Product Details

SNP ID
rs729833
Assay Type
Functionally tested
NCBI dbSNP Submissions
26
Location
Chr.1:75135460 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CGGCCTCAGTGCAGCTACGCTGGGT[C/T]CCGCGTAGGGAGCGCACCCCAGAAA
Phenotype
MIM: 604425
Polymorphism
C/T, Transition 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 Intron NP_001001933.1
NM_001256114.1 Intron NP_001243043.1
XM_017001316.1 Intron XP_016856805.1
XM_017001317.1 Intron XP_016856806.1

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