Product Details

SNP ID
rs10014077
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:4862503 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAGTTTCTTCATTTGCAAAAAGTAG[A/G]CAGGAACTTCTCCCCTGCGGGGTTG
Phenotype
MIM: 142983
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
MSX1 PubMed Links

Gene Details

Gene
MSX1
Gene Name
msh homeobox 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_002448.3 Intron NP_002439.2

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