Product Details

SNP ID
rs2713933
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:56246364 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GAGACCTTATTGCCAGAGTGAGATA[A/C]CCTTTCAGGGAGGAAAGGGGCAGCC
Phenotype
MIM: 612660
Polymorphism
A/C, Transversion 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 1291 Intron NP_073752.5
XM_005254603.3 1291 Intron XP_005254660.2
XM_011521925.2 1291 Intron XP_011520227.1
XM_017022506.1 1291 UTR 5 XP_016877995.1
XM_017022507.1 1291 Intron XP_016877996.1
XM_017022508.1 1291 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 1291 Intron NP_001273378.1
NM_198524.2 1291 Intron NP_940926.1
XM_005254359.4 1291 Intron XP_005254416.1
XM_005254361.3 1291 Intron XP_005254418.1
XM_011521530.2 1291 Intron XP_011519832.1
XM_017022160.1 1291 Intron XP_016877649.1
XM_017022161.1 1291 Intron XP_016877650.1
XM_017022162.1 1291 Intron XP_016877651.1
XM_017022163.1 1291 Intron XP_016877652.1
XM_017022164.1 1291 Intron XP_016877653.1
XM_017022166.1 1291 Intron XP_016877655.1
XM_017022167.1 1291 Intron XP_016877656.1

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