Product Details

SNP ID

rs116937127

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:144397378 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGGTCTGGCCCCTTCAGGCATCCA[C/T]GAGAGAGCTGACGAAGGCTGCCTGC

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	2053	Silent Mutation	TCA,TCG	S646S	NP_001073882.3
XM_017011742.1	2053	Silent Mutation	TCA,TCG	S614S	XP_016867231.1

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