Product Details

SNP ID

rs149961183

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:124019593 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTGTAGTATTTGAATTTCAGGTAA[A/G]CAACAAATACATTTTTAGTATAGGT

Phenotype

MIM: 603759

Polymorphism

A/G, Transition 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

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