Product Details

SNP ID
rs73274785
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:68422577 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CACTCTTATTCTGCTCCAGCCTCTT[C/G]AATAAGCTTTCACTCATGCCAAGAG
Phenotype
MIM: 601810
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
DNA2 PubMed Links

Gene Details

Gene
DNA2
Gene Name
DNA replication helicase/nuclease 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001080449.2 1928 Silent Mutation TTC,TTG F810L NP_001073918.2
XM_006717680.3 1928 Silent Mutation TTC,TTG F840L XP_006717743.1
XM_011539417.1 1928 Silent Mutation TTC,TTG F450L XP_011537719.1
XM_017015799.1 1928 Silent Mutation TTC,TTG F586L XP_016871288.1

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