Product Details
- SNP ID
-
rs151047920
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:49070110 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TTCCCTGGGGGTGCCCAGAGTGGAG[A/G]TGGTAGCTCAGGTACCTCCCCGTCC
- Phenotype
-
MIM: 176268
MIM: 162662
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
KCNA7
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs10535426] 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
- KCNA7
- Gene Name
- potassium voltage-gated channel subfamily A member 7
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_031886.2 |
1680 |
Missense Mutation |
CCT,TCT |
P442S |
NP_114092.2 |
- Gene
- NTF4
- Gene Name
- neurotrophin 4
There are no transcripts associated with this gene.
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