Product Details

SNP ID
rs111658862
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:48118732 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTTCCTGAACTTCCTGGGAAGTCA[A/G]CCTTCTTCGGCACCTCAGATGAGTT
Phenotype
MIM: 614906
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SNX11 PubMed Links

Gene Details

Gene
SNX11
Gene Name
sorting nexin 11
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_013323.2 526 Missense Mutation ACC,GCC T87A NP_037455.2
NM_152244.1 526 Missense Mutation ACC,GCC T87A NP_689450.1
XM_005257260.3 526 Missense Mutation ACC,GCC T87A XP_005257317.1
XM_005257261.3 526 Missense Mutation ACC,GCC T79A XP_005257318.1
XM_005257262.3 526 Missense Mutation ACC,GCC T79A XP_005257319.1
XM_011524697.2 526 Missense Mutation ACC,GCC T87A XP_011522999.1

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