Product Details

SNP ID
rs684434
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:3226462 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ATGGCTGTACAGTGTACAGCCACCA[G/T]GAGCAAGGTCTGAGAAATGGCAATT
Phenotype
MIM: 601337
Polymorphism
G/T, Transversion 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 Intron NP_001269045.1
NM_001282117.1 Intron NP_001269046.1
NM_002919.3 Intron NP_002910.1
NM_134428.2 Intron NP_602304.1
XM_006716840.1 Intron XP_006716903.1
XM_006716843.1 Intron XP_006716906.1
XM_006716844.1 Intron XP_006716907.1
XM_006716845.2 Intron XP_006716908.1
XM_006716847.3 Intron XP_006716910.1
XM_011517998.1 Intron XP_011516300.1
XM_011517999.1 Intron XP_011516301.1
XM_011518000.1 Intron XP_011516302.1
XM_011518001.1 Intron XP_011516303.1
XM_017015000.1 Intron XP_016870489.1
XM_017015001.1 Intron XP_016870490.1
XM_017015002.1 Intron XP_016870491.1

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