Product Details

SNP ID

rs903

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:41501085 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGGTCAGAGAGGAGAGAGATCCGAC[A/C]GGAAGAGAAGAGCACAGAGGGCCCA

Phenotype

MIM: 148065

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

KRT13 PubMed Links

Additional Information

For this assay, SNP(s) [rs3169911] 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

KRT13

Gene Name

keratin 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002274.3	1585	UTR 3			NP_002265.2
NM_153490.2	1585	UTR 3			NP_705694.2

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