Product Details

SNP ID

rs199781088

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:49587606 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTTCAGGCTTTTGTGGCAGGAGGAC[G/T]ACACGTCCAGTGTCAACAGCCGGGG

Phenotype

Polymorphism

G/T, 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
XM_006719626.2		Intron			XP_006719689.1
XM_006719627.3		Intron			XP_006719690.1
XM_011538797.2		Intron			XP_011537099.1

Gene

LOC100422296

Gene Name

Parkinsonism associated deglycase pseudogene

There are no transcripts associated with this gene.

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