Product Details

SNP ID
rs150792046
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:43642010 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTCACACGCTTCCACTTCATCCTT[C/T]GGTTCTGGAACCACACTTTGACCTG
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 1096 Missense Mutation CAA,CGA Q107R NP_001035091.1
NM_004527.3 1096 Missense Mutation CAA,CGA Q222R NP_004518.1
NM_013999.3 1096 Silent Mutation CCA,CCG P164P NP_054705.1
XM_011524818.1 1096 Missense Mutation AAA,GAA K226E XP_011523120.1

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