Product Details

SNP ID

rs116195801

Assay Type

Functionally Tested

NCBI dbSNP Submissions

16

Location

Chr.1:151047925 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCGGGCGGCGGGGGCCCAAGGCCT[A/G]ACCCAGACTCCGACCGAAATGCAGC

Phenotype

MIM: 611275

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

BNIPL PubMed Links

Additional Information

For this assay, SNP(s) [rs115769286] 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

BNIPL

Gene Name

BCL2 interacting protein like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001159642.1	143	Intron			NP_001153114.1
NM_138278.3	143	Intron			NP_612122.2
XM_011509236.1	143	Intron			XP_011507538.1
XM_017000420.1	143	Intron			XP_016855909.1

Gene

C1orf56

Gene Name

chromosome 1 open reading frame 56

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_017860.3	143	Silent Mutation	CTA,CTG	L26L	NP_060330.2

Gene

CDC42SE1

Gene Name

CDC42 small effector 1

There are no transcripts associated with this gene.

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