Product Details

SNP ID

rs929867

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.16:31180161 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

GCTGCTCAGTCCTCCAGGCGTCGGT[G/A]CTCAGCGGTGTTGGAACTTCGTTGC

Phenotype

MIM: 137070

Polymorphism

G/A, Transition Substitution

Allele Nomenclature

Literature Links

FUS PubMed Links

Additional Information

For this assay, SNP(s) [rs67676356] 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

FUS

Gene Name

FUS RNA binding protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001170634.1	718	UTR 5			NP_001164105.1
NM_001170937.1	718	UTR 5			NP_001164408.1
NM_004960.3	718	UTR 5			NP_004951.1
XM_005255233.4	718	UTR 5			XP_005255290.1
XM_011545781.1	718	UTR 5			XP_011544083.1
XM_011545782.2	718	Intron			XP_011544084.1

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