Product Details

SNP ID
rs150726730
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.X:46843744 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATATTTCACAAAATGGTAAGCTAAT[A/G]TAAATGTAGTACTTCAGTTTCTCGA
Phenotype
MIM: 300757
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
RP2 PubMed Links

Gene Details

Gene
RP2
Gene Name
retinitis pigmentosa 2 (X-linked recessive)
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006915.2 Intron NP_008846.2

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