Product Details

SNP ID
rs113601846
Assay Type
Functionally Tested
NCBI dbSNP Submissions
6
Location
Chr.1:211477151 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CATATAGGTCACAAAAAAGCACAGC[C/T]TGGACCCACATCAAAAGTTTGGCAG
Phenotype
MIM: 180040
Polymorphism
C/T, 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 3004 UTR 3 NP_001158160.1
NM_183059.2 3004 UTR 3 NP_898882.1
XM_017001151.1 3004 UTR 3 XP_016856640.1

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