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WormBase Tree Display for Variation: WBVar01571765

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Name Class

WBVar01571765NamePublic_nameWBVar01571765
Other_namecewivar00158196
F16H9.1d.1:c.268-44A>T
F16H9.1b.1:c.310-44A>T
F16H9.2b.1:c.35-19989T>A
F16H9.2a.1:c.-23-19989T>A
F16H9.1c.1:c.253-44A>T
F16H9.1a.1:c.274-44A>T
HGVSgCHROMOSOME_X:g.12727292A>T
Sequence_detailsSMapS_parentSequenceF22E10
Flanking_sequencesCATTTCATCAAACATGTTATTTTCACACACCACACACACACACATTCTAAAGGTTTCATA
Mapping_targetF22E10
Source_location225CHROMOSOME_X1272722212727222From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004600From_analysisMillion_mutation_project_reanalysis
WBStrain00022899From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00008901
WBGene00004345
TranscriptF16H9.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF16H9.1a.1:c.274-44A>T
Intron_number5/6
F16H9.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF16H9.2b.1:c.35-19989T>A
Intron_number1/3
F16H9.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF16H9.1d.1:c.268-44A>T
Intron_number5/6
F16H9.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF16H9.1c.1:c.253-44A>T
Intron_number5/6
F16H9.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF16H9.2a.1:c.-23-19989T>A
Intron_number1/4
F16H9.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF16H9.1b.1:c.310-44A>T
Intron_number5/6
MethodWGS_Flibotte