Product Details

SNP ID

rs148522459

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:63643841 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTCTTGGGTGGGGAGGAGAGCATA[C/G]GGCTCTCTGGGGACAGGTCAGAAGG

Phenotype

MIM: 608362

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

STMN3 PubMed Links

Gene Details

Gene

STMN3

Gene Name

stathmin 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001276310.1	471	Missense Mutation	CCT,CGT	P58R	NP_001263239.1
NM_015894.3	471	Missense Mutation	CCT,CGT	P69R	NP_056978.2

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