Product Details
- SNP ID
-
rs1470826
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:208122115 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- TCCTCATTACCGAGCACAGAGATTC[A/G]GTACCTTTTCAAGATTATGAAGTGT
- Phenotype
-
MIM: 123680
MIM: 123690
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
CRYGC
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs78081166] 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
- CRYGC
- Gene Name
- crystallin gamma C
There are no transcripts associated with this gene.
- Gene
- CRYGD
- Gene Name
- crystallin gamma D
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_006891.3 |
|
Intron |
|
|
NP_008822.2 |
- Gene
- LOC100507443
- Gene Name
- uncharacterized LOC100507443
There are no transcripts associated with this gene.
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