Product Details

SNP ID
rs6955921
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:15614670 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTCCTTTATTAATTTTTCTATAGTT[G/T]TGATAAAACCACATTATCTTATTAA
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 Intron NP_005915.2

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