Product Details

SNP ID
rs191229840
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:48113309 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTGCTTTCATGTATAGACCAACAG[C/T]AAAGCCTTTACTGCCAAGACTTCCT
Phenotype
MIM: 614906
Polymorphism
C/T, 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_013323.2 405 Silent Mutation AGC,AGT S46S NP_037455.2
NM_152244.1 405 Silent Mutation AGC,AGT S46S NP_689450.1
XM_005257260.3 405 Missense Mutation AGC,AGT S46S XP_005257317.1
XM_005257261.3 405 Missense Mutation AGC,AGT S38S XP_005257318.1
XM_005257262.3 405 Missense Mutation AGC,AGT S38S XP_005257319.1
XM_011524697.2 405 Silent Mutation AGC,AGT S46S XP_011522999.1

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