Product Details

SNP ID

rs111856613

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.20:45824640 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACATGTCAAAGGCAGCCTTGAACTC[A/T]GCGAGGGAGGGCAGAGGGCAGAGGT

Phenotype

MIM: 191039 MIM: 605574

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

SNX21 PubMed Links

Additional Information

For this assay, SNP(s) [rs556074291] 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

SNX21

Gene Name

sorting nexin family member 21

There are no transcripts associated with this gene.

Gene

TNNC2

Gene Name

troponin C2, fast skeletal type

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003279.2		Intron			NP_003270.1
XM_011529031.2		Intron			XP_011527333.1

Gene

UBE2C

Gene Name

ubiquitin conjugating enzyme E2 C

There are no transcripts associated with this gene.

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