Product Details

SNP ID
rs144617453
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:90058364 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGCAGCGTGGATCAGAATATTGCC[A/G]CTCCTGATTCTGATCCCCTGGGCAG
Phenotype
MIM: 609759
Polymorphism
A/G, 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 1320 Silent Mutation NP_001091643.1
XM_005256274.3 1320 Silent Mutation XP_005256331.1
XM_011522829.1 1320 Missense Mutation XP_011521131.1
XM_011522831.2 1320 Intron XP_011521133.1
XM_017022882.1 1320 Intron XP_016878371.1
XM_017022883.1 1320 Intron XP_016878372.1
XM_017022884.1 1320 Intron XP_016878373.1

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