Product Details

SNP ID

rs16909145

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.9:93453905 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGACAGGATGAGCTGCACTGACTTG[C/G]CTTTGGTAACCGCACAGCTCTCTAC

Phenotype

MIM: 612265

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

FAM120A PubMed Links

Additional Information

For this assay, SNP(s) [rs79469056] 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

FAM120A

Gene Name

family with sequence similarity 120A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001286722.1		Intron			NP_001273651.1
NM_001286723.1		Intron			NP_001273652.1
NM_001286724.1		Intron			NP_001273653.1
NM_014612.4		Intron			NP_055427.2
XM_005251842.4		Intron			XP_005251899.1
XM_011518412.2		Intron			XP_011516714.1
XM_011518413.2		Intron			XP_011516715.1
XM_011518414.2		Intron			XP_011516716.1
XM_011518416.2		Intron			XP_011516718.1

Gene

FAM120AOS

Gene Name

family with sequence similarity 120A opposite strand

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001322224.1		Intron			NP_001309153.1
NM_198841.2		Intron			NP_942138.2

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