Product Details

SNP ID
rs78810959
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:56247527 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAGGGAGTAACATGAGCACTGGTGT[A/G]AAGCCATGAAAGGGTACTGTTTGCT
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_022841.5 128 Intron NP_073752.5
XM_005254603.3 128 Intron XP_005254660.2
XM_011521925.2 128 Intron XP_011520227.1
XM_017022506.1 128 UTR 5 XP_016877995.1
XM_017022507.1 128 Intron XP_016877996.1
XM_017022508.1 128 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_001286449.1 128 Intron NP_001273378.1
NM_198524.2 128 Intron NP_940926.1
XM_005254359.4 128 Intron XP_005254416.1
XM_005254361.3 128 Intron XP_005254418.1
XM_011521530.2 128 Intron XP_011519832.1
XM_017022160.1 128 Intron XP_016877649.1
XM_017022161.1 128 Intron XP_016877650.1
XM_017022162.1 128 Intron XP_016877651.1
XM_017022163.1 128 Intron XP_016877652.1
XM_017022164.1 128 Intron XP_016877653.1
XM_017022166.1 128 Intron XP_016877655.1
XM_017022167.1 128 Intron XP_016877656.1

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