Product Details

SNP ID

rs756924

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:2301799 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CGTCTCCTCCACATCCCACACCAGG[C/T]CCTGCCCATGACTTTCCCCCTCTCA

Phenotype

MIM: 611033 MIM: 603853

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

C11orf21 PubMed Links

Additional Information

For this assay, SNP(s) [rs114342362] 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

C11orf21

Gene Name

chromosome 11 open reading frame 21

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_011520034.1	115	Silent Mutation	GGA,GGG	G21G	XP_011518336.1

Gene

TSPAN32

Gene Name

tetraspanin 32

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_139022.2	115	Intron			NP_620591.3
XM_005252719.4	115	Intron			XP_005252776.1
XM_005252720.4	115	Intron			XP_005252777.1
XM_011519815.2	115	Intron			XP_011518117.2
XM_011519818.2	115	Intron			XP_011518120.2
XM_011519819.1	115	Intron			XP_011518121.1
XM_011519822.1	115	Intron			XP_011518124.1
XM_011519828.2	115	Intron			XP_011518130.1
XM_011519829.2	115	Intron			XP_011518131.2
XM_017017064.1	115	Intron			XP_016872553.1
XM_017017065.1	115	Intron			XP_016872554.1
XM_017017066.1	115	Intron			XP_016872555.1
XM_017017067.1	115	Intron			XP_016872556.1
XM_017017068.1	115	Intron			XP_016872557.1
XM_017017069.1	115	Intron			XP_016872558.1
XM_017017070.1	115	Intron			XP_016872559.1
XM_017017071.1	115	Intron			XP_016872560.1

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