Product Details

SNP ID
rs188196919
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:56094617 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGGACTACTTGAGACAATGCTGGC[A/G]TCATGATATGCCATACTGGAGCTTA
Phenotype
MIM: 612660
Polymorphism
A/G, 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 4340 Silent Mutation GAC,GAT D1037D NP_073752.5
XM_005254603.3 4340 Silent Mutation GAC,GAT D1037D XP_005254660.2
XM_011521925.2 4340 Silent Mutation GAC,GAT D940D XP_011520227.1
XM_017022506.1 4340 Silent Mutation GAC,GAT D1037D XP_016877995.1
XM_017022507.1 4340 Silent Mutation GAC,GAT D940D XP_016877996.1
XM_017022508.1 4340 Silent Mutation GAC,GAT D940D XP_016877997.1

View Full Product Details