Product Details

SNP ID

rs7219968

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:32167019 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TATGGCAGCTATATATAGGCTTACA[A/C]AATGTAAATAGTAAGCCTAAATAAT

Phenotype

MIM: 613888

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

RHOT1 PubMed Links

Additional Information

For this assay, SNP(s) [rs186570488] 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

RHOT1

Gene Name

ras homolog family member T1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001033566.2		Intron			NP_001028738.1
NM_001033567.2		Intron			NP_001028739.2
NM_001033568.2		Intron			NP_001028740.1
NM_001288754.1		Intron			NP_001275683.1
NM_001288755.1		Intron			NP_001275684.1
NM_001288758.1		Intron			NP_001275687.1
NM_018307.4		Intron			NP_060777.3
XM_011524969.2		Intron			XP_011523271.1
XM_011524971.2		Intron			XP_011523273.2
XM_011524973.2		Intron			XP_011523275.2
XM_011524975.2		Intron			XP_011523277.1
XM_011524976.2		Intron			XP_011523278.2
XM_017024819.1		Intron			XP_016880308.1
XM_017024820.1		Intron			XP_016880309.1
XM_017024821.1		Intron			XP_016880310.1
XM_017024822.1		Intron			XP_016880311.1
XM_017024823.1		Intron			XP_016880312.1
XM_017024824.1		Intron			XP_016880313.1
XM_017024825.1		Intron			XP_016880314.1

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