Product Details

SNP ID
rs115092272
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.15:56245793 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AATGCAGGAGCCAAAATTTGAGTCC[C/T]GGAAGTTTAATTCCAGAGCCTGCAA
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 1862 Intron NP_073752.5
XM_005254603.3 1862 Intron XP_005254660.2
XM_011521925.2 1862 Intron XP_011520227.1
XM_017022506.1 1862 UTR 5 XP_016877995.1
XM_017022507.1 1862 Intron XP_016877996.1
XM_017022508.1 1862 Intron XP_016877997.1
Gene
TEX9
Gene Name
testis expressed 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286449.1 1862 Intron NP_001273378.1
NM_198524.2 1862 Intron NP_940926.1
XM_005254359.4 1862 Intron XP_005254416.1
XM_005254361.3 1862 Intron XP_005254418.1
XM_011521530.2 1862 Intron XP_011519832.1
XM_017022160.1 1862 Intron XP_016877649.1
XM_017022161.1 1862 Intron XP_016877650.1
XM_017022162.1 1862 Intron XP_016877651.1
XM_017022163.1 1862 Intron XP_016877652.1
XM_017022164.1 1862 Intron XP_016877653.1
XM_017022166.1 1862 Intron XP_016877655.1
XM_017022167.1 1862 Intron XP_016877656.1

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