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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