Product Details

SNP ID

rs78910164

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.13:77703286 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATGAATGAGATATTCATCTTCCAC[A/G]TGTAATACCAAGACCCCAGACAGCT

Phenotype

MIM: 610491

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

MIR3665 PubMed Links

Additional Information

For this assay, SNP(s) [rs77310582] 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

MIR3665

Gene Name

microRNA 3665

There are no transcripts associated with this gene.

Gene

SLAIN1

Gene Name

SLAIN motif family member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001040153.3		Intron			NP_001035243.2
NM_001242868.1		Intron			NP_001229797.1
NM_001242869.1		Intron			NP_001229798.1
NM_001242870.1		Intron			NP_001229799.1
NM_001242871.1		Intron			NP_001229800.1
NM_144595.3		Intron			NP_653196.1
XM_011534929.2		Intron			XP_011533231.1
XM_011534930.1		Intron			XP_011533232.1

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