019131.1		Intron			XP_016874620.1
XM_017019132.1		Intron			XP_016874621.1
XM_017019133.1		Intron			XP_016874622.1

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