Product Details

SNP ID
rs1063455
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.10:103277485 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CACCAACGAGTACAAGATCATCCGC[A/T]CCAACGAGAAGGAGCAGCTGCAGGG
Phenotype
MIM: 605338
Polymorphism
A/T, Transversion Substitution
Allele Nomenclature
Literature Links
INA PubMed Links

Gene Details

Gene
INA
Gene Name
internexin neuronal intermediate filament protein alpha
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_032727.3 323 Missense Mutation ACC,TCC T92S NP_116116.1

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