Product Details

SNP ID
rs137899630
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:3225104 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTCTGATAGTCTGAGTACTTGTGA[C/T]AATGTGCTCGCTGTGAATTGGATTC
Phenotype
MIM: 601337
Polymorphism
C/T, 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 2509 Missense Mutation NP_001269045.1
NM_001282117.1 2509 Intron NP_001269046.1
NM_002919.3 2509 Intron NP_002910.1
NM_134428.2 2509 Missense Mutation NP_602304.1
XM_006716840.1 2509 Missense Mutation XP_006716903.1
XM_006716843.1 2509 Missense Mutation XP_006716906.1
XM_006716844.1 2509 Missense Mutation XP_006716907.1
XM_006716845.2 2509 Missense Mutation XP_006716908.1
XM_006716847.3 2509 Missense Mutation XP_006716910.1
XM_011517998.1 2509 Missense Mutation XP_011516300.1
XM_011517999.1 2509 Missense Mutation XP_011516301.1
XM_011518000.1 2509 Missense Mutation XP_011516302.1
XM_011518001.1 2509 Missense Mutation XP_011516303.1
XM_017015000.1 2509 Missense Mutation XP_016870489.1
XM_017015001.1 2509 Missense Mutation XP_016870490.1
XM_017015002.1 2509 Missense Mutation XP_016870491.1

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