Product Details

SNP ID

rs2697655

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:10760011 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCAGGACTTGGGTACAGGGATCTGT[A/G]ATAACATTAACTGAGGAAAATAGGG

Phenotype

MIM: 600280

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

NUBP1 PubMed Links

Additional Information

For this assay, SNP(s) [rs115914510] are located under a probe and SNP(s) [rs74988634] 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

NUBP1

Gene Name

nucleotide binding protein 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001278506.1		Intron			NP_001265435.1
NM_001323594.1		Intron			NP_001310523.1
NM_001323595.1		Intron			NP_001310524.1
NM_001323596.1		Intron			NP_001310525.1
NM_001323597.1		Intron			NP_001310526.1
NM_002484.3		Intron			NP_002475.2
XM_017023252.1		Intron			XP_016878741.1

Gene

TVP23A

Gene Name

trans-golgi network vesicle protein 23 homolog A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001079512.3		Intron			NP_001072980.1
NM_001318873.1		Intron			NP_001305802.1
XM_006720944.3		Intron			XP_006721007.1
XM_011522654.2		Intron			XP_011520956.1
XM_017023649.1		Intron			XP_016879138.1
XM_017023650.1		Intron			XP_016879139.1
XM_017023651.1		Intron			XP_016879140.1

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