Product Details

SNP ID

rs11920543

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:121781850 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGAGCAAATAGTTTCTTTTTCTTAC[A/G]GCACTTCGCTAGGAATTTAAGCGCC

Phenotype

MIM: 609237

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

IQCB1 PubMed Links

Additional Information

For this assay, SNP(s) [rs17849995] 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

IQCB1

Gene Name

IQ motif containing B1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001023570.3	1202	Intron			NP_001018864.2
NM_001023571.3	1202	Intron			NP_001018865.2
NM_001319107.1	1202	Intron			NP_001306036.1
XM_005247911.3	1202	Intron			XP_005247968.1
XM_005247912.2	1202	Intron			XP_005247969.1
XM_011513335.2	1202	Intron			XP_011511637.1
XM_017007537.1	1202	Intron			XP_016863026.1
XM_017007538.1	1202	Missense Mutation	CGT,TGT	R251C	XP_016863027.1
XM_017007539.1	1202	Intron			XP_016863028.1

View Full Product Details