Product Details

SNP ID

rs144550882

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:6570917 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCGGTTTGCCAGGCGGCTGAGAAT[A/G]TTACGCTCTGACATCTGTAACCTCA

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	5777	Silent Mutation	AAC,AAT	N1891N	NP_001264.2
NM_001297553.1	5777	Silent Mutation	AAC,AAT	N1884N	NP_001284482.1
XM_005253668.3	5777	Silent Mutation	AAC,AAT	N1884N	XP_005253725.1
XM_006718958.1	5777	Silent Mutation	AAC,AAT	N1919N	XP_006719021.1
XM_006718959.1	5777	Silent Mutation	AAC,AAT	N1894N	XP_006719022.1
XM_006718960.1	5777	Silent Mutation	AAC,AAT	N1893N	XP_006719023.1
XM_006718961.2	5777	Silent Mutation	AAC,AAT	N1887N	XP_006719024.1
XM_006718962.1	5777	Silent Mutation	AAC,AAT	N1881N	XP_006719025.1
XM_017018725.1	5777	Silent Mutation	AAC,AAT	N1893N	XP_016874214.1
XM_017018726.1	5777	Silent Mutation	AAC,AAT	N1892N	XP_016874215.1
XM_017018727.1	5777	Silent Mutation	AAC,AAT	N1891N	XP_016874216.1
XM_017018728.1	5777	Silent Mutation	AAC,AAT	N1890N	XP_016874217.1
XM_017018729.1	5777	Silent Mutation	AAC,AAT	N1885N	XP_016874218.1
XM_017018730.1	5777	Silent Mutation	AAC,AAT	N1879N	XP_016874219.1
XM_017018731.1	5777	Silent Mutation	AAC,AAT	N1878N	XP_016874220.1
XM_017018732.1	5777	Silent Mutation	AAC,AAT	N1874N	XP_016874221.1
XM_017018733.1	5777	Silent Mutation	AAC,AAT	N1872N	XP_016874222.1
XM_017018734.1	5777	Silent Mutation	AAC,AAT	N1871N	XP_016874223.1

Gene

NOP2

Gene Name

NOP2 nucleolar protein

There are no transcripts associated with this gene.

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