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WormBase Tree Display for Variation: WBVar01551601

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Name Class

WBVar01551601NamePublic_nameWBVar01551601
Other_namecewivar00128658
T06H11.1e.1:c.-25T>G
T06H11.1c.1:c.149-1832T>G
T06H11.1b.1:c.263-1832T>G
T06H11.1g.1:c.137-1832T>G
T06H11.1d.1:c.293-1832T>G
T06H11.1f.1:c.413-1832T>G
HGVSgCHROMOSOME_X:g.10111163A>C
Sequence_detailsSMapS_parentSequenceT06H11
Flanking_sequencesGACCATCGAGAAGAAGTGTTTTCATTTAAATGGAGCAACAACCCTTGGGGTGCAAGGTGC
Mapping_targetT06H11
Source_location225CHROMOSOME_X1011110410111104From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004599From_analysisMillion_mutation_project_reanalysis
WBStrain00022850From_analysisMillion_mutation_project_reanalysis
WBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00023192From_analysisMillion_mutation_project_reanalysis
WBStrain00024204From_analysisMillion_mutation_project_reanalysis
WBStrain00027647From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006792
TranscriptT06H11.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1b.1:c.263-1832T>G
Intron_number3/12
T06H11.1g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1g.1:c.137-1832T>G
Intron_number2/12
T06H11.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1f.1:c.413-1832T>G
Intron_number4/14
T06H11.1e.1VEP_consequence5_prime_UTR_variant
VEP_impactMODIFIER
HGVScT06H11.1e.1:c.-25T>G
cDNA_position58
Exon_number1/14
T06H11.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1d.1:c.293-1832T>G
Intron_number1/11
T06H11.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1c.1:c.149-1832T>G
Intron_number2/13
MethodWGS_Flibotte