Product Details

SNP ID
rs190322760
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:50333936 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGGTTGAATACGTGTATCATTTTC[C/T]TCAGGCACTGATTCCGTTTCTGCCC
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FAM186A PubMed Links

Gene Details

Gene
FAM186A
Gene Name
family with sequence similarity 186 member A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001145475.1 6820 Missense Mutation AAG,AGG K2224R NP_001138947.1
XM_006719231.3 6820 Missense Mutation AAG,AGG K2224R XP_006719294.1
XM_011537890.2 6820 Missense Mutation AAG,AGG K2224R XP_011536192.1
XM_011537892.1 6820 Missense Mutation AAG,AGG K2081R XP_011536194.1

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