Product Details

SNP ID
rs111625995
Assay Type
Functionally tested
NCBI dbSNP Submissions
2
Location
Chr.1:24902269 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGTTGCCGGCGGCGACAGAGGCAGC[C/G]CTGCTGGTGCAAGAGGCCAGCATGC
Phenotype
MIM: 600210
Polymorphism
C/G, 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 1512 Silent Mutation AGC,AGG S381R NP_001026850.1
NM_001320672.1 1512 Silent Mutation AGC,AGG S381R NP_001307601.1
NM_004350.2 1512 Silent Mutation AGC,AGG S367R NP_004341.1
XM_005246024.4 1512 Silent Mutation AGC,AGG S381R XP_005246081.1
XM_011542351.1 1512 Silent Mutation AGC,AGG S328R XP_011540653.1
XM_017002670.1 1512 Intron XP_016858159.1

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