Product Details

SNP ID

rs150108952

Assay Type

Functionally tested

NCBI dbSNP Submissions

6

Location

Chr.1:197084342 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACATTTACTAATAAGGAATGCCAAG[C/T]GTATCCATCACCATTTGAATAGCTT

Phenotype

MIM: 605481

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

ASPM PubMed Links

Gene Details

Gene

ASPM

Gene Name

abnormal spindle microtubule assembly

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001206846.1	10673	Silent Mutation	ACA,ACG	T1887T	NP_001193775.1
NM_018136.4	10673	Silent Mutation	ACA,ACG	T3472T	NP_060606.3

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