Product Details

SNP ID
rs117702478
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.7:151430104 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTTGTTGCTGGTTTTGTGGTGGCCT[C/T]TTCCGGTCCTTGATCTGATTGAAGA
Phenotype
MIM: 609603
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
CRYGN PubMed Links
Additional Information
For this assay, SNP(s) [rs73476444] 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
CRYGN
Gene Name
crystallin gamma N
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001308292.1 1769 UTR 3 NP_001295221.1
NM_144727.2 1769 Missense Mutation AAG,GAG K165E NP_653328.1
XM_005249952.3 1769 UTR 3 XP_005250009.1
XM_011515836.1 1769 UTR 3 XP_011514138.1
XM_011515837.2 1769 UTR 3 XP_011514139.1
XM_017011773.1 1769 Intron XP_016867262.1
Gene
MIR3907
Gene Name
microRNA 3907
There are no transcripts associated with this gene.

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