Product Details

SNP ID
rs148189077
Assay Type
Functionally tested
NCBI dbSNP Submissions
3
Location
Chr.1:211479156 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGCTGGCGAAGGGCGAGATGCGCGC[A/G]CGGGTCTTGAAGGTGGCCAGGCTGC
Phenotype
MIM: 180040
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
RD3 PubMed Links

Gene Details

Gene
RD3
Gene Name
retinal degeneration 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001164688.1 999 Silent Mutation CGC,CGT R156R NP_001158160.1
NM_183059.2 999 Silent Mutation CGC,CGT R156R NP_898882.1
XM_017001151.1 999 Silent Mutation CGC,CGT R168R XP_016856640.1

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