Product Details
- SNP ID
-
rs7276859
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.21:44666802 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGCACACAGCAGGATGCCTGGCAGG[A/G]GCTGGGCACACAACAGGCTGGCTGG
- Phenotype
-
MIM: 612920
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
KRTAP12-2
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs7275281] are located under a probe and SNP(s) [rs55914221] 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
- KRTAP12-2
- Gene Name
- keratin associated protein 12-2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_181684.2 |
126 |
Missense Mutation |
CCC,TCC |
P29S |
NP_859012.1 |
- Gene
- KRTAP12-3
- Gene Name
- keratin associated protein 12-3
There are no transcripts associated with this gene.
- Gene
- TSPEAR
- Gene Name
- thrombospondin type laminin G domain and EAR repeats
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