Product Details

SNP ID

rs248999

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:80498283 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAAATAGGGCCACGTGTTTTCAGTG[A/G]GAGACTGCTTTGGGGATAGTGGATC

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

FAM151B PubMed Links

Additional Information

For this assay, SNP(s) [rs185259796] 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

FAM151B

Gene Name

family with sequence similarity 151 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_205548.2		Intron			NP_991111.2
XM_006714564.3		Intron			XP_006714627.2
XM_011543234.2		Intron			XP_011541536.1
XM_011543235.2		Intron			XP_011541537.1
XM_011543236.2		Intron			XP_011541538.1
XM_011543237.2		Intron			XP_011541539.1
XM_017009166.1		Intron			XP_016864655.1
XM_017009167.1		Intron			XP_016864656.1
XM_017009168.1		Intron			XP_016864657.1
XM_017009169.1		Intron			XP_016864658.1
XM_017009170.1		Intron			XP_016864659.1

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