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WormBase Tree Display for Variation: WBVar01565626

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Name Class

WBVar01565626NamePublic_nameWBVar01565626
Other_namecewivar00148925
H14E04.2c.1:c.352+60T>C
H14E04.2a.1:c.352+60T>C
H14E04.2b.1:c.361+60T>C
HGVSgCHROMOSOME_III:g.2376751T>C
Sequence_detailsSMapS_parentSequenceH14E04
Flanking_sequencesTGACCCGGAAACGTTTGAGCCTGAAAAAAAGACTGAAAACTGAGAAAGAGTTATTTTTTT
Mapping_targetH14E04
Source_location225CHROMOSOME_III23767412376741From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004600From_analysisMillion_mutation_project_reanalysis
WBStrain00004602From_analysisMillion_mutation_project_reanalysis
WBStrain00006629From_analysisMillion_mutation_project_reanalysis
WBStrain00006631From_analysisMillion_mutation_project_reanalysis
WBStrain00006637From_analysisMillion_mutation_project_reanalysis
WBStrain00023018From_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.352+60T>C
Intron_number4/11
H14E04.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2c.1:c.352+60T>C
Intron_number4/12
H14E04.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2b.1:c.361+60T>C
Intron_number4/11
MethodWGS_Flibotte