Product Details

SNP ID
rs148689952
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:71061941 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGAAAGGGAGCTGCCGCTTCAAGGC[C/T]TTCCCAGGCAGTGGTGGTACTACAA
Phenotype
MIM: 300883
Polymorphism
C/T, 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_001256185.1 430 Silent Mutation AAA,AAG K96K NP_001243114.1
NM_001256186.1 430 Intron NP_001243115.1
NM_001256187.1 430 Intron NP_001243116.1
NM_001256188.1 430 Silent Mutation AAA,AAG K92K NP_001243117.1
NM_013346.3 430 Silent Mutation AAA,AAG K96K NP_037478.2

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