Product Details

SNP ID
rs12683269
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:3220888 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ATACTAGGATTCCATTAATTGATTC[A/G]TTCTAACCATATACATGGAGGTTGT
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 6725 UTR 3 NP_001269045.1
NM_001282117.1 6725 Intron NP_001269046.1
NM_002919.3 6725 Intron NP_002910.1
NM_134428.2 6725 UTR 3 NP_602304.1
XM_006716840.1 6725 UTR 3 XP_006716903.1
XM_006716843.1 6725 UTR 3 XP_006716906.1
XM_006716844.1 6725 UTR 3 XP_006716907.1
XM_006716845.2 6725 Intron XP_006716908.1
XM_006716847.3 6725 UTR 3 XP_006716910.1
XM_011517998.1 6725 UTR 3 XP_011516300.1
XM_011517999.1 6725 UTR 3 XP_011516301.1
XM_011518000.1 6725 UTR 3 XP_011516302.1
XM_011518001.1 6725 UTR 3 XP_011516303.1
XM_017015000.1 6725 UTR 3 XP_016870489.1
XM_017015001.1 6725 UTR 3 XP_016870490.1
XM_017015002.1 6725 UTR 3 XP_016870491.1

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