Product Details

SNP ID

rs186488928

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:124015173 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTGCCACCTGGGCATCTCGGCCTC[A/G]GAGATGGTGATGCGCGCTCGGGACT

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	974	Silent Mutation	TCA,TCG	S125S	NP_004780.3
XM_006717323.2	974	Silent Mutation	TCA,TCG	S125S	XP_006717386.1

Gene

LOC100505588

Gene Name

uncharacterized LOC100505588

There are no transcripts associated with this gene.

View Full Product Details