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WormBase Tree Display for Variation: WBVar01962129

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Name Class

WBVar01962129NamePublic_nameWBVar01962129
Other_namecewivar00687939
H14E04.2d.1:c.390-50_390-49insAT
H14E04.2c.1:c.777-50_777-49insAT
H14E04.2b.1:c.765-50_765-49insAT
H14E04.2a.1:c.756-50_756-49insAT
HGVSgCHROMOSOME_III:g.2380715_2380716insAT
Sequence_detailsSMapS_parentSequenceH14E04
Flanking_sequencesAGAAATTTTTTTCGATTTTTTGAATTTTCAATTTTTTTTTCAAATTTTTAGAACGTTGAA
Mapping_targetH14E04
Source_location225CHROMOSOME_III23807052380706From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionAT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisMillion_mutation_project_reanalysis
WBStrain00022852From_analysisMillion_mutation_project_reanalysis
WBStrain00022856From_analysisMillion_mutation_project_reanalysis
WBStrain00022902From_analysisMillion_mutation_project_reanalysis
WBStrain00023191From_analysisMillion_mutation_project_reanalysis
WBStrain00023192From_analysisMillion_mutation_project_reanalysis
WBStrain00023286From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00019199
TranscriptH14E04.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2a.1:c.756-50_756-49insAT
Intron_number6/11
H14E04.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2c.1:c.777-50_777-49insAT
Intron_number7/12
H14E04.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2b.1:c.765-50_765-49insAT
Intron_number6/11
H14E04.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2d.1:c.390-50_390-49insAT
Intron_number3/8
MethodWGS_Flibotte