Product Details

SNP ID

rs2182661

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:124014451 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CACAAAAAAGCTTGAGTTGGGATCC[G/T]TGCTCCCCTCTCTCTTTGAAGTTTC

Phenotype

MIM: 603759

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

LHX2 PubMed Links

Gene Details

Gene

LHX2

Gene Name

LIM homeobox 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004789.3		Intron			NP_004780.3
XM_006717323.2		Intron			XP_006717386.1

Gene

LOC100505588

Gene Name

uncharacterized LOC100505588

There are no transcripts associated with this gene.

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