Product Details

SNP ID
rs35258126
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:52459396 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATAGGTTGCCGGTGACAGAATGCGT[C/T]GTCAGACTTTAAGAAGGGCACTTAG
Phenotype
MIM: 615507 MIM: 191040
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
NISCH PubMed Links
Additional Information
For this assay, SNP(s) [rs112833562] 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
NISCH
Gene Name
nischarin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001276293.1 Intron NP_001263222.1
NM_001276294.1 Intron NP_001263223.1
NM_007184.3 Intron NP_009115.2
XM_005264839.2 Intron XP_005264896.1
XM_006712955.2 Intron XP_006713018.1
XM_017005643.1 Intron XP_016861132.1
Gene
TNNC1
Gene Name
troponin C1, slow skeletal and cardiac type
There are no transcripts associated with this gene.

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