Product Details

SNP ID
rs5981065
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:71072350 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GCCAGAAGACAATAATGATCTGAAG[A/G]CAACGAATAAAAATGTTTCTCAAAG
Phenotype
MIM: 300883
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SNX12 PubMed Links

Gene Details

Gene
SNX12
Gene Name
sorting nexin 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001256185.1 Intron NP_001243114.1
NM_001256186.1 Intron NP_001243115.1
NM_001256187.1 Intron NP_001243116.1
NM_001256188.1 Intron NP_001243117.1
NM_013346.3 Intron NP_037478.2

View Full Product Details