Product Details

SNP ID
rs183247852
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:48112071 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGCTTTTGGTGTAGGATGTCGGAG[A/C]ACCAAGAACAGGAGGTAAGAGTATG
Phenotype
MIM: 614906
Polymorphism
A/C, Transversion 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_013323.2 295 Missense Mutation AAC,CAC N10H NP_037455.2
NM_152244.1 295 Missense Mutation AAC,CAC N10H NP_689450.1
XM_005257260.3 295 Missense Mutation AAC,CAC N10H XP_005257317.1
XM_005257261.3 295 UTR 5 XP_005257318.1
XM_005257262.3 295 UTR 5 XP_005257319.1
XM_011524697.2 295 Missense Mutation AAC,CAC N10H XP_011522999.1

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