Product Details

SNP ID
rs12304535
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:49583089 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGAGCAAGTTCAGCCACCAGGCCC[C/G]TTAAGCACAGTGCCAAGAGCCTGTG
Phenotype
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
FAM186B PubMed Links

Gene Details

Gene
FAM186B
Gene Name
family with sequence similarity 186 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_032130.2 3159 Intron NP_115506.1
XM_006719625.2 3159 UTR 3 XP_006719688.1
XM_006719626.2 3159 Missense Mutation ACG,AGG T852R XP_006719689.1
XM_006719627.3 3159 Intron XP_006719690.1
XM_011538796.2 3159 Intron XP_011537098.1
XM_011538797.2 3159 Missense Mutation AAC,AAG N795K XP_011537099.1
XM_017020008.1 3159 UTR 3 XP_016875497.1

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