Product Details

SNP ID

rs2676080

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.15:33315125 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAAGGCACTTGGGCTGAAAATCAAG[C/G]ATTGGTCCCTTGTCTTGGGTTCCTG

Phenotype

MIM: 180903

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

LOC101928134 PubMed Links

Additional Information

For this assay, SNP(s) [rs77525280] 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

LOC101928134

Gene Name

uncharacterized LOC101928134

There are no transcripts associated with this gene.

Gene

RYR3

Gene Name

ryanodine receptor 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001036.4		Intron			NP_001027.3
NM_001243996.2		Intron			NP_001230925.1
XM_011521880.2		Intron			XP_011520182.1
XM_017022468.1		Intron			XP_016877957.1
XM_017022469.1		Intron			XP_016877958.1
XM_017022470.1		Intron			XP_016877959.1
XM_017022471.1		Intron			XP_016877960.1
XM_017022472.1		Intron			XP_016877961.1
XM_017022473.1		Intron			XP_016877962.1
XM_017022474.1		Intron			XP_016877963.1
XM_017022475.1		Intron			XP_016877964.1
XM_017022476.1		Intron			XP_016877965.1
XM_017022477.1		Intron			XP_016877966.1

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