Product Details

SNP ID
rs145195318
Assay Type
Functionally tested
NCBI dbSNP Submissions
1
Location
Chr.1:75137144 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGACGAGGACTCGTGCTCCTCCTC[C/G]GCCCCGCTGTCCCCGTCGTCCTCGC
Phenotype
MIM: 604425
Polymorphism
C/G, 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_001001933.1 205 Silent Mutation TCC,TCG S50S NP_001001933.1
NM_001256114.1 205 Silent Mutation TCC,TCG S40S NP_001243043.1
XM_017001316.1 205 Silent Mutation TCC,TCG S40S XP_016856805.1
XM_017001317.1 205 Silent Mutation TCC,TCG S40S XP_016856806.1

View Full Product Details