Product Details

SNP ID

rs7254755

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:17605773 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATAGGGACGAGGTTTCCCCCATCCC[A/G]GCTCAAAATGCCCCCTAGGTGCTGG

Phenotype

MIM: 609894

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

UNC13A PubMed Links

Additional Information

For this assay, SNP(s) [rs201314772] 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

UNC13A

Gene Name

unc-13 homolog A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001080421.2	5535	UTR 3			NP_001073890.2
XM_011527810.2	5535	UTR 3			XP_011526112.1
XM_011527811.2	5535	UTR 3			XP_011526113.1
XM_017026502.1	5535	UTR 3			XP_016881991.1

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