Product Details

SNP ID: rs199805211
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.9:136209015 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGTGGACGGACGCTCTGGGTGTCTC[A/G]GTCTCCATGGGACACCTCTGGGGGA
Phenotype: MIM: 600577 MIM: 612860
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: LHX3 PubMed Links

Gene Details

There are no transcripts associated with this gene.

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_181701.3	1848	Missense Mutation			NP_859052.3