Product Details

SNP ID
rs139118373
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:49973260 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCTGGCAGCGCAGCTCGGCCTCAC[C/G]CAGACCCAGGTGGGGCCAGTGTCGT
Phenotype
MIM: 601911
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
DLX4 PubMed Links

Gene Details

Gene
DLX4
Gene Name
distal-less homeobox 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001934.3 788 Silent Mutation ACC,ACG T85T NP_001925.2
NM_138281.2 788 Silent Mutation ACC,ACG T157T NP_612138.1
XM_017024291.1 788 Silent Mutation ACC,ACG T85T XP_016879780.1

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