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WormBase Tree Display for Variation: WBVar01553141

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Name Class

WBVar01553141NamePublic_nameWBVar01553141
Other_namecewivar00130427
T04C10.4.1:c.274-89A>G
T04C10.11.1:c.*314-89A>G
T04C10.11.2:c.*749A>G
HGVSgCHROMOSOME_X:g.14809833T>C
Sequence_detailsSMapS_parentSequenceT04C10
Flanking_sequencesGAATTGTTTTTTTAAAGTTTCAGTCAAATTCAAAAGACTTCCAGAGGATTGCAACTCAAA
Mapping_targetT04C10
Source_location225CHROMOSOME_X1480976414809764From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004599From_analysisMillion_mutation_project_reanalysis
WBStrain00006631From_analysisMillion_mutation_project_reanalysis
WBStrain00022886From_analysisMillion_mutation_project_reanalysis
WBStrain00023138From_analysisMillion_mutation_project_reanalysis
WBStrain00023286From_analysisMillion_mutation_project_reanalysis
WBStrain00023665From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00303075
WBGene00000221
TranscriptT04C10.11.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT04C10.11.1:c.*314-89A>G
Intron_number4/4
T04C10.4.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT04C10.4.1:c.274-89A>G
Intron_number2/4
T04C10.11.2VEP_consequence3_prime_UTR_variant
VEP_impactMODIFIER
HGVScT04C10.11.2:c.*749A>G
cDNA_position934
Exon_number4/4
MethodWGS_Flibotte