Product Details

SNP ID

rs199946428

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.18:57436703 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTCGCAGGTGGCCACGTCGGGCCA[G/T]CTGGAAGAAATCAACACCAAAGAGG

Phenotype

MIM: 604894

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

ONECUT2 PubMed Links

Gene Details

Gene

ONECUT2

Gene Name

one cut homeobox 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004852.2	1284	Missense Mutation	CAG,CAT	Q329H	NP_004843.2
XM_017026096.1	1284	Missense Mutation	CAG,CAT	Q329H	XP_016881585.1

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