Product Details

SNP ID
rs150998602
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:56245023 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTTTGGGCCCGTGGGTGTTATGAG[C/T]CCTTCAGCTTTAACTTTTCTGATAG
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 2632 Intron NP_073752.5
XM_005254603.3 2632 Intron XP_005254660.2
XM_011521925.2 2632 Intron XP_011520227.1
XM_017022506.1 2632 UTR 5 XP_016877995.1
XM_017022507.1 2632 Intron XP_016877996.1
XM_017022508.1 2632 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 2632 Intron NP_001273378.1
NM_198524.2 2632 Intron NP_940926.1
XM_005254359.4 2632 Intron XP_005254416.1
XM_005254361.3 2632 Intron XP_005254418.1
XM_011521530.2 2632 Intron XP_011519832.1
XM_017022160.1 2632 Intron XP_016877649.1
XM_017022161.1 2632 Intron XP_016877650.1
XM_017022162.1 2632 Intron XP_016877651.1
XM_017022163.1 2632 Intron XP_016877652.1
XM_017022164.1 2632 Intron XP_016877653.1
XM_017022166.1 2632 Intron XP_016877655.1
XM_017022167.1 2632 Intron XP_016877656.1

View Full Product Details