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WormBase Tree Display for Variation: WBVar01743819

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Name Class

WBVar01743819NamePublic_nameWBVar01743819
Other_namecewivar00443079
CE50507:p.Leu478=
F15B9.7a.1:c.2511G>T
CE42459:p.Leu837=
F15B9.7b.1:c.1434G>T
HGVSgCHROMOSOME_V:g.13025334G>T
Sequence_detailsSMapS_parentSequenceW07G4
Flanking_sequencesCTCATCTCCTTCCATTCAACTTTTTCGACTGACCGCACATCGGGAACTCTTCGTGTCAGC
Mapping_targetW07G4
Source_location225CHROMOSOME_V1302531913025319From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022850From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
WBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
WBStrain00027662From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00001475
TranscriptF15B9.7b.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF15B9.7b.1:c.1434G>T
HGVSpCE50507:p.Leu478=
cDNA_position1434
CDS_position1434
Protein_position478
Exon_number6/21
Codon_changectG/ctT
Amino_acid_changeL
F15B9.7a.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScF15B9.7a.1:c.2511G>T
HGVSpCE42459:p.Leu837=
cDNA_position2538
CDS_position2511
Protein_position837
Exon_number11/27
Codon_changectG/ctT
Amino_acid_changeL
MethodWGS_Flibotte