Product Details

SNP ID
rs10917740
Assay Type
Functionally Tested
NCBI dbSNP Submissions
29
Location
Chr.1:161710222 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GACTCAGACACACCTGCCTTTCCCG[A/C]TCCATTGCTTAGTCTCTTTTTAAGC
Phenotype
MIM: 606891
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
FCRLA PubMed Links
Additional Information
For this assay, SNP(s) [rs113851831] are located under a probe 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
FCRLA
Gene Name
Fc receptor like A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001184866.1 Intron NP_001171795.1
NM_001184867.1 Intron NP_001171796.1
NM_001184870.1 Intron NP_001171799.1
NM_001184871.1 Intron NP_001171800.1
NM_001184872.1 Intron NP_001171801.1
NM_001184873.1 Intron NP_001171802.1
NM_032738.3 Intron NP_116127.3
XM_006711581.3 Intron XP_006711644.1
XM_011510064.1 Intron XP_011508366.1
XM_011510065.1 Intron XP_011508367.1
XM_011510066.1 Intron XP_011508368.1

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