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SNP ID

rs17764770

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:162267800 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCATAACTTCTTTCAAGTCTGTTGG[C/T]TATATTAACTTGACTTTAGTTGTTC

Phenotype

MIM: 606951

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

IFIH1 PubMed Links

Gene Details

Gene

IFIH1

Gene Name

interferon induced with helicase C domain 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_022168.3		Intron			NP_071451.2

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