Product Details

SNP ID
rs11422
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:43640695 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GCGCTGAGGCAGCCAGGGCTTCAGT[C/T]CCCCATGCTCTTTGGCCATCAGTCC
Phenotype
MIM: 600147
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MEOX1 PubMed Links

Gene Details

Gene
MEOX1
Gene Name
mesenchyme homeobox 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001040002.1 1836 UTR 3 NP_001035091.1
NM_004527.3 1836 UTR 3 NP_004518.1
NM_013999.3 1836 UTR 3 NP_054705.1
XM_011524818.1 1836 Intron XP_011523120.1

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