Product Details

SNP ID

rs6996977

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:79620748 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTGAAAAATTTAAATATTTAATGA[C/G]TCCATCAACCAATCTGGCCAGAGAA

Phenotype

MIM: 600621

Polymorphism

C/G, Transversion 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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