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SNP ID

rs10057302

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:157087601 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTATCAAGATGTCTGCAATTATGTA[A/C]ACATTTAGATTTTCAAAAAATGGGC

Phenotype

MIM: 606652

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

HAVCR2 PubMed Links

Gene Details

Gene

HAVCR2

Gene Name

hepatitis A virus cellular receptor 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032782.4		Intron			NP_116171.3

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