Product Details

SNP ID
rs111332475
Assay Type
Functionally tested
NCBI dbSNP Submissions
1
Location
Chr.1:157746875 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATTCCAAGGTGTCTAGCTCACCTTG[C/T]TCTCCAGAAGTGTCCTGATGTTTGC
Phenotype
MIM: 606509
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FCRL2 PubMed Links

Gene Details

Gene
FCRL2
Gene Name
Fc receptor like 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001159488.1 1814 Intron NP_001152960.1
NM_030764.3 1814 Missense Mutation AAC,AGC N495S NP_110391.2
XM_006711535.3 1814 Intron XP_006711598.1
XM_011509974.2 1814 Missense Mutation AAC,AGC N495S XP_011508276.1
XM_011509975.2 1814 Missense Mutation AAC,AGC N473S XP_011508277.1
XM_011509976.2 1814 Missense Mutation AAC,AGC N473S XP_011508278.1
XM_017002316.1 1814 Intron XP_016857805.1
XM_017002317.1 1814 Intron XP_016857806.1
XM_017002318.1 1814 Intron XP_016857807.1
XM_017002319.1 1814 Intron XP_016857808.1

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