Product Details

SNP ID

rs200007996

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:44040180 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATGGTCTGGAAGAGCTGCTGGCCC[C/T]CTAGAGAGACACCAGCACTGATTGC

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	658	Missense Mutation	GAG,GGG	E112G	NP_689557.1
XM_011524309.2	658	Intron			XP_011522611.1

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