Product Details

SNP ID

rs6859682

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:34668692 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTTTATGAGCTTTTTTAAATTGGG[A/G]AAAAAAAACTATTTAAAATATCGGC

Phenotype

MIM: 606586

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

RAI14 PubMed Links

Additional Information

For this assay, SNP(s) [rs34204364] 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

RAI14

Gene Name

retinoic acid induced 14

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145520.1		Intron			NP_001138992.1
NM_001145521.1		Intron			NP_001138993.1
NM_001145522.1		Intron			NP_001138994.1
NM_001145523.1		Intron			NP_001138995.1
NM_001145525.1		Intron			NP_001138997.1
NM_015577.2		Intron			NP_056392.2
XM_006714469.2		Intron			XP_006714532.1
XM_011514016.2		Intron			XP_011512318.2
XM_011514017.2		Intron			XP_011512319.1
XM_011514018.1		Intron			XP_011512320.1
XM_011514019.1		Intron			XP_011512321.1
XM_011514020.1		Intron			XP_011512322.1
XM_011514021.1		Intron			XP_011512323.1
XM_011514022.1		Intron			XP_011512324.1
XM_011514023.1		Intron			XP_011512325.1
XM_011514024.1		Intron			XP_011512326.1
XM_011514025.2		Intron			XP_011512327.2
XM_017009334.1		Intron			XP_016864823.1
XM_017009335.1		Intron			XP_016864824.1
XM_017009336.1		Intron			XP_016864825.1

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