Product Details

SNP ID
rs145379693
Assay Type
Functionally Tested
NCBI dbSNP Submissions
4
Location
Chr.1:161707246 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGAAAATCAGTGTTGGGGTTGCAGG[A/T]GACCTAAACACAGTCACCATGAAGC
Phenotype
MIM: 606891
Polymorphism
A/T, Transversion Substitution
Allele Nomenclature
Literature Links
FCRLA PubMed Links

Gene Details

Gene
FCRLA
Gene Name
Fc receptor like A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001184866.1 275 Silent Mutation GGA,GGT G11G NP_001171795.1
NM_001184867.1 275 Silent Mutation GGA,GGT G11G NP_001171796.1
NM_001184870.1 275 Silent Mutation GGA,GGT G11G NP_001171799.1
NM_001184871.1 275 Silent Mutation GGA,GGT G11G NP_001171800.1
NM_001184872.1 275 Silent Mutation GGA,GGT G11G NP_001171801.1
NM_001184873.1 275 Silent Mutation GGA,GGT G11G NP_001171802.1
NM_032738.3 275 Silent Mutation GGA,GGT G11G NP_116127.3
XM_006711581.3 275 Silent Mutation GGA,GGT G11G XP_006711644.1
XM_011510064.1 275 UTR 5 XP_011508366.1
XM_011510065.1 275 Silent Mutation GGA,GGT G11G XP_011508367.1
XM_011510066.1 275 Silent Mutation GGA,GGT G11G XP_011508368.1

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