Product Details

SNP ID

rs7897488

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:68419989 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAAGACTATACTACCGACTTGGAGA[G/T]GAAAAATAGCTTTGTCTAAAAGATG

Phenotype

MIM: 601810

Polymorphism

G/T, 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		Intron			NP_001073918.2
XM_006717680.3		Intron			XP_006717743.1
XM_011539417.1		Intron			XP_011537719.1
XM_017015799.1		Intron			XP_016871288.1

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