Product Details

SNP ID

rs28942098

Assay Type

Functionally tested

NCBI dbSNP Submissions

7

Location

Chr.1:193122203 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGGCGGAGGCGAGGGGGGGGAAGAT[A/G]GCGGACGTGCTTAGCGTCCTGCGAC

Phenotype

MIM: 607393

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CDC73 PubMed Links

Gene Details

Gene

CDC73

Gene Name

cell division cycle 73

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024529.4	246	Missense Mutation	ATA,ATG	I1M	NP_078805.3
XM_006711537.3	246	Missense Mutation	ATA,ATG	I1M	XP_006711600.1

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