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WormBase Tree Display for Variation: WBVar01729845

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Name Class

WBVar01729845NamePublic_nameWBVar01729845
Other_name (11)
HGVSgCHROMOSOME_IV:g.7436639G>A
Sequence_detailsSMapS_parentSequenceB0496
Flanking_sequencesATTCTTTTTTCAAAATTCCTATTATCCTGTAATGTTTTCAGGTTGGATTTGATCCTGACG
Mapping_targetB0496
Source_location225CHROMOSOME_IV74366287436628From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGA
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
AffectsGeneWBGene00006814
TranscriptB0496.3h.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0496.3h.2:c.1897-12G>A
Intron_number9/27
B0496.3a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0496.3a.2:c.1897-12G>A
Intron_number10/27
B0496.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0496.3b.1:c.1897-12G>A
Intron_number9/30
B0496.3i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0496.3i.1:c.1948-12G>A
Intron_number9/29
B0496.3g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0496.3g.1:c.1897-12G>A
Intron_number12/31
B0496.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0496.3a.1:c.1897-12G>A
Intron_number15/32
B0496.3e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0496.3e.1:c.2614-12G>A
Intron_number15/34
B0496.3f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0496.3f.1:c.1897-12G>A
Intron_number9/28
B0496.3h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0496.3h.1:c.1897-12G>A
Intron_number12/30
B0496.3d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0496.3d.1:c.1897-12G>A
Intron_number12/32
MethodWGS_Flibotte