Product Details

SNP ID

rs1537318

Assay Type

Functionally tested

NCBI dbSNP Submissions

32

Location

Chr.1:197084264 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACACGGAGAGCAAAAATCACTTTAC[A/G]TACTCATGATTGGCTTTAATATTTC

Phenotype

MIM: 605481

Polymorphism

A/G, 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	10751	UTR 3			NP_001193775.1
NM_018136.4	10751	UTR 3			NP_060606.3

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