Product Details

SNP ID
rs17853900
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:116877291 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCCAGGAGGATGGCCAAGGTCCCG[A/G]AGCTGGAAGACACCTTCCTGCAGGC
Phenotype
MIM: 612659
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
RFX6 PubMed Links

Gene Details

Gene
RFX6
Gene Name
regulatory factor X6
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_173560.3 79 Missense Mutation AAG,GAG K6E NP_775831.2
XM_011535589.1 79 Missense Mutation AAG,GAG K6E XP_011533891.1
XM_017010477.1 79 Intron XP_016865966.1

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