Product Details

SNP ID
rs745959
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.19:32879255 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GAGAGACGCCATTGAGGCTGGGGGC[A/C]ACCAGAGCTCTGGGGTTGTCCTGCA
Phenotype
MIM: 615470 MIM: 604144
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
CEP89 PubMed Links

Gene Details

Gene
CEP89
Gene Name
centrosomal protein 89
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_032816.4 2414 Silent Mutation GTG,GTT V753V NP_116205.3
XM_005259344.3 2414 Silent Mutation GTG,GTT V729V XP_005259401.1
XM_011527425.2 2414 Silent Mutation GTG,GTT V506V XP_011525727.1
XM_017027398.1 2414 Intron XP_016882887.1
Gene
SLC7A9
Gene Name
solute carrier family 7 member 9
There are no transcripts associated with this gene.

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