Product Details

SNP ID

rs1351977

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:124807752 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATAAAGTATTCCTTACCCACCAATG[A/G]GGGTGACTTTCACTGAATTGCTGTG

Phenotype

MIM: 611144

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

FAM175B PubMed Links

Additional Information

For this assay, SNP(s) [rs76823488] 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

FAM175B

Gene Name

family with sequence similarity 175 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032182.3		Intron			NP_115558.3
XM_011539554.1		Intron			XP_011537856.1
XM_017015986.1		Intron			XP_016871475.1

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