Product Details

SNP ID

rs1063457

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:103277998 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GACTGTGGCTAAACCAGACCTGACC[G/T]CGGCTCTGAGGGAGATCCGCGCCCA

Phenotype

MIM: 605338

Polymorphism

G/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	836	Missense Mutation	GCG,TCG	A263S	NP_116116.1

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