Product Details

SNP ID

rs1555897

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:807734 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATGCTCCGAGACATCACACACTTGG[A/C]TATGGCCTGGGCTGACATAAGTTCC

Phenotype

MIM: 616513

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

LARP4B PubMed Links

Additional Information

For this assay, SNP(s) [rs146171221] 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	7726	UTR 3			NP_055970.1
XM_005252432.3	7726	Intron			XP_005252489.1
XM_005252435.3	7726	Intron			XP_005252492.1
XM_011519435.2	7726	Intron			XP_011517737.1
XM_017015987.1	7726	Intron			XP_016871476.1
XM_017015988.1	7726	Intron			XP_016871477.1
XM_017015989.1	7726	Intron			XP_016871478.1
XM_017015990.1	7726	Intron			XP_016871479.1
XM_017015991.1	7726	Intron			XP_016871480.1
XM_017015992.1	7726	Intron			XP_016871481.1
XM_017015993.1	7726	Intron			XP_016871482.1
XM_017015994.1	7726	Intron			XP_016871483.1
XM_017015995.1	7726	Intron			XP_016871484.1

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