Product Details

SNP ID
rs77185976
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:35562442 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTTCTGAGGGTATGTTCTGGGAAGT[G/T]GGGGGAGATGTTTGGGGTCCTGGGC
Phenotype
MIM: 611053
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
FAM166B PubMed Links

Gene Details

Gene
FAM166B
Gene Name
family with sequence similarity 166 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001099951.3 748 Silent Mutation NP_001093421.1
NM_001164310.2 748 Missense Mutation NP_001157782.1
NM_001287238.1 748 Missense Mutation NP_001274167.1
NM_001287239.1 748 Missense Mutation NP_001274168.1
XM_011518028.2 748 Missense Mutation XP_011516330.1
Gene
RUSC2
Gene Name
RUN and SH3 domain containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001135999.1 748 Intron NP_001129471.1
XM_006716896.2 748 Intron XP_006716959.1

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