Product Details

SNP ID

rs1057303

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:807215 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CACGGTGATCCTAAATGTGCATGCG[C/T]GGAGTATGTCCCGTTAGGACAGGGG

Phenotype

MIM: 616513

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

LARP4B PubMed Links

Additional Information

For this assay, SNP(s) [rs79219653] 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

LARP4B

Gene Name

La ribonucleoprotein domain family member 4B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015155.2	8245	UTR 3			NP_055970.1
XM_005252432.3	8245	Intron			XP_005252489.1
XM_005252435.3	8245	Intron			XP_005252492.1
XM_011519435.2	8245	Intron			XP_011517737.1
XM_017015987.1	8245	Intron			XP_016871476.1
XM_017015988.1	8245	Intron			XP_016871477.1
XM_017015989.1	8245	Intron			XP_016871478.1
XM_017015990.1	8245	Intron			XP_016871479.1
XM_017015991.1	8245	Intron			XP_016871480.1
XM_017015992.1	8245	Intron			XP_016871481.1
XM_017015993.1	8245	Intron			XP_016871482.1
XM_017015994.1	8245	Intron			XP_016871483.1
XM_017015995.1	8245	Intron			XP_016871484.1

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