Product Details

SNP ID

rs78436786

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:193243236 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTAAAGATTGTAGTAGAGGATGTT[A/G]TAAATGTGTCTTTAATTGGTTCTGT

Phenotype

MIM: 606487

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

HRASLS PubMed Links

Additional Information

For this assay, SNP(s) [rs5855473] 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

HRASLS

Gene Name

HRAS like suppressor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020386.4		Intron			NP_065119.2
XM_011513034.1		Intron			XP_011511336.1
XM_011513035.2		Intron			XP_011511337.1
XM_011513037.2		Intron			XP_011511339.1
XM_017006923.1		Intron			XP_016862412.1

Gene

MGC2889

Gene Name

uncharacterized protein MGC2889

There are no transcripts associated with this gene.

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