Product Details

SNP ID

rs7186168

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:87952530 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGATAAGAGGAGGCAGTTGTAGGGT[C/T]CACTTTTAGCTGGAAGTTCTTAGGG

Phenotype

MIM: 611564

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

BANP PubMed Links

Additional Information

For this assay, SNP(s) [rs75570119] 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

BANP

Gene Name

BTG3 associated nuclear protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001173539.1		Intron			NP_001167010.1
NM_001173540.1		Intron			NP_001167011.1
NM_001173541.1		Intron			NP_001167012.1
NM_001173542.1		Intron			NP_001167013.1
NM_001173543.1		Intron			NP_001167014.1
NM_017869.3		Intron			NP_060339.2
NM_079837.2		Intron			NP_524576.2
XM_005256008.3		Intron			XP_005256065.1
XM_005256009.3		Intron			XP_005256066.1
XM_011523170.2		Intron			XP_011521472.1
XM_011523172.2		Intron			XP_011521474.1
XM_011523174.2		Intron			XP_011521476.1
XM_011523175.2		Intron			XP_011521477.1
XM_011523176.2		Intron			XP_011521478.1
XM_011523177.2		Intron			XP_011521479.1
XM_011523178.2		Intron			XP_011521480.1
XM_011523179.2		Intron			XP_011521481.1
XM_011523180.2		Intron			XP_011521482.1
XM_011523181.2		Intron			XP_011521483.1
XM_011523182.1		Intron			XP_011521484.1
XM_011523183.2		Intron			XP_011521485.1
XM_011523184.2		Intron			XP_011521486.1
XM_011523186.2		Intron			XP_011521488.1
XM_017023378.1		Intron			XP_016878867.1
XM_017023379.1		Intron			XP_016878868.1
XM_017023380.1		Intron			XP_016878869.1
XM_017023381.1		Intron			XP_016878870.1
XM_017023382.1		Intron			XP_016878871.1
XM_017023383.1		Intron			XP_016878872.1

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