Product Details

SNP ID

rs139855814

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:63642166 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGTGCCTCGCGGATCTCCTTGCTG[A/C]GCTCCATCTTGTAGTTGAGCTTCTC

Phenotype

MIM: 608362

Polymorphism

A/C, 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	690	Missense Mutation	CGC,CTC	R131L	NP_001263239.1
NM_015894.3	690	Missense Mutation	CGC,CTC	R142L	NP_056978.2

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