Product Details

SNP ID

rs2276321

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:88731287 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACAAGAGGGATGGGTGTGTGTGGTG[C/T]GGCGGGGGGGAAGGGAGGGTGGGGG

Phenotype

MIM: 613299 MIM: 613300

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

FAM13A PubMed Links

Additional Information

For this assay, SNP(s) [rs537100016] 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

FAM13A

Gene Name

family with sequence similarity 13 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001015045.2		Intron			NP_001015045.1
NM_001265578.1		Intron			NP_001252507.1
NM_001265579.1		Intron			NP_001252508.1
NM_001265580.1		Intron			NP_001252509.1
NM_014883.3		Intron			NP_055698.2
XM_005262681.2		Intron			XP_005262738.1
XM_005262682.2		Intron			XP_005262739.1
XM_005262683.2		Intron			XP_005262740.1
XM_005262684.3		Intron			XP_005262741.1
XM_006714057.3		Intron			XP_006714120.1
XM_011531516.1		Intron			XP_011529818.1
XM_011531517.1		Intron			XP_011529819.1
XM_011531518.1		Intron			XP_011529820.1
XM_011531519.2		Intron			XP_011529821.1
XM_017007624.1		Intron			XP_016863113.1
XM_017007625.1		Intron			XP_016863114.1
XM_017007626.1		Intron			XP_016863115.1
XM_017007627.1		Intron			XP_016863116.1
XM_017007628.1		Intron			XP_016863117.1
XM_017007629.1		Intron			XP_016863118.1
XM_017007630.1		Intron			XP_016863119.1
XM_017007631.1		Intron			XP_016863120.1
XM_017007632.1		Intron			XP_016863121.1
XM_017007633.1		Intron			XP_016863122.1
XM_017007634.1		Intron			XP_016863123.1

Gene

FAM13A-AS1

Gene Name

FAM13A antisense RNA 1

There are no transcripts associated with this gene.

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