Product Details

SNP ID
rs577597
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:65844295 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATTATCATAAGGACAAACATAGACC[A/C]ATGGAACAGAGAGTCCAAAGTTTAT
Phenotype
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
SNX32 PubMed Links

Gene Details

Gene
SNX32
Gene Name
sorting nexin 32
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_152760.2 Intron NP_689973.2
XM_006718488.3 Intron XP_006718551.1
XM_017017470.1 Intron XP_016872959.1
XM_017017471.1 Intron XP_016872960.1
XM_017017472.1 Intron XP_016872961.1
XM_017017473.1 Intron XP_016872962.1

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