Product Details

SNP ID

rs145475171

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:54519173 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGACGAGATGGTGGGCGCCAACTT[C/T]TTCCTGACCCTTAGCACGCCCCCCG

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SNX18 PubMed Links

Additional Information

For this assay, SNP(s) [rs2548613] 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

SNX18

Gene Name

sorting nexin 18

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001102575.1	1411	Silent Mutation	TTC,TTT	F407F	NP_001096045.1
NM_001145427.1	1411	Silent Mutation	TTC,TTT	F407F	NP_001138899.1
NM_052870.2	1411	Silent Mutation	TTC,TTT	F407F	NP_443102.2
XM_017008997.1	1411	Silent Mutation	TTC,TTT	F407F	XP_016864486.1

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