Product Details

SNP ID
rs201442232
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:34567934 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGTTTCGGCCTGTAGAACATCTTTA[C/T]TTTTTGCTCTTGCTTTATCCAGTGC
Phenotype
MIM: 606098
Polymorphism
C/T, 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 1150 Missense Mutation AAT,AGT N218S NP_067072.3
NM_152233.2 1150 Missense Mutation AAT,AGT N346S NP_689419.2
XM_006720224.1 1150 Missense Mutation AAT,AGT N309S XP_006720287.1

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