Product Details

SNP ID

rs17123808

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:49585630 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCAGTGGGCTCAGAGATGAACAGGC[C/T]GTCAGTGCTAGGCAGACCAGGAGAA

Phenotype

Polymorphism

C/T, Transition 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		Intron			NP_115506.1
XM_006719625.2		Intron			XP_006719688.1
XM_006719626.2		Intron			XP_006719689.1
XM_006719627.3		Intron			XP_006719690.1
XM_011538796.2		Intron			XP_011537098.1
XM_011538797.2		Intron			XP_011537099.1
XM_017020008.1		Intron			XP_016875497.1

Gene

LOC100422296

Gene Name

Parkinsonism associated deglycase pseudogene

There are no transcripts associated with this gene.

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