Product Details

SNP ID
rs187097765
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.7:144397390 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTCAGGCATCCATGAGAGAGCTGA[C/T]GAAGGCTGCCTGCCCAGAGCCTGGG
Phenotype
MIM: 610934
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
NOBOX PubMed Links

Gene Details

Gene
NOBOX
Gene Name
NOBOX oogenesis homeobox
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001080413.3 2041 Silent Mutation TCA,TCG S642S NP_001073882.3
XM_017011742.1 2041 Silent Mutation TCA,TCG S610S XP_016867231.1

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