Product Details

SNP ID

rs17017534

Assay Type

Functionally tested

NCBI dbSNP Submissions

35

Location

Chr.1:211479451 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCAATTAGTCCACTCTACTCTGCTC[C/T]TGAAGCGAATCAGGAACCACCCCAC

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		Intron			NP_001158160.1
NM_183059.2		Intron			NP_898882.1
XM_017001151.1		Intron			XP_016856640.1

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