Product Details

SNP ID
rs1792671
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:47835823 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTGTTCAATAAATTACCATCTTTAA[C/T]TAAAAATAAGTAAATCAAAGAGCAT
Phenotype
MIM: 601366
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SMAD2 PubMed Links

Gene Details

Gene
SMAD2
Gene Name
SMAD family member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001003652.3 7700 UTR 3 NP_001003652.1
NM_001135937.2 7700 UTR 3 NP_001129409.1
NM_005901.5 7700 UTR 3 NP_005892.1
XM_005258259.3 7700 UTR 3 XP_005258316.1
XM_006722451.3 7700 UTR 3 XP_006722514.1
XM_011525984.2 7700 UTR 3 XP_011524286.1
XM_011525985.2 7700 UTR 3 XP_011524287.1
XM_017025745.1 7700 UTR 3 XP_016881234.1
XM_017025746.1 7700 UTR 3 XP_016881235.1
XM_017025747.1 7700 UTR 3 XP_016881236.1
XM_017025748.1 7700 UTR 3 XP_016881237.1
XM_017025749.1 7700 Intron XP_016881238.1
XM_017025750.1 7700 UTR 3 XP_016881239.1

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