Product Details

SNP ID

rs8066666

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:44037818 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGAGCCATAAAAATGTGATAGTGGC[C/T]TCAAGAATCCAAATTAAGATAGCAG

Phenotype

MIM: 611793

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

LSM12 PubMed Links

Gene Details

Gene

LSM12

Gene Name

LSM12 homolog

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152344.3		Intron			NP_689557.1
XM_011524309.2		Intron			XP_011522611.1

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