Product Details

SNP ID

rs735534

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:75439343 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGCTGTGCTGCCCTCTGAGTGGGAC[A/G]GACTGTCCTGGGGTCAAAGGAGAGA

Phenotype

MIM: 614537

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

C10orf11 PubMed Links

Additional Information

For this assay, SNP(s) [rs113523996] 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

C10orf11

Gene Name

chromosome 10 open reading frame 11

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001305581.1		Intron			NP_001292510.1
NM_032024.4		Intron			NP_114413.1
XM_011540256.2		Intron			XP_011538558.1
XM_011540257.2		Intron			XP_011538559.1
XM_017016759.1		Intron			XP_016872248.1
XM_017016760.1		Intron			XP_016872249.1
XM_017016761.1		Intron			XP_016872250.1
XM_017016762.1		Intron			XP_016872251.1

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