Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Variation: WBVar01994654

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01994654NamePublic_nameWBVar01994654
Other_namecewivar00721917
H14E04.2b.1:c.494-1136_494-1135insG
H14E04.2a.1:c.485-1136_485-1135insG
H14E04.2c.1:c.506-1136_506-1135insG
H14E04.2d.1:c.119-1136_119-1135insG
HGVSgCHROMOSOME_III:g.2378462_2378463insG
Sequence_detailsSMapS_parentSequenceH14E04
Flanking_sequencesATAAATTTCGTGACTCATGTGCTTCTACTCGTATTGATTGCAGTAAAAACTGTATTTATTCACATTTTTAGCACTAAATT
Mapping_targetH14E04
Source_location225CHROMOSOME_III23784522378453From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006629From_analysisMillion_mutation_project_reanalysis
WBStrain00006631From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
WBStrain00024204From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00019199
TranscriptH14E04.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2a.1:c.485-1136_485-1135insG
Intron_number5/11
H14E04.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2c.1:c.506-1136_506-1135insG
Intron_number6/12
H14E04.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2b.1:c.494-1136_494-1135insG
Intron_number5/11
H14E04.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2d.1:c.119-1136_119-1135insG
Intron_number2/8
MethodWGS_Flibotte