Product Details

SNP ID
rs9628282
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:50096523 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AGAGAATTGCTGGGCTGTATGGTAA[G/T]TCTAGGTTTAACTTTGTGAGGAACC
Phenotype
MIM: 605794
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
MOV10L1 PubMed Links

Gene Details

Gene
MOV10L1
Gene Name
Mov10 RISC complex RNA helicase like 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001164104.1 Intron NP_001157576.1
NM_001164105.1 Intron NP_001157577.1
NM_001164106.1 Intron NP_001157578.1
NM_018995.2 Intron NP_061868.1
XM_005261923.3 Intron XP_005261980.1
XM_011530696.1 Intron XP_011528998.1
XM_011530697.1 Intron XP_011528999.1
XM_011530698.1 Intron XP_011529000.1
XM_011530699.1 Intron XP_011529001.1
XM_011530700.2 Intron XP_011529002.1
XM_011530701.1 Intron XP_011529003.1
XM_011530702.1 Intron XP_011529004.1
XM_011530703.1 Intron XP_011529005.1
XM_011530704.1 Intron XP_011529006.1
XM_017028833.1 Intron XP_016884322.1
XM_017028834.1 Intron XP_016884323.1
XM_017028835.1 Intron XP_016884324.1
XM_017028836.1 Intron XP_016884325.1
XM_017028837.1 Intron XP_016884326.1

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