Product Details

SNP ID

rs146845592

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:150791570 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGTGGAGGTCTGCTCCCTAGAGGG[C/T]GAAGGGGGCACTGAATTCTCCCCCA

Phenotype

MIM: 610334 MIM: 610385

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

LOC105375566 PubMed Links

Additional Information

For this assay, SNP(s) [rs2302479] 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

LOC105375566

Gene Name

uncharacterized LOC105375566

There are no transcripts associated with this gene.

Gene

TMEM176A

Gene Name

transmembrane protein 176A

There are no transcripts associated with this gene.

Gene

TMEM176B

Gene Name

transmembrane protein 176B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001101311.1	791	Silent Mutation	TCA,TCG	S258S	NP_001094781.1
NM_001101312.1	791	Silent Mutation	TCA,TCG	S258S	NP_001094782.1
NM_001101314.1	791	Silent Mutation	TCA,TCG	S221S	NP_001094784.1
NM_014020.3	791	Silent Mutation	TCA,TCG	S258S	NP_054739.3
XM_006715933.3	791	Silent Mutation	TCA,TCG	S221S	XP_006715996.2

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