Product Details

SNP ID
rs181660659
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:70197301 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACTTCTTAATCTTAATAATGGTCAA[C/T]TTTTGCCACTACAACTTCAGGTACC
Phenotype
MIM: 614843
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
ODAM PubMed Links

Gene Details

Gene
ODAM
Gene Name
odontogenic, ameloblast asssociated
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_017855.3 138 Missense Mutation CTT,TTT L41F NP_060325.3
XM_005265698.3 138 Missense Mutation CTT,TTT L58F XP_005265755.1
XM_006714245.3 138 Missense Mutation CTT,TTT L58F XP_006714308.1
XM_017008331.1 138 Missense Mutation CTT,TTT L27F XP_016863820.1

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