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WormBase Tree Display for Variation: WBVar01546845

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Name Class

WBVar01546845NamePublic_nameWBVar01546845
Other_namecewivar00121432
C09G5.8a.1:c.1190+601G>T
C09G5.14.1:c.112C>A
C09G5.8b.1:c.500+601G>T
CE52105:p.His38Asn
HGVSgCHROMOSOME_II:g.10723058G>T
Sequence_detailsSMapS_parentSequenceC09G5
Flanking_sequencesACATCATGAAATCTGCCATTTTCCGAGCATCTCATCAAGACATGATTTCTGATGAACATT
Mapping_targetC09G5
Source_location225CHROMOSOME_II1072299910722999From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004599From_analysisMillion_mutation_project_reanalysis
WBStrain00004600From_analysisMillion_mutation_project_reanalysis
WBStrain00006629From_analysisMillion_mutation_project_reanalysis
WBStrain00006631From_analysisMillion_mutation_project_reanalysis
WBStrain00006640From_analysisMillion_mutation_project_reanalysis
WBStrain00022878From_analysisMillion_mutation_project_reanalysis
WBStrain00023138From_analysisMillion_mutation_project_reanalysis
WBStrain00027647From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00271803
WBGene00007490
TranscriptC09G5.8a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09G5.8a.1:c.1190+601G>T
Intron_number7/18
C09G5.8b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC09G5.8b.1:c.500+601G>T
Intron_number2/12
C09G5.14.1 (12)
MethodWGS_Flibotte