Product Details

SNP ID

rs1864367

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:53077688 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAATTGCTTCTTGGGAAGCAATTAC[C/T]TGTGACAGGTGCACACTCCCAGCGG

Phenotype

MIM: 611908

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

RFT1 PubMed Links

Additional Information

For this assay, SNP(s) [rs151225962] 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

RFT1

Gene Name

RFT1 homolog

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_052859.3	1418	Intron			NP_443091.1
XM_005265537.4	1418	Intron			XP_005265594.1
XM_006713384.3	1418	Intron			XP_006713447.1
XM_011534214.2	1418	Missense Mutation	AAC,AGC	N450S	XP_011532516.1
XM_011534215.2	1418	Missense Mutation	AAG,AGG	K450R	XP_011532517.1
XM_011534216.2	1418	Intron			XP_011532518.1
XM_017007460.1	1418	UTR 3			XP_016862949.1
XM_017007461.1	1418	Intron			XP_016862950.1

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