Product Details

SNP ID
rs6780
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:71059642 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CAGTCAGAATCAGCAATCCTTTTCC[A/C]CAGTGCCCTGCATAGAAAACTCCAA
Phenotype
MIM: 300883
Polymorphism
A/C, Transversion 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 2005 UTR 3 NP_001243114.1
NM_001256186.1 2005 UTR 3 NP_001243115.1
NM_001256187.1 2005 UTR 3 NP_001243116.1
NM_001256188.1 2005 UTR 3 NP_001243117.1
NM_013346.3 2005 UTR 3 NP_037478.2

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