Product Details

SNP ID
rs142209700
Assay Type
Functionally tested
NCBI dbSNP Submissions
2
Location
Chr.1:112689038 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCGGGTCAGGTTCTTCAGACTCGAC[C/T]GCTGGGCCGACGTGCGGTTCCCAGA
Phenotype
MIM: 610742
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MOV10 PubMed Links

Gene Details

Gene
MOV10
Gene Name
Mov10 RISC complex RNA helicase
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001130079.2 1488 Missense Mutation CGC,TGC R81C NP_001123551.1
NM_001286072.1 1488 Missense Mutation CGC,TGC R25C NP_001273001.1
NM_001321324.1 1488 Missense Mutation CGC,TGC R81C NP_001308253.1
NM_020963.4 1488 Missense Mutation CGC,TGC R81C NP_066014.1
XM_005270869.4 1488 Missense Mutation CGC,TGC R25C XP_005270926.1
XM_005270870.4 1488 Missense Mutation CGC,TGC R25C XP_005270927.1
XM_017001318.1 1488 Missense Mutation CGC,TGC R25C XP_016856807.1
XM_017001319.1 1488 Missense Mutation CGC,TGC R81C XP_016856808.1

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