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WormBase Tree Display for Variation: WBVar01604532

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Name Class

WBVar01604532NamePublic_nameWBVar01604532
Other_namecewivar00281219
F26C11.1.1:c.117A>T
F26C11.1.2:c.117A>T
CE01559:p.Gly39=
HGVSgCHROMOSOME_II:g.9895767A>T
Sequence_detailsSMapS_parentSequenceF26C11
Flanking_sequencesATTTTCAAACTTTCAGATTTGGCGGCATGGGATCGTTCCGCGCTAGAAGGATTATTCCCG
Mapping_targetF26C11
Source_location225CHROMOSOME_II98957089895708From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006622From_analysisMillion_mutation_project_reanalysis
WBStrain00022852From_analysisMillion_mutation_project_reanalysis
WBStrain00022856From_analysisMillion_mutation_project_reanalysis
WBStrain00022902From_analysisMillion_mutation_project_reanalysis
WBStrain00022930From_analysisMillion_mutation_project_reanalysis
WBStrain00023018From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
WBStrain00023191From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00009146
TranscriptF26C11.1.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF26C11.1.1:c.117A>T
HGVSpCE01559:p.Gly39=
cDNA_position124
CDS_position117
Protein_position39
Exon_number3/10
Codon_changeggA/ggT
Amino_acid_changeG
F26C11.1.2VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF26C11.1.2:c.117A>T
HGVSpCE01559:p.Gly39=
cDNA_position214
CDS_position117
Protein_position39
Exon_number4/11
Codon_changeggA/ggT
Amino_acid_changeG
MethodWGS_Flibotte