Product Details

SNP ID

rs6970492

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:15615540 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTAAATATGACACTATTTTCCTGTA[C/T]TATAATTTAGGTAATTACGCTACTG

Phenotype

MIM: 600535

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MEOX2 PubMed Links

Gene Details

Gene

MEOX2

Gene Name

mesenchyme homeobox 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005924.4		Intron			NP_005915.2

View Full Product Details