Product Details

SNP ID

rs7987725

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:27549310 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATTCTATATAGAATGTCAACATTTA[C/T]TTTTTAAGAACTGGTTCTTCCTTCG

Phenotype

MIM: 609733

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

LNX2 PubMed Links

Gene Details

Gene

LNX2

Gene Name

ligand of numb-protein X 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_153371.3		Intron			NP_699202.1
XM_011534995.2		Intron			XP_011533297.1
XM_017020434.1		Intron			XP_016875923.1

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