Product Details

SNP ID
rs8080662
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.17:48113457 on Build GRCh38
Set Membership
HapMap Validated
Context Sequence [VIC/FAM]
TGTGACTGGCTTTTTGGGTGCTTAT[A/G]TAGGAACTGGAGTTGACAATGAAGA
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 Intron NP_037455.2
NM_152244.1 Intron NP_689450.1
XM_005257260.3 Intron XP_005257317.1
XM_005257261.3 Intron XP_005257318.1
XM_005257262.3 Intron XP_005257319.1
XM_011524697.2 Intron XP_011522999.1

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