Product Details

SNP ID

rs189306575

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:144399799 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGGCCAGGGGCTGCAGGATTGTCC[G/T]TGCTTTCTTTCCCATTCAGTTTCTC

Phenotype

MIM: 610934

Polymorphism

G/T, Transversion 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	1227	Missense Mutation	AAG,ACG	K371T	NP_001073882.3
XM_017011742.1	1227	Missense Mutation	AAG,ACG	K339T	XP_016867231.1

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