Product Details

SNP ID
rs113693840
Assay Type
Functionally tested
NCBI dbSNP Submissions
17
Location
Chr.1:197917965 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGATCCAAGACTGAGGCCCGTCTG[A/G]CCAAAGGCGCCCAGCTCAACGGCCG
Phenotype
MIM: 606066
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
LHX9 PubMed Links

Gene Details

Gene
LHX9
Gene Name
LIM homeobox 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001014434.1 885 Missense Mutation ACC,GCC T39A NP_001014434.1
NM_020204.2 885 Missense Mutation ACC,GCC T48A NP_064589.2
XM_005245350.3 885 Missense Mutation ACC,GCC T54A XP_005245407.2
XM_011509781.2 885 Missense Mutation ACC,GCC T54A XP_011508083.2
XM_017001849.1 885 Missense Mutation ACC,GCC T29A XP_016857338.1

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