Product Details

SNP ID
rs2525702
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:144398975 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTTGTCCCCCAGGACCCACAGGGGC[C/T]GTCCTTGTGGCTGCTGTCACTGCCA
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 1559 Missense Mutation AGC,GGC S482G NP_001073882.3
XM_017011742.1 1559 Missense Mutation AGC,GGC S450G XP_016867231.1

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