Product Details

SNP ID

rs17171304

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:38181070 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGACATTGCTTCTTCTTGGGCTACA[A/G]TAATCATTTGCCTTATTTTCCTTCC

Phenotype

MIM: 611759

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

STARD3NL PubMed Links

Additional Information

For this assay, SNP(s) [rs12535249,rs9639788] 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

STARD3NL

Gene Name

STARD3 N-terminal like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032016.3		Intron			NP_114405.1
XM_005249880.1		Intron			XP_005249937.1
XM_005249881.2		Intron			XP_005249938.1
XM_011515572.1		Intron			XP_011513874.1
XM_017012692.1		Intron			XP_016868181.1
XM_017012693.1		Intron			XP_016868182.1
XM_017012694.1		Intron			XP_016868183.1
XM_017012695.1		Intron			XP_016868184.1
XM_017012696.1		Intron			XP_016868185.1
XM_017012697.1		Intron			XP_016868186.1
XM_017012698.1		Intron			XP_016868187.1

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