Product Details

SNP ID
rs113424988
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:3225156 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGAGGCTTGGTTGCACGCCAGTCTC[A/G]AGAACAGGCTGCATGCAGCCCACTG
Phenotype
MIM: 601337
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
RFX3 PubMed Links

Gene Details

Gene
RFX3
Gene Name
regulatory factor X3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001282116.1 2457 Silent Mutation NP_001269045.1
NM_001282117.1 2457 Intron NP_001269046.1
NM_002919.3 2457 Intron NP_002910.1
NM_134428.2 2457 Silent Mutation NP_602304.1
XM_006716840.1 2457 Silent Mutation XP_006716903.1
XM_006716843.1 2457 Silent Mutation XP_006716906.1
XM_006716844.1 2457 Silent Mutation XP_006716907.1
XM_006716845.2 2457 Silent Mutation XP_006716908.1
XM_006716847.3 2457 Silent Mutation XP_006716910.1
XM_011517998.1 2457 Silent Mutation XP_011516300.1
XM_011517999.1 2457 Silent Mutation XP_011516301.1
XM_011518000.1 2457 Silent Mutation XP_011516302.1
XM_011518001.1 2457 Silent Mutation XP_011516303.1
XM_017015000.1 2457 Silent Mutation XP_016870489.1
XM_017015001.1 2457 Silent Mutation XP_016870490.1
XM_017015002.1 2457 Silent Mutation XP_016870491.1

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