Product Details

SNP ID
rs111241943
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:42101921 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTGAGCACTGGCAGCTTCACTGAC[C/T]TGTAGATCATCTGCAGACCCCAGAC
Phenotype
MIM: 608588
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
DHX58 PubMed Links

Gene Details

Gene
DHX58
Gene Name
DEXH-box helicase 58
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_024119.2 2096 Missense Mutation AAG,AGG K626R NP_077024.2
XM_017025059.1 2096 Missense Mutation AAG,AGG K626R XP_016880548.1
XM_017025060.1 2096 Missense Mutation AAG,AGG K626R XP_016880549.1

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