Product Details

SNP ID
rs11996807
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:79614276 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ATTTCAAAGATAATTAATTATCAGG[A/G]CGAGTGCTTTTTTCCTGATTCATTA
Phenotype
MIM: 600621
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
STMN2 PubMed Links

Gene Details

Gene
STMN2
Gene Name
stathmin 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001199214.1 Intron NP_001186143.1
NM_007029.3 Intron NP_008960.2
XM_005251142.2 Intron XP_005251199.1

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