Product Details

SNP ID
rs76119682
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:49587656 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAATATCTGGGTGTCCCCTCAGCTG[C/G]TCCCGGGGAAGGCTGGCAGGGGTCT
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 2793 Silent Mutation GAC,GAG D877E NP_115506.1
XM_006719625.2 2793 Silent Mutation GAC,GAG D877E XP_006719688.1
XM_006719626.2 2793 Intron XP_006719689.1
XM_006719627.3 2793 Intron XP_006719690.1
XM_011538796.2 2793 Missense Mutation GAC,GAG D877E XP_011537098.1
XM_011538797.2 2793 Intron XP_011537099.1
XM_017020008.1 2793 Silent Mutation GAC,GAG D787E XP_016875497.1
Gene
LOC100422296
Gene Name
Parkinsonism associated deglycase pseudogene
There are no transcripts associated with this gene.

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