Product Details

SNP ID
rs527800
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:3220262 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AGATTCTCTTAATCCACTCGAACTC[C/G]TTTCTTCCTAAGGCTTTACTTACAC
Phenotype
MIM: 601337
Polymorphism
C/G, 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 7351 UTR 3 NP_001269045.1
NM_001282117.1 7351 Intron NP_001269046.1
NM_002919.3 7351 Intron NP_002910.1
NM_134428.2 7351 UTR 3 NP_602304.1
XM_006716840.1 7351 UTR 3 XP_006716903.1
XM_006716843.1 7351 UTR 3 XP_006716906.1
XM_006716844.1 7351 UTR 3 XP_006716907.1
XM_006716845.2 7351 Intron XP_006716908.1
XM_006716847.3 7351 UTR 3 XP_006716910.1
XM_011517998.1 7351 UTR 3 XP_011516300.1
XM_011517999.1 7351 UTR 3 XP_011516301.1
XM_011518000.1 7351 UTR 3 XP_011516302.1
XM_011518001.1 7351 UTR 3 XP_011516303.1
XM_017015000.1 7351 UTR 3 XP_016870489.1
XM_017015001.1 7351 UTR 3 XP_016870490.1
XM_017015002.1 7351 UTR 3 XP_016870491.1

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