Product Details

SNP ID

rs148731127

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:124015164 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTGCGCCCGCTGCCACCTGGGCAT[C/T]TCGGCCTCGGAGATGGTGATGCGCG

Phenotype

MIM: 603759

Polymorphism

C/T, 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	965	Silent Mutation	ATC,ATT	I122I	NP_004780.3
XM_006717323.2	965	Silent Mutation	ATC,ATT	I122I	XP_006717386.1

Gene

LOC100505588

Gene Name

uncharacterized LOC100505588

There are no transcripts associated with this gene.

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