Product Details

SNP ID
rs150649147
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:18349371 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTTTGCCGTGGTGCTTGAGATAGTA[C/T]CGCTGGTTCTGAAAGAACTTGATGA
Phenotype
MIM: 602075
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SATB1 PubMed Links

Gene Details

Gene
SATB1
Gene Name
SATB homeobox 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001131010.3 2372 Silent Mutation CGA,CGG R697R NP_001124482.1
NM_001195470.2 2372 Silent Mutation CGA,CGG R729R NP_001182399.1
NM_001322871.1 2372 Silent Mutation CGA,CGG R729R NP_001309800.1
NM_001322872.1 2372 Silent Mutation CGA,CGG R697R NP_001309801.1
NM_001322873.1 2372 Silent Mutation CGA,CGG R697R NP_001309802.1
NM_001322874.1 2372 Silent Mutation CGA,CGG R697R NP_001309803.1
NM_001322875.1 2372 Silent Mutation CGA,CGG R697R NP_001309804.1
NM_001322876.1 2372 Silent Mutation CGA,CGG R625R NP_001309805.1
NM_002971.5 2372 Silent Mutation CGA,CGG R697R NP_002962.1
XM_011533988.2 2372 Silent Mutation CGA,CGG R729R XP_011532290.1
XM_011533989.2 2372 Silent Mutation CGA,CGG R729R XP_011532291.1
XM_011533990.2 2372 Intron XP_011532292.1

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