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WormBase Tree Display for Variation: WBVar01643942

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Name Class

WBVar01643942NamePublic_nameWBVar01643942
Other_namecewivar00330015
C46F11.1a.1:c.1329G>A
C46F11.1b.1:c.1314G>A
CE30906:p.Gln443=
CE37957:p.Gln438=
HGVSgCHROMOSOME_III:g.3647063G>A
Sequence_detailsSMapS_parentSequenceC46F11
Flanking_sequencesGGCGGAGAGCAATCTTGCTCGGCCACCACAAAAGTTTATGTAGCAGGTGAGCCTACATAC
Mapping_targetC46F11
Source_location225CHROMOSOME_III36470453647045From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006629From_analysisMillion_mutation_project_reanalysis
WBStrain00006637From_analysisMillion_mutation_project_reanalysis
WBStrain00023018From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
WBStrain00023191From_analysisMillion_mutation_project_reanalysis
WBStrain00024204From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006822
TranscriptC46F11.1b.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC46F11.1b.1:c.1314G>A
HGVSpCE37957:p.Gln438=
cDNA_position1317
CDS_position1314
Protein_position438
Exon_number11/17
Codon_changecaG/caA
Amino_acid_changeQ
C46F11.1a.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScC46F11.1a.1:c.1329G>A
HGVSpCE30906:p.Gln443=
cDNA_position1329
CDS_position1329
Protein_position443
Exon_number10/17
Codon_changecaG/caA
Amino_acid_changeQ
MethodWGS_Flibotte