Product Details

SNP ID
rs187018649
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:56091068 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAAAAAAAGAGTGGTTACAGGAATC[C/T]TAGTACTGTACAAGATAAGTCAATA
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 7889 UTR 3 NP_073752.5
XM_005254603.3 7889 UTR 3 XP_005254660.2
XM_011521925.2 7889 UTR 3 XP_011520227.1
XM_017022506.1 7889 UTR 3 XP_016877995.1
XM_017022507.1 7889 UTR 3 XP_016877996.1
XM_017022508.1 7889 UTR 3 XP_016877997.1

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