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: WBVar01771008

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01771008NamePublic_nameWBVar01771008
Other_namecewivar00471411
H14E04.2b.1:c.494-220C>T
H14E04.2d.1:c.119-220C>T
H14E04.2c.1:c.506-220C>T
H14E04.2a.1:c.485-220C>T
HGVSgCHROMOSOME_III:g.2379378C>T
Sequence_detailsSMapS_parentSequenceH14E04
Flanking_sequencesTACGCAAACACCGTCTCTTCGGTGTTTGCGACTTGTCACGGTACAGTAACCCAAAAGCTT
Mapping_targetH14E04
Source_location225CHROMOSOME_III23793682379368From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022852From_analysisMillion_mutation_project_reanalysis
WBStrain00022856From_analysisMillion_mutation_project_reanalysis
WBStrain00022886From_analysisMillion_mutation_project_reanalysis
WBStrain00022902From_analysisMillion_mutation_project_reanalysis
WBStrain00023191From_analysisMillion_mutation_project_reanalysis
WBStrain00023192From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00019199
TranscriptH14E04.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2a.1:c.485-220C>T
Intron_number5/11
H14E04.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2c.1:c.506-220C>T
Intron_number6/12
H14E04.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2b.1:c.494-220C>T
Intron_number5/11
H14E04.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2d.1:c.119-220C>T
Intron_number2/8
MethodWGS_Flibotte