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WormBase Tree Display for Variation: WBVar01771006

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Name Class

WBVar01771006NamePublic_nameWBVar01771006
Other_namecewivar00471409
H14E04.2b.1:c.176-7C>T
H14E04.2a.1:c.176-16C>T
H14E04.2c.1:c.176-16C>T
HGVSgCHROMOSOME_III:g.2376499C>T
Sequence_detailsSMapS_parentSequenceH14E04
Flanking_sequencesCACTAAAACTTGATTAAAAATTCCCAATTTTCCCAGTTTTTTCAGAGTCAACCGCCGATG
Mapping_targetH14E04
Source_location225CHROMOSOME_III23764892376489From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022852From_analysisMillion_mutation_project_reanalysis
WBStrain00022856From_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.176-16C>T
Intron_number3/11
H14E04.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2c.1:c.176-16C>T
Intron_number3/12
H14E04.2b.1VEP_consequencesplice_region_variant,intron_variant
VEP_impactLOW
HGVScH14E04.2b.1:c.176-7C>T
Intron_number3/11
MethodWGS_Flibotte