Product Details

SNP ID
rs140234522
Assay Type
Functionally tested
NCBI dbSNP Submissions
16
Location
Chr.1:157515682 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGGAGAGACGTGTGGACTCATCTG[C/T]GAGGAGCTGAGGAAGCCAAGAACAG
Phenotype
MIM: 605877
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FCRL5 PubMed Links

Gene Details

Gene
FCRL5
Gene Name
Fc receptor like 5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001195388.1 3075 Missense Mutation ACA,GCA T973A NP_001182317.1
NM_031281.2 3075 Missense Mutation CAC,CGC H976R NP_112571.2
XM_011510030.1 3075 Missense Mutation CAC,CGC H891R XP_011508332.1
XM_011510031.1 3075 Missense Mutation CAC,CGC H883R XP_011508333.1
XM_011510032.1 3075 Missense Mutation CAC,CGC H883R XP_011508334.1
XM_011510033.1 3075 Intron XP_011508335.1

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