Product Details

SNP ID

hCV8921343

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:6570131 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCAATTTTCATCAAGAAATTTGCTG[G/T]GGTTTTTTATGCTTTTGGTTTTTTC

Phenotype

MIM: 603277 MIM: 164031

Polymorphism

G/T, Transversion 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	6341	UTR 3			NP_001264.2
NM_001297553.1	6341	UTR 3			NP_001284482.1

Gene

NOP2

Gene Name

NOP2 nucleolar protein

There are no transcripts associated with this gene.

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