Product Details
- SNP ID
-
rs1763613
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
57
- Location
-
Chr.1:16005414 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- CAAAGTTGGGAGGCACTGACATGTT[G/T]GACTCTGTGTTCCTGGAAGGCAGAT
- Phenotype
-
MIM: 610692
- Polymorphism
- G/T, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
C1orf64
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs75084676] 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
- C1orf64
- Gene Name
- chromosome 1 open reading frame 64
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_178840.3 |
|
Intron |
|
|
NP_849162.1 |
- Gene
- HSPB7
- Gene Name
- heat shock protein family B (small) member 7
There are no transcripts associated with this gene.
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