Product Details

SNP ID

rs35725746

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:40329918 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTCCTCGTATGGATATGTTCTTCG[G/T]GTTCTCTCTCTTTGCTCTTGTTGCT

Phenotype

MIM: 180240

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

LOC105371934 PubMed Links

Additional Information

For this assay, SNP(s) [rs140446425] 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

LOC105371934

Gene Name

uncharacterized LOC105371934

There are no transcripts associated with this gene.

Gene

RARA

Gene Name

retinoic acid receptor alpha

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000964.3		Intron			NP_000955.1
NM_001024809.3		Intron			NP_001019980.1
NM_001145301.2		Intron			NP_001138773.1
NM_001145302.2		Intron			NP_001138774.1
XM_005257552.4		Intron			XP_005257609.1
XM_005257553.1		Intron			XP_005257610.1
XM_005257554.1		Intron			XP_005257611.1
XM_011525095.1		Intron			XP_011523397.1
XM_011525096.1		Intron			XP_011523398.1
XM_017024920.1		Intron			XP_016880409.1

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