Product Details

SNP ID
rs191773270
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:56094234 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCGATGAACAGCAGGGCTCACACTC[C/T]GGCATCTGAAGTTGCTGCTGGCAGA
Phenotype
MIM: 612660
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
RFX7 PubMed Links

Gene Details

Gene
RFX7
Gene Name
regulatory factor X7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_022841.5 4723 Missense Mutation NP_073752.5
XM_005254603.3 4723 Missense Mutation XP_005254660.2
XM_011521925.2 4723 Missense Mutation XP_011520227.1
XM_017022506.1 4723 Missense Mutation XP_016877995.1
XM_017022507.1 4723 Missense Mutation XP_016877996.1
XM_017022508.1 4723 Missense Mutation XP_016877997.1

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