Product Details

SNP ID
rs200347901
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:34567915 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GACAACATAATTGTTGGGAAGTTTC[A/G]GCCTGTAGAACATCTTTATTTTTTG
Phenotype
MIM: 606098
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SNX6 PubMed Links

Gene Details

Gene
SNX6
Gene Name
sorting nexin 6
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_021249.3 1169 Silent Mutation GCC,GCT A224A NP_067072.3
NM_152233.2 1169 Silent Mutation GCC,GCT A352A NP_689419.2
XM_006720224.1 1169 Silent Mutation GCC,GCT A315A XP_006720287.1

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