Product Details

SNP ID
rs150330215
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:33294546 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATTGGTAGAAGAAATTACAGTTCAC[C/T]ACCTCCCTGTCACCTTTCCAGGCAG
Phenotype
MIM: 603255
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
NFX1 PubMed Links

Gene Details

Gene
NFX1
Gene Name
nuclear transcription factor, X-box binding 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001318758.1 308 Missense Mutation CCA,CTA P51L NP_001305687.1
NM_002504.5 308 Missense Mutation CCA,CTA P51L NP_002495.2
NM_147134.3 308 Missense Mutation CCA,CTA P51L NP_667345.1

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