Product Details

SNP ID
rs148254134
Assay Type
Functionally tested
NCBI dbSNP Submissions
3
Location
Chr.1:24902251 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCAGGCTGGGGTTCATGAGGTTGCC[G/T]GCGGCGACAGAGGCAGCGCTGCTGG
Phenotype
MIM: 600210
Polymorphism
G/T, Transversion 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 1530 Silent Mutation NP_001026850.1
NM_001320672.1 1530 Silent Mutation NP_001307601.1
NM_004350.2 1530 Silent Mutation NP_004341.1
XM_005246024.4 1530 Silent Mutation XP_005246081.1
XM_011542351.1 1530 Silent Mutation XP_011540653.1
XM_017002670.1 1530 Intron XP_016858159.1

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