Product Details

SNP ID

rs150662833

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:150801672 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGCTCACCTGCTGCTCTGCGCTGC[A/G]GCCCCGGGCCACCCAGGCCAGGGGC

Phenotype

MIM: 610334 MIM: 610385

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

TMEM176A PubMed Links

Additional Information

For this assay, SNP(s) [rs1127958] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

TMEM176A

Gene Name

transmembrane protein 176A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018487.2	335	Missense Mutation	CAG,CGG	Q41R	NP_060957.2
XM_011516376.2	335	Missense Mutation	CAG,CGG	Q58R	XP_011514678.1
XM_011516377.2	335	Missense Mutation	CAG,CGG	Q58R	XP_011514679.1
XM_011516378.2	335	Missense Mutation	CAG,CGG	Q58R	XP_011514680.1
XM_017012393.1	335	Missense Mutation	CAG,CGG	Q41R	XP_016867882.1

Gene

TMEM176B

Gene Name

transmembrane protein 176B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001101311.1	335	Intron			NP_001094781.1
NM_001101312.1	335	Intron			NP_001094782.1
NM_001101314.1	335	Intron			NP_001094784.1
NM_014020.3	335	Intron			NP_054739.3
XM_006715933.3	335	Intron			XP_006715996.2

View Full Product Details