Product Details

SNP ID

rs17199

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.7:15612145 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

ACATACCTGCTCACTGCCATACGCA[C/T]GACCAAACACATCTGGAATATTCAA

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	1438	UTR 3			NP_005915.2

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