Product Details

SNP ID

rs59168537

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:44036279 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGTTGCAGTATCTTTTGGCTTTCCA[C/G]GTCTCTAAAATGTTTTTCAACCTGA

Phenotype

MIM: 611793

Polymorphism

C/G, Transversion 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	840	Missense Mutation	CTG,GTG	L173V	NP_689557.1
XM_011524309.2	840	Intron			XP_011522611.1

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