Product Details

SNP ID
rs16950113
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:48920219 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CCAATGAGAATGCTTCTCTTGTTCA[C/T]TTAAACCTTTGTAGTTAGAAAAATA
Phenotype
MIM: 602932
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SMAD7 PubMed Links

Gene Details

Gene
SMAD7
Gene Name
SMAD family member 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001190821.1 2019 UTR 3 NP_001177750.1
NM_001190822.1 2019 UTR 3 NP_001177751.1
NM_001190823.1 2019 UTR 3 NP_001177752.1
NM_005904.3 2019 UTR 3 NP_005895.1

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