Product Details

SNP ID
rs142450822
Assay Type
Functionally tested
NCBI dbSNP Submissions
6
Location
Chr.1:24902490 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGGCTGGTGGCCGGCATGCCCGCCA[C/T]GCTGAGGCTGCTGATGCTCGTGCCC
Phenotype
MIM: 600210
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
RUNX3 PubMed Links

Gene Details

Gene
RUNX3
Gene Name
runt related transcription factor 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001031680.2 1291 Missense Mutation ATG,GTG M308V NP_001026850.1
NM_001320672.1 1291 Missense Mutation ATG,GTG M308V NP_001307601.1
NM_004350.2 1291 Missense Mutation ATG,GTG M294V NP_004341.1
XM_005246024.4 1291 Missense Mutation ATG,GTG M308V XP_005246081.1
XM_011542351.1 1291 Missense Mutation ATG,GTG M255V XP_011540653.1
XM_017002670.1 1291 Intron XP_016858159.1

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