Product Details

SNP ID

rs58551885

Assay Type

Functionally tested

NCBI dbSNP Submissions

12

Location

Chr.1:211477997 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGGAAGGACAATGAAGCTGCAGGA[A/T]GCTCTTCTAGAACATTTCACTCAGC

Phenotype

MIM: 180040

Polymorphism

A/T, Transversion 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	2158	UTR 3			NP_001158160.1
NM_183059.2	2158	UTR 3			NP_898882.1
XM_017001151.1	2158	UTR 3			XP_016856640.1

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