Product Details

SNP ID
rs12562148
Assay Type
Functionally tested
NCBI dbSNP Submissions
6
Location
Chr.1:151612132 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGCGTCGGGGGTCGTCCGGCTGCCA[C/G]GCAGGGCGAGCACGCGCCGGGAGGC
Phenotype
MIM: 611541
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
SNX27 PubMed Links

Gene Details

Gene
SNX27
Gene Name
sorting nexin family member 27
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_030918.5 69 Intron NP_112180.4
XM_005245509.2 69 UTR 5 XP_005245566.1
XM_005245510.3 69 Intron XP_005245567.1
XM_005245511.4 69 UTR 5 XP_005245568.1
XM_011510024.2 69 UTR 5 XP_011508326.1
XM_011510025.2 69 UTR 5 XP_011508327.1
XM_011510026.2 69 UTR 5 XP_011508328.1
XM_017002417.1 69 UTR 5 XP_016857906.1

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