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WormBase Tree Display for Variation: WBVar01729839

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Name Class

WBVar01729839NamePublic_nameWBVar01729839
Other_namecewivar00428364
B0496.12:n.42A>G
B0496.3e.1:c.710-211T>C
B0496.3h.1:c.-8-211T>C
B0496.19:n.249T>C
B0496.3g.1:c.-8-211T>C
B0496.3d.1:c.-8-211T>C
B0496.3a.1:c.-8-211T>C
HGVSgCHROMOSOME_IV:g.7428715T>C
Sequence_detailsSMapS_parentSequenceB0496
Flanking_sequencesCATTATTATCATCGAGAGCCCCCACTTTCTTTCTTATATTTTCAAATTTCAATCGTTTAT
Mapping_targetB0496
Source_location225CHROMOSOME_IV74287047428704From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023139From_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
AffectsGeneWBGene00201851
WBGene00195793
WBGene00006814
TranscriptB0496.3e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0496.3e.1:c.710-211T>C
Intron_number6/34
B0496.12VEP_consequencenon_coding_transcript_exon_variant
VEP_impactMODIFIER
HGVScB0496.12:n.42A>G
cDNA_position42
Exon_number1/1
B0496.3h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0496.3h.1:c.-8-211T>C
Intron_number2/30
B0496.3d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0496.3d.1:c.-8-211T>C
Intron_number2/32
B0496.19VEP_consequencenon_coding_transcript_exon_variant
VEP_impactMODIFIER
HGVScB0496.19:n.249T>C
cDNA_position249
Exon_number1/1
B0496.3g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0496.3g.1:c.-8-211T>C
Intron_number2/31
B0496.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0496.3a.1:c.-8-211T>C
Intron_number5/32
MethodWGS_Flibotte