Product Details

SNP ID
rs137854505
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:136198755 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTTCATGTTGCGGAAATACTGCCC[T/C]CAGCGCTGCCGGCCGGCGTCCTTCT
Phenotype
MIM: 600577 MIM: 612860
Polymorphism
T/C, Transition substitution
Allele Nomenclature
Literature Links
LHX3 PubMed Links

Gene Details

Gene
LHX3
Gene Name
LIM homeobox 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_014564.4 1103 Nonsense Mutation TGA,TGG *229W NP_055379.1
NM_178138.5 1103 Nonsense Mutation TGA,TGG *224W NP_835258.1
XM_005263410.1 1103 Nonsense Mutation TGA,TGG *213W XP_005263467.1
XM_017015168.1 1103 Nonsense Mutation TGA,TGG *200W XP_016870657.1
Gene
QSOX2
Gene Name
quiescin sulfhydryl oxidase 2
There are no transcripts associated with this gene.

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