Product Details

SNP ID

rs5029929

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:137869500 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTGCCCAATTCCACCTGTAGAGGA[C/T]GTCTGACATCAAAAGAGAGCACCAT

Phenotype

MIM: 191163

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

LOC100130476 PubMed Links

Additional Information

For this assay, SNP(s) [rs5029930] 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

LOC100130476

Gene Name

uncharacterized LOC100130476

There are no transcripts associated with this gene.

Gene

LOC107986649

Gene Name

uncharacterized LOC107986649

There are no transcripts associated with this gene.

Gene

TNFAIP3

Gene Name

TNF alpha induced protein 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001270507.1		Intron			NP_001257436.1
NM_001270508.1		Intron			NP_001257437.1
NM_006290.3		Intron			NP_006281.1
XM_005267119.1		Intron			XP_005267176.1
XM_006715555.1		Intron			XP_006715618.1
XM_011536095.1		Intron			XP_011534397.1
XM_011536096.1		Intron			XP_011534398.1

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