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WormBase Tree Display for Variation: WBVar01911513

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Name Class

WBVar01911513NamePublic_nameWBVar01911513
Other_namecewivar00627534
CE50184:p.Val57=
CE30703:p.Val165=
W10C8.4d.1:c.171C>T
CE50143:p.Val118=
W10C8.4c.1:c.354C>T
W10C8.4a.1:c.495C>T
HGVSgCHROMOSOME_I:g.2852174G>A
Sequence_detailsSMapS_parentSequenceW10C8
Flanking_sequencesGCACTGCTGACACCGAGTTAGAAACTCGACACAGCGATGTCAGCCCATGAATATCGATCT
Mapping_targetW10C8
Source_location225CHROMOSOME_I28521762852176From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00031113From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00021127
TranscriptW10C8.4c.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScW10C8.4c.1:c.354C>T
HGVSpCE50143:p.Val118=
cDNA_position354
CDS_position354
Protein_position118
Exon_number4/4
Codon_changegtC/gtT
Amino_acid_changeV
W10C8.4a.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScW10C8.4a.1:c.495C>T
HGVSpCE30703:p.Val165=
cDNA_position602
CDS_position495
Protein_position165
Exon_number6/7
Codon_changegtC/gtT
Amino_acid_changeV
W10C8.4d.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScW10C8.4d.1:c.171C>T
HGVSpCE50184:p.Val57=
cDNA_position171
CDS_position171
Protein_position57
Exon_number2/2
Codon_changegtC/gtT
Amino_acid_changeV
MethodWGS_Flibotte