Product Details

SNP ID

rs139972728

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:23681561 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCAGCTCGGGAGCGCTTCTGCGGC[G/T]GCTTAGGGGTTTGGGGAAGCCTTGG

Phenotype

MIM: 602041

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

NKX3-1 PubMed Links

Gene Details

Gene

NKX3-1

Gene Name

NK3 homeobox 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256339.1	413	Missense Mutation	CAG,CCG	Q47P	NP_001243268.1
NM_006167.3	413	Missense Mutation	CAG,CCG	Q122P	NP_006158.2

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