Product Details

SNP ID
rs199550783
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:70198056 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGCTGGACTGCTCCCAAATCAGATA[C/T]CCTTAACAGGAGAGGCCAGTTTTGC
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_017855.3 291 Missense Mutation CCC,TCC P92S NP_060325.3
XM_005265698.3 291 Missense Mutation CCC,TCC P109S XP_005265755.1
XM_006714245.3 291 Missense Mutation CCC,TCC P109S XP_006714308.1
XM_017008331.1 291 Missense Mutation CCC,TCC P78S XP_016863820.1

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