Product Details

SNP ID

rs2277868

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.20:17699899 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTGCAGCCCTTTTTGTGCTCACCCC[C/T]GACCTGTGGTGTGACATCACAATGT

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

BANF2 PubMed Links

Additional Information

For this assay, SNP(s) [rs117938729] are located under a probe 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

BANF2

Gene Name

barrier to autointegration factor 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001014977.3		Intron			NP_001014977.2
NM_001159495.1		Intron			NP_001152967.1
NM_178477.4		Intron			NP_848572.3
XM_005260668.3		Intron			XP_005260725.1
XM_011529170.1		Intron			XP_011527472.1
XM_011529171.2		Intron			XP_011527473.1

Gene

LOC105372547

Gene Name

uncharacterized LOC105372547

There are no transcripts associated with this gene.

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