Product Details

SNP ID

rs114667483

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:34657322 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGTGTCGGTTTAGTTTCTGCGGTTT[G/T]CAGGGTTGACATCCTAACTCCTTTG

Phenotype

MIM: 606586

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

LOC105374753 PubMed Links

Additional Information

For this assay, SNP(s) [rs4024086] 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

LOC105374753

Gene Name

uncharacterized LOC105374753

There are no transcripts associated with this gene.

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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