Product Details

SNP ID
rs148619854
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:4778124 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTCTCAGGAGAGGAAATTCACAGTG[C/T]GCCATGTTCTCCACTGCAAGACATG
Phenotype
MIM: 611562
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SEPT12 PubMed Links

Gene Details

Gene
SEPT12
Gene Name
septin 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001154458.2 1101 Silent Mutation GCA,GCG A233A NP_001147930.1
NM_144605.4 1101 Silent Mutation GCA,GCG A279A NP_653206.2
XM_006720846.2 1101 Silent Mutation GCA,GCG A279A XP_006720909.1
XM_011522379.2 1101 Silent Mutation GCA,GCG A215A XP_011520681.1
XM_017022938.1 1101 Silent Mutation GCA,GCG A285A XP_016878427.1

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