Product Details

SNP ID

rs2237493

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.7:15612443 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

CTGTCGTGACTGTCTTCATTTGCTA[G/T]AGAGTCCCCTGTTTGCTGGAGGGTG

Phenotype

MIM: 600535

Polymorphism

G/T, Transversion 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	1140	Missense Mutation			NP_005915.2

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