Product Details

SNP ID
rs141009772
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:116882376 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCATCTTTCTTTTTAGACAATTCGC[C/G]AGAAGTTTCCCCTCCTAACAACAAG
Phenotype
MIM: 612659
Polymorphism
C/G, Transversion 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_173560.3 577 Missense Mutation CAG,GAG Q172E NP_775831.2
XM_011535589.1 577 Missense Mutation CAG,GAG Q172E XP_011533891.1
XM_017010477.1 577 Missense Mutation CAG,GAG Q46E XP_016865966.1

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