Product Details

SNP ID
rs202019064
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.12:6570887 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTCCTACCTGCTGTGGGGTAGGTTC[A/G]GGTGCCCGGTTTGCCAGGCGGCTGA
Phenotype
MIM: 603277 MIM: 164031
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
CHD4 PubMed Links

Gene Details

Gene
CHD4
Gene Name
chromodomain helicase DNA binding protein 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001273.3 5807 Silent Mutation CCC,CCT P1901P NP_001264.2
NM_001297553.1 5807 Silent Mutation CCC,CCT P1894P NP_001284482.1
XM_005253668.3 5807 Silent Mutation CCC,CCT P1894P XP_005253725.1
XM_006718958.1 5807 Silent Mutation CCC,CCT P1929P XP_006719021.1
XM_006718959.1 5807 Silent Mutation CCC,CCT P1904P XP_006719022.1
XM_006718960.1 5807 Silent Mutation CCC,CCT P1903P XP_006719023.1
XM_006718961.2 5807 Silent Mutation CCC,CCT P1897P XP_006719024.1
XM_006718962.1 5807 Silent Mutation CCC,CCT P1891P XP_006719025.1
XM_017018725.1 5807 Silent Mutation CCC,CCT P1903P XP_016874214.1
XM_017018726.1 5807 Silent Mutation CCC,CCT P1902P XP_016874215.1
XM_017018727.1 5807 Silent Mutation CCC,CCT P1901P XP_016874216.1
XM_017018728.1 5807 Silent Mutation CCC,CCT P1900P XP_016874217.1
XM_017018729.1 5807 Silent Mutation CCC,CCT P1895P XP_016874218.1
XM_017018730.1 5807 Silent Mutation CCC,CCT P1889P XP_016874219.1
XM_017018731.1 5807 Silent Mutation CCC,CCT P1888P XP_016874220.1
XM_017018732.1 5807 Silent Mutation CCC,CCT P1884P XP_016874221.1
XM_017018733.1 5807 Silent Mutation CCC,CCT P1882P XP_016874222.1
XM_017018734.1 5807 Silent Mutation CCC,CCT P1881P XP_016874223.1
Gene
NOP2
Gene Name
NOP2 nucleolar protein
There are no transcripts associated with this gene.

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