Product Details

SNP ID
rs28667468
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.16:90059858 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCGTACGGTTCCCTAATTCACAAGT[C/T]ATCTGTTCAAGAGCAGTTTTTTTGA
Phenotype
MIM: 609759
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
PRDM7 PubMed Links

Gene Details

Gene
PRDM7
Gene Name
PR domain 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001098173.1 Intron NP_001091643.1
XM_005256274.3 Intron XP_005256331.1
XM_011522829.1 Intron XP_011521131.1
XM_011522831.2 Intron XP_011521133.1
XM_017022882.1 Intron XP_016878371.1
XM_017022883.1 Intron XP_016878372.1
XM_017022884.1 Intron XP_016878373.1

View Full Product Details