Product Details

SNP ID
rs116590034
Assay Type
Functionally tested
NCBI dbSNP Submissions
21
Location
Chr.1:75136615 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCTACTCCGCAGTGTCAGGGGCTC[A/C]TGTCAGAGGAGTGCGGGCGGACTAC
Phenotype
MIM: 604425
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
LHX8 PubMed Links

Gene Details

Gene
LHX8
Gene Name
LIM homeobox 8
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001001933.1 86 Missense Mutation ATG,CTG M11L NP_001001933.1
NM_001256114.1 86 Missense Mutation ATG,CTG M1L NP_001243043.1
XM_017001316.1 86 Missense Mutation ATG,CTG M1L XP_016856805.1
XM_017001317.1 86 Missense Mutation ATG,CTG M1L XP_016856806.1

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